* [Lexogen's Online FAQs](https://faqs.lexogen.com/faq.md)
* [Products labeling](https://faqs.lexogen.com/faq/a-guide-to-our-new-product-labels.md)
* [A lot of my reads are not mapped (reads too short). Is there anything I can do to map shorter reads?](https://faqs.lexogen.com/faq/a-lot-of-my-reads-are-not-mapped-reads-too-short-i.md)
* [Why do I observe some ribosomal peaks after poly(A) selection?](https://faqs.lexogen.com/faq/after-poly-a-selection-bioanalyzer-still-detects-s.md)
* [All about Samples: requirements, preparation, submission and shipment](https://faqs.lexogen.com/faq/all-about-samples-requirements-preparation-submiss.md)
* [Are my libraries overcycled? If so, what should I do?](https://faqs.lexogen.com/faq/are-my-libraries-overcycled-what-should-i-do.md)
* [Are the data comparable between QuantSeq REV V1 and V2?](https://faqs.lexogen.com/faq/are-the-data-comparable-between-quantseq-rev-v1-an.md)
* [Are the data obtained with QuantSeq with UDI V1 and V2 comparable?](https://faqs.lexogen.com/faq/are-the-data-obtained-with-quantseq-with-udi-v1-an.md)
* [Are the long SIRVs (Set 4) also isoforms of a given gene?](https://faqs.lexogen.com/faq/are-the-long-sirvs-also-isoforms-of-a-given-gene-s.md)
* [Are the reagents interchangeable between miRVEL Discovery and Profiling?](https://faqs.lexogen.com/faq/are-the-reagents-interchangeable-between-mirvel-di.md)
* [Are the UDI V2 Add-on kits compatible with libraries of other vendors?](https://faqs.lexogen.com/faq/are-the-udi-v2-add-on-kits-compatible-with-librari.md)
* [Are there any sample types that are not compatible with the RNA/DNA Defender Solution?](https://faqs.lexogen.com/faq/are-there-any-sample-types-that-are-not-compatible.md)
* [Are there recommendations for low RNA input?](https://faqs.lexogen.com/faq/are-there-recommendations-for-low-rna-input.md)
* [Are there recommendations for low RNA input and serum/plasma samples?](https://faqs.lexogen.com/faq/are-there-recommendations-for-low-rna-input-and-se.md)
* [Are there some additional instructions for how to run the HPLC analysis for the S4U Incorporation assay (e.g. Column, temperature, injection volume, and flow rate)?](https://faqs.lexogen.com/faq/are-there-some-additional-instructions-for-how-to-.md)
* [Are there specific recommendations for demultiplexing QuantSeq FFPE using bcl2fastq?](https://faqs.lexogen.com/faq/are-there-specific-recommendations-for-demultiplex.md)
* [Are Unique Molecular Identifiers (UMIs) included in QuantSeq FFPE?](https://faqs.lexogen.com/faq/are-unique-molecular-identifiers-umis-included-in-.md)
* [AVITI Loading Guidelines- CloudBreak Freestyle 2025](https://faqs.lexogen.com/faq/aviti-loading-guidelines.md)
* [BC1 Block Module for QuantSeq](https://faqs.lexogen.com/faq/bc1-block-module-for-quantseq.md)
* [Can cells be fixed and then processed with LUTHOR HD?](https://faqs.lexogen.com/faq/can-cells-be-fixed-and-then-processed-with-luthor-.md)
* [Can cells be frozen and stored in the Cell Lysis Buffer?](https://faqs.lexogen.com/faq/can-cells-be-frozen-and-stored-in-the-cell-lysis-b.md)
* [Can Globin Block be used with input amounts below 50 ng?](https://faqs.lexogen.com/faq/can-globin-block-be-used-with-input-amounts-below-.md)
* [Can Globin Block Modules be used with low quality RNA?](https://faqs.lexogen.com/faq/can-globin-block-modules-be-used-with-low-quality-.md)
* [Can I add blocking oligos to prevent the second strand synthesis of high abundant RNAs?](https://faqs.lexogen.com/faq/can-i-add-blocking-oligos-to-prevent-the-second-st.md)
* [Can I always replace QuantSeq FWD with QuantSeq-Pool?](https://faqs.lexogen.com/faq/can-i-always-replace-standard-quantseq-with-quants.md)
* [Can I analyze my MGI data on Kangooroo?](https://faqs.lexogen.com/faq/can-i-analyze-my-mgi-data-on-kangooroo.md)
* [How can I analyze my QuantSeq data?](https://faqs.lexogen.com/faq/can-i-analyze-my-quantseq-data-using-the-data-anal.md)
* [How can I analyze my QuantSeq with UDI V2 data?](https://faqs.lexogen.com/faq/can-i-analyze-my-quantseq-with-udi-v2-data-using-t.md)
* [Can I buy the Elution Buffer (EB) separately?](https://faqs.lexogen.com/faq/can-i-buy-the-elution-buffer-eb-separately.md)
* [Can I choose the sequencing depth and read length?](https://faqs.lexogen.com/faq/can-i-choose-the-sequencing-depth-and-read-length.md)
* [Can I expect changes in the expression of other transcripts when depleting BC1?](https://faqs.lexogen.com/faq/can-i-expect-changes-in-the-expression-of-other-tr.md)
* [Can I extract DNA with the SPLIT Kit?](https://faqs.lexogen.com/faq/can-i-extract-dna-with-the-split-kit.md)
* [Can I extract the RNA downstream of TraPR with methods other than phenol-chloroform, e.g. with TRIzol or silica spin-columns?](https://faqs.lexogen.com/faq/can-i-extract-the-rna-downstream-of-trapr-with-met.md)
* [Can I get script files for QuantSeq automation?](https://faqs.lexogen.com/faq/can-i-get-script-files-for-quantseq-automation.md)
* [Can I install the automated protocol myself?](https://faqs.lexogen.com/faq/can-i-install-the-automated-protocol-myself.md)
* [Can I merge my FASTQ files on Kangooroo?](https://faqs.lexogen.com/faq/can-i-merge-my-fastq-files-on-kangooroo.md)
* [Can I pool Lexogen libraries with other library types in the same lanemix for sequencing?](https://faqs.lexogen.com/faq/can-i-pool-lexogen-libraries-with-other-library-ty.md)
* [Can I reamplify my libraries using the PCR and Reamplification Add-on Kit?](https://faqs.lexogen.com/faq/can-i-reamplify-my-libraries-using-the-pcr-add-on-.md)
* [Can I receive the remaining sample (RNA, cells, tissues) after it has been submitted for services?](https://faqs.lexogen.com/faq/can-i-receive-the-remaining-sample-rna-cells-tissu.md)
* [Can I run the protocol without thermomixer?](https://faqs.lexogen.com/faq/can-i-run-the-protocol-without-thermomixer.md)
* [Can I sequence my miRVEL Small RNA-Seq libraries if the concentration is lower than the recommended 4 nM?](https://faqs.lexogen.com/faq/can-i-sequence-the-mirvel-discovery-small-rna-seq-.md)
* [Can I ship samples from any country?](https://faqs.lexogen.com/faq/can-i-ship-samples-from-any-country.md)
* [Can I split my Kangooroo voucher into multiple vouchers?](https://faqs.lexogen.com/faq/can-i-split-my-kangooroo-voucher-into-multiple-vou.md)
* [Can I store SIRV dilutions for further use?](https://faqs.lexogen.com/faq/can-i-store-sirv-dilutions-for-further-use.md)
* [Can I use custom primers for reverse transcription or PCR?](https://faqs.lexogen.com/faq/can-i-use-custom-primers-for-reverse-transcription.md)
* [Can I use low quality RNA as input for TeloPrime Full-Length cDNA Amplification?](https://faqs.lexogen.com/faq/can-i-use-low-quality-rna-as-input-for-teloprime-f.md)
* [Can I use other fluorophores instead of SYBR Green?](https://faqs.lexogen.com/faq/can-i-use-other-fluorophores-instead-of-sybr-green.md)
* [Can I use paired-end sequencing for QuantSeq FWD libraries?](https://faqs.lexogen.com/faq/can-i-use-paired-end-sequencing-for-quantseq-fwd-l.md)
* [Can I use paired-end sequencing for QuantSeq REV libraries?](https://faqs.lexogen.com/faq/can-i-use-paired-end-sequencing-for-quantseq-rev-l.md)
* [Can I use QuantSeq-Flex with the QuantSeq REV 2 Version?](https://faqs.lexogen.com/faq/can-i-use-quantseq-flex-with-the-quantseq-rev-vers.md)
* [Can I use RiboCop in combination with the CORALL Total RNA-Seq Kit?](https://faqs.lexogen.com/faq/can-i-use-ribocop-in-combination-with-the-corall-t.md)
* [Can I use RTL with FFPE/low quality samples?](https://faqs.lexogen.com/faq/can-i-use-rtl-with-ffpe-low-quality-samples.md)
* [Can I use sample barcodes for multiplexing TeloPrime cDNA for NGS applications?](https://faqs.lexogen.com/faq/can-i-use-sample-barcodes-for-multiplexing-telopri.md)
* [Can I use sample barcodes or UMIs for targeted sequencing?](https://faqs.lexogen.com/faq/can-i-use-sample-barcodes-or-umis-for-targeted-seq.md)
* [Can I use single read sequencing for QuantSeq FFPE?](https://faqs.lexogen.com/faq/can-i-use-single-read-sequencing-for-quantseq-ffpe.md)
* [Can I use single-read sequencing for QuantSeq-Pool libraries?](https://faqs.lexogen.com/faq/can-i-use-single-read-sequencing-for-quantseq-pool.md)
* [Can I use SPLIT to obtain small and large RNA-enriched fractions from already extracted RNA?](https://faqs.lexogen.com/faq/can-i-use-split-to-separate-small-and-large-rna-fr.md)
* [Can I use the enzyme from the PCR Add-on kit to perform QuantSeq-Pool Endpoint PCR?](https://faqs.lexogen.com/faq/can-i-use-the-enzyme-from-the-pcr-add-on-kit-to-pe.md)
* [Can I use the purified RISC fraction for downstream biochemical analyses?](https://faqs.lexogen.com/faq/can-i-use-the-purified-risc-fraction-for-downstrea.md)
* [Can I use TraPR for FFPE samples?](https://faqs.lexogen.com/faq/can-i-use-trapr-for-ffpe-samples.md)
* [Can I use TraPR with low RNA-containing bio-fluids such as plasma?](https://faqs.lexogen.com/faq/can-i-use-trapr-with-low-rna-containing-bio-fluids.md)
* [Can I use UDIs from other Lexogen´s kits?](https://faqs.lexogen.com/faq/can-i-use-udis-from-other-lexogen-s-kits.md)
* [Can I use the UMIs module with QuantSeq-Flex libraries?](https://faqs.lexogen.com/faq/can-i-use-umis-for-quantseq-flex-libraries.md)
* [Can indices provided with other Lexogen library prep kits be used for small RNA library preparation?](https://faqs.lexogen.com/faq/can-indices-provided-with-other-lexogen-library-pr.md)
* [Can libraries be submitted for sequencing only?](https://faqs.lexogen.com/faq/can-libraries-be-submitted-for-sequencing-only.md)
* [Can Mix² be used to find differentially expressed genes isoforms?](https://faqs.lexogen.com/faq/can-mix2-be-used-to-find-differentially-expressed-.md)
* [Can plant and bacterial rRNA be co-depleted with RiboCop?](https://faqs.lexogen.com/faq/can-plant-and-bacterial-rrna-be-co-depleted-with-r.md)
* [Can reagents between QuantSeq FFPE and QuantSeq V2 kits be exchanged?](https://faqs.lexogen.com/faq/can-reagents-between-quantseq-ffpe-and-quantseq-v2.md)
* [Can RiboCop be used for RiboSeq applications / to retain small RNA fragments?](https://faqs.lexogen.com/faq/can-ribocop-be-used-for-riboseq-applications-to-re.md)
* [Can SLAMseq be used for analyzing nascent expression levels and kinetics of small RNAs?](https://faqs.lexogen.com/faq/can-slamseq-be-used-for-analyzing-nascent-expressi.md)
* [Can the BC1 Block and Globin Block Modules be used with QuantSeq REV V2?](https://faqs.lexogen.com/faq/can-the-bc1-block-and-globin-block-modules-be-used.md)
* [Can the BC1 Block Module be used with low quality RNA input?](https://faqs.lexogen.com/faq/can-the-bc1-block-module-be-used-with-low-quality-.md)
* [Can the META Probe Mix be used with monoculture samples?](https://faqs.lexogen.com/faq/can-the-meta-probe-mix-be-used-with-monoculture-sa.md)
* [Can the Probe Mixes from different RiboCop kits be used in combination for a one-step rRNA co-depletion?](https://faqs.lexogen.com/faq/can-the-probe-mixes-from-different-ribocop-kits-be.md)
* [Can the SPLIT Kit be used to extract RNA from plasma samples?](https://faqs.lexogen.com/faq/can-the-split-kit-be-used-to-extract-rna-from-plas.md)
* [Can this kit be used with other library preps?](https://faqs.lexogen.com/faq/can-this-kit-be-used-with-other-library-preps.md)
* [Can UMIs be included in QuantSeq-REV V2 libraries?](https://faqs.lexogen.com/faq/can-umis-be-included-in-quantseq-rev-v2-libraries.md)
* [Can you prepare small RNA and total RNA libraries from the same RNA sample?](https://faqs.lexogen.com/faq/can-you-prepare-small-rna-and-total-rna-libraries-.md)
* [CORALL Analysis](https://faqs.lexogen.com/faq/corall-analysis.md)
* [CORALL Blood RNA-Seq](https://faqs.lexogen.com/faq/corall-blood-rna-seq.md)
* [CORALL FFPE RNA-Seq](https://faqs.lexogen.com/faq/corall-ffpe-rna-seq.md)
* [CORALL mRNA-Seq V2](https://faqs.lexogen.com/faq/corall-mrna-seq-v2.md)
* [CORALL](https://faqs.lexogen.com/faq/corall-rna-seq-library-prep-kits.md)
* [CORALL Total RNA-Seq V2](https://faqs.lexogen.com/faq/corall-total-rna-seq-v2.md)
* [CORALL V2 General](https://faqs.lexogen.com/faq/corall-v2-general.md)
* [Data analysis, reports, & data transfer](https://faqs.lexogen.com/faq/data-analysis-reports-data-transfer.md)
* [Data Analysis](https://faqs.lexogen.com/faq/data-analysis-solutions.md)
* [Do I have enough cycles of SBS chemistry in my NovaSeq Reagent Kit v1.5 to read out the full 12 nt length of Lexogen UDIs?](https://faqs.lexogen.com/faq/do-i-have-enough-cycles-of-sbs-chemistry-in-my-nov.md)
* [Do I need an on-deck thermocycler?](https://faqs.lexogen.com/faq/do-i-need-an-on-deck-thermocycler.md)
* [Do I need any extra reagents to purify the sRNAs?](https://faqs.lexogen.com/faq/do-i-need-any-extra-reagents-to-purify-the-srnas.md)
* [Do I need any special equipment to use TraPR?](https://faqs.lexogen.com/faq/do-i-need-any-special-equipment-to-use-trapr.md)
* [Do I need multiple rounds of poly(A) selection?](https://faqs.lexogen.com/faq/do-i-need-multiple-rounds-of-poly-a-selection.md)
* [Do I need special de-multiplexing software tools for this product?](https://faqs.lexogen.com/faq/do-i-need-special-de-multiplexing-software-tools-f.md)
* [Do I need the PCR Add-on Kit for performing the qPCR assay?](https://faqs.lexogen.com/faq/do-i-need-the-pcr-add-on-kit-for-performing-the-qp.md)
* [Do I need to change S4U-containing medium every 3 hours?](https://faqs.lexogen.com/faq/do-i-need-to-change-s4u-containing-medium-every-3-.md)
* [Do I need to get all 4 modules or can I just get the kinetics kit(s)?](https://faqs.lexogen.com/faq/do-i-need-to-get-all-4-modules-or-can-i-just-get-t.md)
* [Do I need to get both the First Strand Synthesis Flex Module V2 and the Second Strand Synthesis Module?](https://faqs.lexogen.com/faq/do-i-need-to-get-both-the-first-strand-synthesis-f.md)
* [Do I need to perform a DNAse I treatment on my RNA samples?](https://faqs.lexogen.com/faq/do-i-need-to-perform-a-dnase-i-treatment-on-my-rna.md)
* [Do I need to perform a qPCR assay to determine the number of PCR cycles for the EP PCR?](https://faqs.lexogen.com/faq/do-i-need-to-perform-a-qpcr-assay-to-determine-the.md)
* [Do I need to purchase additional kits, e.g., for purification ?](https://faqs.lexogen.com/faq/do-i-need-to-purchase-additional-kits-e-g-for-pu-1.md)
* [Do I need to purchase additional kits, e.g., for purification?](https://faqs.lexogen.com/faq/do-i-need-to-purchase-additional-kits-e-g-for-puri.md)
* [Do I need to purchase any additional modules or reagents for an efficient rRNA depletion with RiboCop?](https://faqs.lexogen.com/faq/do-i-need-to-purchase-any-additional-modules-or-re.md)
* [Do I need to purchase any extra reagents to perform the extraction?](https://faqs.lexogen.com/faq/do-i-need-to-purchase-any-extra-reagents-to-perf-1.md)
* [Do I still need to add UDIs to my libraries when using UMIs ?](https://faqs.lexogen.com/faq/do-i-still-need-to-add-i5-and-i7-indices-to-my-lib.md)
* [Do miRVEL Discovery sRNA-Seq libraries contain hY4 Y reads?](https://faqs.lexogen.com/faq/do-mirvel-discovery-srna-seq-libraries-contain-hy4.md)
* [Do my BC1 Block libraries look okay?](https://faqs.lexogen.com/faq/do-my-bc1-block-libraries-look-okay.md)
* [Do my Globin Block libraries look okay?](https://faqs.lexogen.com/faq/do-my-globin-block-libraries-look-okay.md)
* [Do my QuantSeq FWD-UMI reads look okay?](https://faqs.lexogen.com/faq/do-my-quantseq-fwd-umi-reads-look-okay.md)
* [Do you also offer DNA-Seq Services?](https://faqs.lexogen.com/faq/do-you-also-offer-dna-seq-services.md)
* [Do you have a list of publications featuring QuantSeq on plants?](https://faqs.lexogen.com/faq/do-you-have-a-list-of-publications-featuring-quant.md)
* [Do you have any protocol recommendations to get longer insert sizes?](https://faqs.lexogen.com/faq/do-you-have-any-protocol-recommendations-to-get-lo.md)
* [Do you have any recommendations for RNA extractions? What about for serum and plasma samples?](https://faqs.lexogen.com/faq/do-you-have-any-recommendations-for-rna-extracti-1.md)
* [Do you have any recommendations for RNA extractions?](https://faqs.lexogen.com/faq/do-you-have-any-recommendations-for-rna-extraction.md)
* [Do you have any specific recommendations for FFPE SPLIT RNA columns preparation?](https://faqs.lexogen.com/faq/do-you-have-any-specific-recommendations-for-ffpe-.md)
* [Do you have any tips for magnetic bead purification?](https://faqs.lexogen.com/faq/do-you-have-any-tips-for-magnetic-bead-purificatio.md)
* [Do you have guidelines for the optimal S4U concentrations to use for different cell lines?](https://faqs.lexogen.com/faq/do-you-have-guidelines-for-the-optimal-s4u-concent.md)
* [Do you have some publications featuring QuantSeq with Globin Block?](https://faqs.lexogen.com/faq/do-you-have-some-publications-featuring-quantseq-w.md)
* [Do you have UMIs for Small RNA-Seq libraries?](https://faqs.lexogen.com/faq/do-you-have-umis-for-small-rna-seq-libraries.md)
* [Does LUTHOR HD replace 10X Genomics Data?](https://faqs.lexogen.com/faq/does-luthor-hd-replace-10x-genomics-data.md)
* [Does Mix² accept both single-end and paired-end read alignments?](https://faqs.lexogen.com/faq/does-mix2-accept-both-single-end-and-paired-end-re.md)
* [Does Mix² support multi cores?](https://faqs.lexogen.com/faq/does-mix2-support-multi-cores.md)
* [Does RiboCop for Plants efficiently deplete rRNA from low quality RNA?](https://faqs.lexogen.com/faq/does-ribocop-for-plants-efficiently-deplete-rrna-f.md)
* [Does RiboCop for Yeast efficiently deplete rRNA from low quality RNA?](https://faqs.lexogen.com/faq/does-ribocop-for-yeast-efficiently-deplete-rrna-fr.md)
* [For which organisms are you providing Services?](https://faqs.lexogen.com/faq/for-which-organisms-are-you-providing-services.md)
* [For which RNA-Seq applications are you offering services?](https://faqs.lexogen.com/faq/for-which-rna-seq-applications-are-you-offering-se.md)
* [Data Analysis results](https://faqs.lexogen.com/faq/general-data-analysis.md)
* [General guidelines for good scientific practice for NGS workflows](https://faqs.lexogen.com/faq/general-guidelines-for-good-scientific-practice-fo.md)
* [General Guidelines for Lexogen Kit Use](https://faqs.lexogen.com/faq/general-guidelines-for-lexogen-kit-use.md)
* [General information](https://faqs.lexogen.com/faq/general-information.md)
* [General FAQs](https://faqs.lexogen.com/faq/general-product-and-technical-faqs.md)
* [Globin Block Modules for QuantSeq](https://faqs.lexogen.com/faq/globin-block-modules-for-quantseq.md)
* [How are my CORALL data analyzed with Kangooroo?](https://faqs.lexogen.com/faq/how-are-my-corall-data-analyzed-with-kangooroo.md)
* [How are my miRVEL data analyzed with Kangooroo?](https://faqs.lexogen.com/faq/how-are-my-mirvel-data-analyzed-with-kangooroo-.md)
* [How are my QuantSeq and LUTHOR HD data analyzed with Kangooroo?](https://faqs.lexogen.com/faq/how-are-my-quantseq-data-analyzed-with-kangooroo.md)
* [How are my WTS data analyzed with Kangooroo?](https://faqs.lexogen.com/faq/how-are-my-wts-data-analyzed-with-kangooroo-.md)
* [How are the 5’ and 3’ ends tagged?](https://faqs.lexogen.com/faq/how-are-the-5-and-3-ends-tagged.md)
* [How are the SIRV transcripts and isoform mixes produced?](https://faqs.lexogen.com/faq/how-are-the-sirv-isoform-mixes-produced.md)
* [How are the SIRV isoforms designed?](https://faqs.lexogen.com/faq/how-are-the-sirv-isoforms-designed.md)
* [How are UMIs read-out during sequencing? What read length is needed?](https://faqs.lexogen.com/faq/how-are-umis-read-out-during-sequencing-what-read-.md)
* [How can I add UMIs to my QuantSeq FWD libraries?](https://faqs.lexogen.com/faq/how-can-i-add-umis-to-my-quantseq-libraries.md)
* [How can I analyze my QuantSeq FFPE data?](https://faqs.lexogen.com/faq/how-can-i-analyze-my-quantseq-ffpe-data.md)
* [How can I analyze my QuantSeq-REV V2 data?](https://faqs.lexogen.com/faq/how-can-i-analyze-my-quantseq-rev-v2-data.md)
* [How can I analyze my Small RNA sequencing data?](https://faqs.lexogen.com/faq/how-can-i-analyze-my-small-rna-sequencing-data.md)
* [How can I analyze my miRVEL Small RNA sequencing data ?](https://faqs.lexogen.com/faq/how-can-i-analyze-my-small-rna-sequencing-data-1.md)
* [How can I analyze SIRVs?](https://faqs.lexogen.com/faq/how-can-i-analyze-sirvs.md)
* [How can I check for the presence of small RNAs before proceeding to library prep?](https://faqs.lexogen.com/faq/how-can-i-check-for-the-presence-of-small-rnas-bef.md)
* [How can I check the optimal PCR cycle number if I cannot perform the qPCR assay?](https://faqs.lexogen.com/faq/how-can-i-check-the-optimal-pcr-cycle-number-if-i-.md)
* [How can I determine the amount of globin mapping reads in my sequencing data?](https://faqs.lexogen.com/faq/how-can-i-determine-the-amount-of-globin-mapping-r.md)
* [How can I get updates on the project status?](https://faqs.lexogen.com/faq/how-can-i-get-updates-on-the-project-status.md)
* [How can I increase my final yield?](https://faqs.lexogen.com/faq/how-can-i-increase-my-final-yield.md)
* [How can I multiplex more than 384 samples on an Illumina NovaSeq instrument if you only offer 384 different UDIs?](https://faqs.lexogen.com/faq/how-can-i-multiplex-more-than-384-samples-on-an-il.md)
* [How can I perform error correction of Lexogen's 12 nt Unique Dual Indices?](https://faqs.lexogen.com/faq/how-can-i-perform-error-correction-of-udi-12-nt-un.md)
* [How can I QC my RNA after using RiboCop for Yeast?](https://faqs.lexogen.com/faq/how-can-i-qc-my-rna-after-using-ribocop-for-yeast.md)
* [How can I scale up the Poly(A) Selection reaction for input amounts higher than 5 µg?](https://faqs.lexogen.com/faq/how-can-i-scale-up-the-poly-a-selection-reaction-f.md)
* [How can I use SIRVs to measure the mRNA content of my sample?](https://faqs.lexogen.com/faq/how-can-i-use-sirvs-to-measure-the-mrna-content-of.md)
* [How can I use TeloPrime to prepare full-length cDNA for long-read sequencing applications?](https://faqs.lexogen.com/faq/how-can-i-use-teloprime-to-prepare-full-length-cdn.md)
* [How do I analyze my LUTHOR HD Pool data?](https://faqs.lexogen.com/faq/how-do-i-analyze-my-luthor-hd-pool-data.md)
* [How do I analyze my QuantSeq FWD-UMI Sequencing Data?](https://faqs.lexogen.com/faq/how-do-i-analyze-my-quantseq-fwd-umi-sequencing-da.md)
* [How can I analyze my QuantSeq-Pool data?](https://faqs.lexogen.com/faq/how-do-i-analyze-my-quantseq-pool-data-can-i-use-t.md)
* [How do I analyze my SLAMseq data?](https://faqs.lexogen.com/faq/how-do-i-analyze-my-slamseq-data.md)
* [How do I analyze the data from LUTHOR HD 3’ mRNA-Seq libraries?](https://faqs.lexogen.com/faq/how-do-i-analyze-the-data-from-luthor-hd-3-mrna-se.md)
* [How do I calculate endpoint cycle numbers?](https://faqs.lexogen.com/faq/how-do-i-calculate-endpoint-cycle-numbers.md)
* [How do I calculate the S4U Incorporation Rate?](https://faqs.lexogen.com/faq/how-do-i-calculate-the-s4u-incorporation-rate.md)
* [How do I choose the number of PCR cycles to use for library amplification ?](https://faqs.lexogen.com/faq/how-do-i-choose-the-number-of-pcr-cycles-to-use--1.md)
* [How do I choose the number of PCR cycles to use for library amplification?](https://faqs.lexogen.com/faq/how-do-i-choose-the-number-of-pcr-cycles-to-use-fo.md)
* [How to choose the right Lexogen UDI 12 nt Unique Dual Indexing set?](https://faqs.lexogen.com/faq/how-do-i-choose-the-right-lexogen-udi-12-nt-unique.md)
* [How do I download my results from the Kangooroo platform?](https://faqs.lexogen.com/faq/how-do-i-download-my-results-from-the-kangooroo-pl.md)
* [How do I fill in my sample file?](https://faqs.lexogen.com/faq/how-do-i-fill-in-my-sample-file.md)
* [How do I initiate a project with Lexogen NGS Services?](https://faqs.lexogen.com/faq/how-do-i-initiate-a-project-with-lexogen-ngs-servi.md)
* [How do I make a lane mix for sequencing?](https://faqs.lexogen.com/faq/how-do-i-make-a-lane-mix-for-sequencing.md)
* [How do I pre-warm the FS2 / E1 mastermix for automated library prep?](https://faqs.lexogen.com/faq/how-do-i-pre-warm-the-fs2-e1-mastermix-for-automat.md)
* [How do I select the optimal RiboCop for Bacteria Kit?](https://faqs.lexogen.com/faq/how-do-i-select-the-optimal-ribocop-for-bacteria-k.md)
* [How do I select the right SIRV spike-in set?](https://faqs.lexogen.com/faq/how-do-i-select-the-right-sirv-spike-in-set-.md)
* [How do I spike-in the SIRVs?](https://faqs.lexogen.com/faq/how-do-i-spike-in-the-sirvs.md)
* [How do I upload my files in the Kangooroo platform?](https://faqs.lexogen.com/faq/how-do-i-upload-my-files-in-the-kangooroo-platform.md)
* [Can I add new genome references for my data analysis with Kangooroo?](https://faqs.lexogen.com/faq/how-do-i-upload-new-genome-references-for-my-data-.md)
* [How do I use the i1 Demultiplexing tool?](https://faqs.lexogen.com/faq/how-do-i-use-the-i1-demultiplexing-tool.md)
* [How Does TeloPrime V2 perform for different types of RNA?](https://faqs.lexogen.com/faq/how-does-teloprime-v2-perform-for-different-types-.md)
* [How does TraPR achieve species-independent isolation of functional sRNAs?](https://faqs.lexogen.com/faq/how-does-trapr-achieve-species-independent-isolati.md)
* [How is genomic DNA removed with the SPLIT RNA Extraction Kit?](https://faqs.lexogen.com/faq/how-is-genomic-dna-removed-with-the-split-rna-extr.md)
* [How is Mix² different from other quantification tools?](https://faqs.lexogen.com/faq/how-is-mix2-different-from-other-quantification-to.md)
* [How is the cycle number of the endpoint PCR determined?](https://faqs.lexogen.com/faq/how-is-the-cycle-number-of-the-endpoint-pcr-determ.md)
* [How long and at what temperature can my samples be stored in the RNA/DNA Defender Solution?](https://faqs.lexogen.com/faq/how-long-and-at-what-temperature-can-my-samples-be.md)
* [How long are my data stored in Kangooroo?](https://faqs.lexogen.com/faq/how-long-are-my-data-stored-in-kangooroo.md)
* [How long are my voucher codes valid?](https://faqs.lexogen.com/faq/how-long-are-my-voucher-codes-valid.md)
* [How long are the SIRVs?](https://faqs.lexogen.com/faq/how-long-are-the-sirvs.md)
* [How long does it take to generate QuantSeq libraries ?](https://faqs.lexogen.com/faq/how-long-does-it-take-to-generate-quantseq-librari.md)
* [How long does it take to generate QuantSeq-Pool libraries?](https://faqs.lexogen.com/faq/how-long-does-it-take-to-generate-quantseq-pool-li.md)
* [How long does the generation of full-length double-stranded DNA take?](https://faqs.lexogen.com/faq/how-long-does-the-generation-of-full-length-double.md)
* [How long does the protocol take?](https://faqs.lexogen.com/faq/how-long-does-the-protocol-take.md)
* [How long should the labeling time be?](https://faqs.lexogen.com/faq/how-long-should-the-labeling-time-be.md)
* [How many PCR cycles are needed to amplify QuantSeq libraries?](https://faqs.lexogen.com/faq/how-many-pcr-cycles-are-needed-to-amplify-quantseq.md)
* [How many PCR cycles do I need for brain libraries made using the BC1 Block Module?](https://faqs.lexogen.com/faq/how-many-pcr-cycles-do-i-need-for-brain-libraries-.md)
* [How many PCR cycles do I need to use for blood RNA libraries prepared using Globin Block?](https://faqs.lexogen.com/faq/how-many-pcr-cycles-do-i-need-to-use-for-blood-rna.md)
* [How many PCR cycles should I use to amplify my libraries?](https://faqs.lexogen.com/faq/how-many-pcr-cycles-should-i-use-to-amplify-my-lib.md)
* [How many reads per sample do I need?](https://faqs.lexogen.com/faq/how-many-reads-per-sample-do-i-need.md)
* [How many reads per sample do I need ?](https://faqs.lexogen.com/faq/how-many-reads-per-sample-do-i-need-1.md)
* [How many RNA extractions can be performed with the SPLIT Kit?](https://faqs.lexogen.com/faq/how-many-rna-extractions-can-be-performed-with-the.md)
* [How many runs can be performed with the QuantSeq kit?](https://faqs.lexogen.com/faq/how-many-runs-can-be-performed-with-the-quantseq-k.md)
* [How many samples can I process in a single run?](https://faqs.lexogen.com/faq/how-many-samples-can-i-process-in-a-single-run.md)
* [How many samples can I spike-in with the SIRV mixes?](https://faqs.lexogen.com/faq/how-many-samples-can-i-spike-in-with-the-sirv-mixe.md)
* [How much rRNA is left after depletion with RiboCop HMR V2?](https://faqs.lexogen.com/faq/how-much-rrna-is-left-after-depletion-with-ribocop.md)
* [How much sequencing depth is saved when depleting globin mRNA?](https://faqs.lexogen.com/faq/how-much-sequencing-depth-is-saved-when-depleting-.md)
* [How should I acknowledge Lexogen NGS Services in my publications?](https://faqs.lexogen.com/faq/how-should-i-acknowledge-lexogen-ngs-services-in-m.md)
* [How can I analyze my CORALL V2  Data?](https://faqs.lexogen.com/faq/how-should-i-analyze-corall-v2-sequencing-data.md)
* [How should I analyze TeloPrime IsoSeq data?](https://faqs.lexogen.com/faq/how-should-i-analyze-teloprime-isoseq-data.md)
* [How should I QC my final RNA?](https://faqs.lexogen.com/faq/how-should-i-qc-my-final-rna.md)
* [How should I remove contaminating gDNA from my samples before library prep?](https://faqs.lexogen.com/faq/how-should-i-remove-contaminating-gdna-from-my-sam.md)
* [How should I sequence CORALL V2 libraries? What sequencing format should be used?](https://faqs.lexogen.com/faq/how-should-i-sequence-corall-v2-libraries-what-seq.md)
* [How should I spike-in SIRVs for large experiments (e.g., QuantSeq-Pool)?](https://faqs.lexogen.com/faq/how-should-i-spike-in-sirvs-for-large-experiments-.md)
* [How should my FFPE samples be stored before extraction?](https://faqs.lexogen.com/faq/how-should-my-ffpe-samples-be-stored-before-extrac.md)
* [How should my samples be delivered - tubes/plates, shipping conditions?](https://faqs.lexogen.com/faq/how-should-my-samples-be-delivered-tubes-plates-sh.md)
* [How to use SIRVs](https://faqs.lexogen.com/faq/how-to-use-sirvs.md)
* [How will my data be delivered?](https://faqs.lexogen.com/faq/how-will-my-data-be-delivered.md)
* [I am worried about data security. How are you handling data security at Lexogen?](https://faqs.lexogen.com/faq/i-am-worried-about-data-security-how-are-you-handl.md)
* [I am worried about my samples being lost or damaged during shipment?](https://faqs.lexogen.com/faq/i-am-worried-about-my-samples-being-lost-or-damage.md)
* [I can only extract a limited amount of RNA from my starting material. How much RNA should I send for library preparation?](https://faqs.lexogen.com/faq/i-can-only-extract-a-limited-amount-of-rna-from-my.md)
* [I do not have enough EB in the kit when running an automated protocol. Why is this and what shall I do?](https://faqs.lexogen.com/faq/i-do-not-have-enough-eb-in-the-kit-when-running-on.md)
* [I left my kit, or individual kit components at room temperature, are my products stable?](https://faqs.lexogen.com/faq/i-left-my-kit-or-individual-kit-components-at-room.md)
* [I see internal priming in my QuantSeq data. How can I prevent this?](https://faqs.lexogen.com/faq/i-see-internal-priming-in-my-quantseq-data-how-can.md)
* [I see poly(T) stretches in my QuantSeq REV data and low sequencing quality. What is the reason for this?](https://faqs.lexogen.com/faq/i-see-poly-t-stretches-in-my-quantseq-rev-data-and.md)
* [I want to gel purify my samples. Do you have any recommendations?](https://faqs.lexogen.com/faq/i-want-to-gel-purify-my-samples-do-you-have-any-re.md)
* [I want to ship RNA for a Services project with Lexogen - which quality criteria should my samples meet?](https://faqs.lexogen.com/faq/i-want-to-ship-rna-for-a-services-project-with-lex.md)
* [I would prefer 8 or 10 nt UDIs instead. Is this possible?](https://faqs.lexogen.com/faq/i-would-prefer-8-or-10-nt-udis-instead-is-this-pos.md)
* [Illumina Loading Guidelines for Lexogen libraries](https://faqs.lexogen.com/faq/illumina-loading-guidelines-for-lexogen-libraries.md)
* [In which organisms has TraPR been tested?](https://faqs.lexogen.com/faq/in-which-organisms-has-trapr-been-tested.md)
* [12 nt Unique Dual Indexing](https://faqs.lexogen.com/faq/indexing-solutions.md)
* [Is any manual intervention required during the run?](https://faqs.lexogen.com/faq/is-any-manual-intervention-required-during-the-run.md)
* [Is CORALL mRNA-Seq V2 suitable for use with degraded or FFPE RNA samples?](https://faqs.lexogen.com/faq/is-corall-mrna-seq-v2-suitable-for-use-with-degrad.md)
* [Is CORALL Total RNA-Seq V2 suitable for use with degraded or FFPE RNA samples?](https://faqs.lexogen.com/faq/is-corall-total-rna-seq-v2-suitable-for-use-with-d.md)
* [Is it okay to store kit components upside-down for longer?](https://faqs.lexogen.com/faq/is-it-okay-to-store-kit-components-upside-down-for.md)
* [Is it possible to automate QuantSeq-Pool on a liquid handler?](https://faqs.lexogen.com/faq/is-it-possible-to-automate-quantseq-pool-on-a-liqu.md)
* [Is LUTHOR HD Pool suitable for degraded or FFPE samples?](https://faqs.lexogen.com/faq/is-luthor-hd-pool-suitable-for-degraded-or-ffpe-sa.md)
* [Is miRVEL Discovery Small RNA-Seq Library Prep Kit compatible with heparinized plasma samples?](https://faqs.lexogen.com/faq/is-mirvel-discovery-small-rna-seq-library-prep-kit.md)
* [Is QuantSeq REV V2 suitable for the analysis of FFPE samples?](https://faqs.lexogen.com/faq/is-quantseq-rev-v2-suitable-for-the-analysis-of-ff.md)
* [Is QuantSeq suitable for preparation of libraries from degraded RNA or FFPE samples?](https://faqs.lexogen.com/faq/is-quantseq-suitable-for-preparation-of-libraries-.md)
* [Is QuantSeq with UDI V2 suitable for the analysis of FFPE samples?](https://faqs.lexogen.com/faq/is-quantseq-with-udi-v2-suitable-for-the-analysis-.md)
* [Is RNA/DNA Defender compatible with Lexogen products?](https://faqs.lexogen.com/faq/is-rna-dna-defender-compatible-with-lexogen-produc.md)
* [Is separating Pre-PCR and Post-PCR working areas necessary?](https://faqs.lexogen.com/faq/is-separating-pre-pcr-and-post-pcr-working-areas-n.md)
* [Is TeloPrime compatible with QuantSeq 3’, CORALL or LUTHOR HD Library Prep Kits?](https://faqs.lexogen.com/faq/is-teloprime-compatible-with-quantseq-3-or-corall-.md)
* [Is the data analysis on Kangooroo free of charge?](https://faqs.lexogen.com/faq/is-the-kangooroo-data-analysis-free-of-charge.md)
* [Is the kit suitable for preparation of libraries from degraded RNA or FFPE samples?](https://faqs.lexogen.com/faq/is-the-kit-suitable-for-preparation-of-libraries-f.md)
* [Is the RNA extracted with the SPLIT Kit only appropriate for RNA-Seq?](https://faqs.lexogen.com/faq/is-the-rna-extracted-with-the-split-kit-only-appro.md)
* [Is there a separate automation protocol for QuantSeq REV library preps or for libraries prepared with Globin or BC1 Block and/or UMIs?](https://faqs.lexogen.com/faq/is-there-a-separate-automation-protocol-for-quants.md)
* [Is there a size limit for FASTQ files upload? What should I do if my FASTQ files exceed the size limit?](https://faqs.lexogen.com/faq/is-there-a-size-limit-for-fastq-files-upload--what.md)
* [Is there an index balance checker tool for 12 nt UDIs?](https://faqs.lexogen.com/faq/is-there-an-index-balance-checker-tool-for-12-nt-u.md)
* [Is TraPR-isolated sRNA suitable for high-throughput sequencing?](https://faqs.lexogen.com/faq/is-trapr-isolated-srna-suitable-for-high-throughpu.md)
* [Isoforms that belong to the same gene get the same fragment count. Is that a normal behavior?](https://faqs.lexogen.com/faq/isoforms-that-belong-to-the-same-gene-get-the-same.md)
* [Kangooroo Data Analysis](https://faqs.lexogen.com/faq/kangooroo-data-analysis.md)
* [Kangooroo General](https://faqs.lexogen.com/faq/kangooroo-faqs.md)
* [Kangooroo User Guide](https://faqs.lexogen.com/faq/kangooroo-user-guide.md)
* [Lexogen NGS Services](https://faqs.lexogen.com/faq/lexogen-ngs-services.md)
* [LUTHOR HD](https://faqs.lexogen.com/faq/luthor-3-mrna-seq-library-prep-kits.md)
* [LUTHOR HD Pool](https://faqs.lexogen.com/faq/luthor-hd-pool.md)
* [LUTHOR High Definition](https://faqs.lexogen.com/faq/luthor-high-definition.md)
* [miRVEL Discovery Small RNA-Seq Library Prep](https://faqs.lexogen.com/faq/mirvel-discovery-small-rna-seq-library-prep.md)
* [miRVEL General](https://faqs.lexogen.com/faq/mirvel-general.md)
* [miRVEL Profiling Small RNA-Seq Library Prep](https://faqs.lexogen.com/faq/mirvel-profiling-small-rna-seq-library-prep-kit.md)
* [miRVEL small RNA Analysis](https://faqs.lexogen.com/faq/mirvel-small-rna-analysis.md)
* [miRVEL](https://faqs.lexogen.com/faq/mirvel-small-rna-seq.md)
* [Mix² RNA-Seq Data Analysis Software](https://faqs.lexogen.com/faq/mix2-rna-seq-data-analysis-software.md)
* [Modified protocol for multiple rounds of PolyA selection](https://faqs.lexogen.com/faq/modified-protocol-for-multiple-rounds-of-polya-sel.md)
* [Modules and Add-on Kits](https://faqs.lexogen.com/faq/modules-and-add-on-kits.md)
* [My RNA is heavily degraded. Can it be used for library preparation?](https://faqs.lexogen.com/faq/my-rna-is-heavily-degraded-can-it-be-used-for-libr.md)
* [On which liquid handler is the QuantSeq protocol automated?](https://faqs.lexogen.com/faq/on-which-liquid-handler-is-the-quantseq-protocol-a.md)
* [Our Services offerings](https://faqs.lexogen.com/faq/our-services-offerings.md)
* [PCR Add-on and Reamplification Kit V2](https://faqs.lexogen.com/faq/pcr-add-on-and-reamplification-kit-v2.md)
* [Poly(A) Selection](https://faqs.lexogen.com/faq/poly-a-rna-selection-kit.md)
* [Protocol for Whole Blood mRNA-Seq with Globin Depletion](https://faqs.lexogen.com/faq/protocol-for-whole-blood-mrna-seq-with-globin-depl.md)
* [Purification Module](https://faqs.lexogen.com/faq/purification-module.md)
* [QuantSeq](https://faqs.lexogen.com/faq/quantseq-3-mrna-seq-library-prep-kits.md)
* [QuantSeq and LUTHOR Analysis](https://faqs.lexogen.com/faq/quantseq-and-luthor-analysis.md)
* [QuantSeq Automation](https://faqs.lexogen.com/faq/quantseq-automation.md)
* [QuantSeq FFPE](https://faqs.lexogen.com/faq/quantseq-ffpe.md)
* [QuantSeq-Flex](https://faqs.lexogen.com/faq/quantseq-flex.md)
* [QuantSeq General](https://faqs.lexogen.com/faq/quantseq-general.md)
* [QuantSeq-Pool](https://faqs.lexogen.com/faq/quantseq-pool.md)
* [QuantSeq REV V2](https://faqs.lexogen.com/faq/quantseq-rev-v2.md)
* [QuantSeq UMI Module](https://faqs.lexogen.com/faq/quantseq-umi-module.md)
* [QuantSeq FWD V2](https://faqs.lexogen.com/faq/quantseq-with-udi-v2.md)
* [RiboCop for Bacteria](https://faqs.lexogen.com/faq/ribocop-for-bacteria.md)
* [RiboCop for Fish](https://faqs.lexogen.com/faq/ribocop-for-fish.md)
* [RiboCop for Plant](https://faqs.lexogen.com/faq/ribocop-for-plant.md)
* [RiboCop for Yeast](https://faqs.lexogen.com/faq/ribocop-for-yeast.md)
* [RiboCop General](https://faqs.lexogen.com/faq/ribocop-general.md)
* [RiboCop HMR + Globin](https://faqs.lexogen.com/faq/ribocop-hmr-globin.md)
* [RiboCop Human/Mouse/Rat (HMR) V2](https://faqs.lexogen.com/faq/ribocop-human-mouse-rat-hmr.md)
* [RiboCop](https://faqs.lexogen.com/faq/ribocop-rrna-depletion-kits.md)
* [RNA/DNA Defender](https://faqs.lexogen.com/faq/rna-dna-defender-solution.md)
* [Should I deplete ribosomal RNA using RiboCop before preparing libraries with the Small RNA-Seq Library Prep?](https://faqs.lexogen.com/faq/should-i-deplete-ribosomal-rna-using-ribocop-befor.md)
* [Should I perform a DNase treatment before QuantSeq FFPE?](https://faqs.lexogen.com/faq/should-i-perform-a-dnase-treatment-before-quantseq.md)
* [Should I perform size selection of TeloPrime V2 cDNA for Iso-Seq™?](https://faqs.lexogen.com/faq/should-i-perform-size-selection-of-teloprime-v2-cd.md)
* [Should I treat my SLAMseq RNA samples with DNase I and should this be done before or after alkylation with iodoacetamide?](https://faqs.lexogen.com/faq/should-i-treat-my-slamseq-rna-samples-with-dnase-i.md)
* [SIRV-Sets and Design](https://faqs.lexogen.com/faq/sirv-sets-and-design.md)
* [SIRVs General](https://faqs.lexogen.com/faq/sirvs-general.md)
* [SLAMseq](https://faqs.lexogen.com/faq/slamseq-metabolic-rna-labeling-kits.md)
* [Small RNA-Seq Library Prep Kit](https://faqs.lexogen.com/faq/small-rna-seq-library-prep-kit.md)
* [SIRVs](https://faqs.lexogen.com/faq/spike-in-rna-variant-controls-sirvs.md)
* [SPLIT One-step FFPE RNA Extraction Kit](https://faqs.lexogen.com/faq/split-one-step-ffpe-rna-extraction-kit.md)
* [SPLIT RNA Extraction Kit - General](https://faqs.lexogen.com/faq/split-rna-extraction-kit-general.md)
* [SPLIT](https://faqs.lexogen.com/faq/split-rna-extraction-kits.md)
* [TeloPrime](https://faqs.lexogen.com/faq/teloprime-full-length-cdna-amplification-kit.md)
* [The color of the FFPE Protease solution varies between kits. Is this okay?](https://faqs.lexogen.com/faq/the-color-of-the-ffpe-protease-solution-varies-bet.md)
* [The yield of my library is low, what can I do?](https://faqs.lexogen.com/faq/the-yield-of-my-library-is-low-what-can-i-do.md)
* [TraPR](https://faqs.lexogen.com/faq/trapr-small-rna-isolation-kit.md)
* [What are the adapter sequences for miRVEL Discovery?](https://faqs.lexogen.com/faq/what-are-the-adapter-sequences.md)
* [What are the adapter sequences for miRVEL Profiling?](https://faqs.lexogen.com/faq/what-are-the-adapter-sequences-for-mirvel-profilin.md)
* [What are the adapter sequences for trimming?](https://faqs.lexogen.com/faq/what-are-the-adapter-sequences-for-trimming-.md)
* [What are the concentrations of the SIRVs?](https://faqs.lexogen.com/faq/what-are-the-concentrations-of-the-sirvs.md)
* [What are the critical steps in the LUTHOR HD 3’ mRNA-Seq protocol?](https://faqs.lexogen.com/faq/what-are-the-critical-steps-in-the-luthor-hd-3-mrn.md)
* [What are the differences between CORALL Total V2 and CORALL FFPE? Are the results comparable?](https://faqs.lexogen.com/faq/what-are-the-differences-between-corall-total-v2-a.md)
* [What are the differences between LUTHOR HD and LUTHOR HD Pool? Are any of the components interchangeable between kits?](https://faqs.lexogen.com/faq/what-are-the-differences-between-luthor-hd-and-lut.md)
* [What are the differences between QS FFPE and QuantSeq V2 kits?](https://faqs.lexogen.com/faq/what-are-the-differences-between-qs-ffpe-and-quant.md)
* [What are the differences between QuantSeq REV and FWD?](https://faqs.lexogen.com/faq/what-are-the-differences-between-quantseq-rev-and-.md)
* [What are the input requirements?](https://faqs.lexogen.com/faq/what-are-the-input-requirements.md)
* [What are the input requirements for QuantSeq FFPE?](https://faqs.lexogen.com/faq/what-are-the-input-requirements-for-quantseq-ffpe.md)
* [What are the input RNA requirements?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements.md)
* [What are the input RNA requirements for miRVEL Discovery?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements-1.md)
* [What are the input RNA requirements for miRVEL Profiling ?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements-for-mirvel-pro.md)
* [What are the input RNA requirements for QuantSeq FWD?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements-for-quantseq-f.md)
* [What are the input RNA requirements for QuantSeq REV?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements-for-quantseq-r.md)
* [What are the input RNA requirements for TeloPrime?](https://faqs.lexogen.com/faq/what-are-the-input-rna-requirements-for-teloprime.md)
* [What are the key considerations when using this kit?](https://faqs.lexogen.com/faq/what-are-the-key-considerations-when-using-this-ki.md)
* [What are the minimum and maximum input amounts for SPLIT?](https://faqs.lexogen.com/faq/what-are-the-minimum-and-maximum-input-amounts-for.md)
* [What are the minimum and maximum number of samples I can pool into a single tube?](https://faqs.lexogen.com/faq/what-are-the-minimum-and-maximum-number-of-samples.md)
* [What are the most critical steps in the QuantSeq library generation ?](https://faqs.lexogen.com/faq/what-are-the-most-critical-steps-in-the-quantseq-l.md)
* [What are the Plate Adapters and when should I use them?](https://faqs.lexogen.com/faq/what-are-the-plate-adapters-and-when-should-i-use-.md)
* [What are the properties of the SIRV transcripts’ terminal sequences?](https://faqs.lexogen.com/faq/what-are-the-properties-of-the-sirv-transcripts-te.md)
* [What are the RNA input requirements for LUTHOR HD 3’ mRNA-Seq?](https://faqs.lexogen.com/faq/what-are-the-rna-input-requirements-for-luthor-hd-.md)
* [What are the updates to QuantSeq REV V2?](https://faqs.lexogen.com/faq/what-are-the-updates-to-quantseq-rev-v2.md)
* [What are Unique Molecular Identifiers (UMIs)?](https://faqs.lexogen.com/faq/what-are-unique-molecular-identifiers-umis.md)
* [What bioinformatics data analysis services are you offering?](https://faqs.lexogen.com/faq/what-bioinformatics-data-analysis-services-are-you.md)
* [What can I do if my libraries are undercycled ?](https://faqs.lexogen.com/faq/what-can-i-do-if-my-libraries-are-undercycled.md)
* [What can I do if my QuantSeq REV V2 libraries are undercycled?](https://faqs.lexogen.com/faq/what-can-i-do-if-my-quantseq-rev-v2-libraries-are-.md)
* [What can I do if my QuantSeq with UDI V2 libraries are undercycled?](https://faqs.lexogen.com/faq/what-can-i-do-if-my-quantseq-with-udi-v2-libraries.md)
* [What changed between QuantSeq with UDI V1 and V2?](https://faqs.lexogen.com/faq/what-changed-between-quantseq-with-udi-v1-and-v2.md)
* [What changed between the UDI Add-on kits V1 and V2?](https://faqs.lexogen.com/faq/what-changed-between-the-udi-add-on-kits-v1-and-v2.md)
* [What concentration of targeted primers should I use?](https://faqs.lexogen.com/faq/what-concentration-of-targeted-primers-should-i-us.md)
* [What cycle number do I need to use to amplify my targeted sequencing library?](https://faqs.lexogen.com/faq/what-cycle-number-do-i-need-to-use-to-amplify-my-t.md)
* [What data analysis pipelines are available on Kangooroo?](https://faqs.lexogen.com/faq/what-data-analysis-pipelines-are-available.md)
* [What deliverables are being sent after the data analysis?](https://faqs.lexogen.com/faq/what-deliverables-are-being-sent-after-the-data-an.md)
* [What do I do if my products arrive thawed or damaged?](https://faqs.lexogen.com/faq/what-do-i-do-if-my-products-arrive-thawed-or-damag.md)
* [What do I need for the qPCR Assay?](https://faqs.lexogen.com/faq/what-do-i-need-for-the-qpcr-assay.md)
* [What do I need for the reamplification PCR?](https://faqs.lexogen.com/faq/what-do-i-need-for-the-reamplification-pcr.md)
* [What do Kangooroo pipelines offer?](https://faqs.lexogen.com/faq/what-do-kangooroo-pipelines-offer-.md)
* [What does a typical data report look like?](https://faqs.lexogen.com/faq/what-does-a-typical-data-report-look-like.md)
* [What does a typical library trace of miRVEL Discovery Small RNA-Seq Library look like?](https://faqs.lexogen.com/faq/what-does-a-typical-library-trace-of-mirvel-discov.md)
* [What does a typical library trace of miRVEL Profiling Small RNA-Seq Library look like?](https://faqs.lexogen.com/faq/what-does-a-typical-library-trace-of-mirvel-profil.md)
* [What does a typical LUTHOR HD 3’ mRNA-Seq library look like?](https://faqs.lexogen.com/faq/what-does-a-typical-luthor-hd-3-mrna-seq-library-l.md)
* [What does a typical LUTHOR HD Pool library look like?](https://faqs.lexogen.com/faq/what-does-a-typical-luthor-hd-pool-library-look-li.md)
* [What does hamming distance mean? What is the hamming distance of Lexogen’s i5 and i7 indices?](https://faqs.lexogen.com/faq/what-does-hamming-distance-mean-what-is-the-hammin.md)
* [What does my voucher code include?](https://faqs.lexogen.com/faq/what-does-my-voucher-code-include.md)
* [What does this peak above the upper marker of my library trace mean?](https://faqs.lexogen.com/faq/what-does-this-peak-above-the-upper-marker-of-my-l.md)
* [What downstream applications can the full-length cDNA be used for?](https://faqs.lexogen.com/faq/what-downstream-applications-can-the-full-length-c.md)
* [What effect does Mycoplasma have on QuantSeq data analysis?](https://faqs.lexogen.com/faq/what-effect-does-mycoplasma-have-on-quantseq-data-.md)
* [What factors should I consider when switching from QuantSeq-FWD to QuantSeq-Pool?](https://faqs.lexogen.com/faq/what-factors-should-i-consider-when-switching-from.md)
* [What happens if my samples fail quality control (QC)?](https://faqs.lexogen.com/faq/what-happens-if-my-samples-fail-quality-control-qc.md)
* [What input amount of total RNA is needed for the alkylation with iodoacetamide?](https://faqs.lexogen.com/faq/what-input-amount-of-total-rna-is-needed-for-the-a.md)
* [What input amounts of fish RNA can be used?](https://faqs.lexogen.com/faq/what-input-amounts-of-fish-rna-can-be-used.md)
* [What input amounts of plant RNA can be used?](https://faqs.lexogen.com/faq/what-input-amounts-of-plant-rna-can-be-used.md)
* [What input amounts of RNA can be used?](https://faqs.lexogen.com/faq/what-input-amounts-of-rna-can-be-used.md)
* [What input amounts of yeast RNA can be used?](https://faqs.lexogen.com/faq/what-input-amounts-of-yeast-rna-can-be-used.md)
* [What input amounts should I use?](https://faqs.lexogen.com/faq/what-input-amounts-should-i-use.md)
* [What is included in my differential gene expression analysis?](https://faqs.lexogen.com/faq/what-is-included-in-my-differential-gene-expressio.md)
* [What is the adapter sequence needed for Read 1 trimming?](https://faqs.lexogen.com/faq/what-is-the-adapter-sequence-i-need-to-use-for-t-2.md)
* [What is the CSP and how do I use it?](https://faqs.lexogen.com/faq/what-is-the-csp-and-how-do-i-use-it.md)
* [What is the difference between LUTHOR HD 3' mRNA-Seq and QuantSeq 3’ mRNA-Seq?](https://faqs.lexogen.com/faq/what-is-the-difference-between-luthor-hd-3-mrna-se.md)
* [What is the difference between QuantSeq FWD and QuantSeq REV protocols?](https://faqs.lexogen.com/faq/what-is-the-difference-between-quantseq-fwd-and-qu.md)
* [What is the difference between QuantSeq-Pool and QuantSeq FWD?](https://faqs.lexogen.com/faq/what-is-the-difference-between-quantseq-pool-and-s.md)
* [What is the difference between the ERCCs and the SIRVs?](https://faqs.lexogen.com/faq/what-is-the-difference-between-the-erccs-and-the-s.md)
* [What is the difference between the PCR Add-on Kit  and the PCR Add-on and Reamplification Kit V2?](https://faqs.lexogen.com/faq/what-is-the-difference-between-the-pcr-add-on-kit-.md)
* [What is the effect of gDNA contamination on my data?](https://faqs.lexogen.com/faq/what-is-the-effect-of-gdna-contamination-on-my-dat.md)
* [What is the expected RNA recovery rate after rRNA depletion?](https://faqs.lexogen.com/faq/what-is-the-expected-rna-recovery-rate-after-rrna-.md)
* [What is the expected yield? Why is my yield low?](https://faqs.lexogen.com/faq/what-is-the-expected-yield-why-is-my-yield-low.md)
* [What is the length of the oligo(dT)?](https://faqs.lexogen.com/faq/what-is-the-length-of-the-oligo-dt.md)
* [What is the optimal sequencing read length for Small RNA-Seq libraries?](https://faqs.lexogen.com/faq/what-is-the-optimal-sequencing-read-length-for-sma.md)
* [What is the orientation of QuantSeq FWD reads ?](https://faqs.lexogen.com/faq/what-is-the-orientation-of-quantseq-fwd-reads.md)
* [What is the orientation of QuantSeq REV reads?](https://faqs.lexogen.com/faq/what-is-the-orientation-of-quantseq-rev-reads.md)
* [What is the output?](https://faqs.lexogen.com/faq/what-is-the-output.md)
* [What is the poly(A) RNA recovery?](https://faqs.lexogen.com/faq/what-is-the-poly-a-rna-recovery.md)
* [What is the prominent peak around 350bp in my RTL CORALL V2 libraries generated from rRNA-depleted input RNA?](https://faqs.lexogen.com/faq/what-is-the-prominent-peak-around-350bp-in-my-rtl-.md)
* [What is the recommended input for CORALL mRNA-Seq V2 library preparation?](https://faqs.lexogen.com/faq/what-is-the-recommended-input-for-corall-mrna-seq-.md)
* [What is the recommended input for CORALL Total RNA-Seq V2 library preparation?](https://faqs.lexogen.com/faq/what-is-the-recommended-input-for-corall-total-rna.md)
* [What is the recommended input for LUTHOR HD Pool library preparation?](https://faqs.lexogen.com/faq/what-is-the-recommended-input-for-luthor-hd-pool-l.md)
* [What is the recommended sequencing depth for SLAMseq-QuantSeq experiments?](https://faqs.lexogen.com/faq/what-is-the-recommended-sequencing-depth-for-slams.md)
* [What is the recommended sequencing format and read depth?](https://faqs.lexogen.com/faq/what-is-the-recommended-sequencing-format-and-read.md)
* [What is the recommended sequencing format for SLAMseq-QuantSeq experiments?](https://faqs.lexogen.com/faq/what-is-the-recommended-sequencing-format-for-slam.md)
* [What is the shortest labeling duration recommended before beginning time course sampling?](https://faqs.lexogen.com/faq/what-is-the-shortest-labeling-duration-recommended.md)
* [What is the typical fragment size for QuantSeq Libraries?](https://faqs.lexogen.com/faq/what-is-the-typical-fragment-size-for-quantseq-lib.md)
* [What is the typical library size distribution for QuantSeq FFPE libraries?](https://faqs.lexogen.com/faq/what-is-the-typical-library-size-distribution-fo-1.md)
* [What is the typical library size distribution for CORALL FFPE libraries?](https://faqs.lexogen.com/faq/what-is-the-typical-library-size-distribution-fo-2.md)
* [What is the typical library size distribution for QuantSeq-Pool?](https://faqs.lexogen.com/faq/what-is-the-typical-library-size-distribution-for-.md)
* [What is the typical RNA yield?](https://faqs.lexogen.com/faq/what-is-the-typical-rna-yield.md)
* [What is the typical yield I should get from my library prep?](https://faqs.lexogen.com/faq/what-is-the-typical-yield-i-should-get-from-my-lib.md)
* [What is your turnaround time?](https://faqs.lexogen.com/faq/what-is-your-turnaround-time.md)
* [What kit is the BC1 Block Module compatible with?](https://faqs.lexogen.com/faq/what-kit-is-the-bc1-block-module-compatible-with.md)
* [What level of depletion can be expected from RiboCop for Yeast?](https://faqs.lexogen.com/faq/what-level-of-depletion-can-be-expected-from-rib-1.md)
* [What level of depletion can be expected from RiboCop for Plants?](https://faqs.lexogen.com/faq/what-level-of-depletion-can-be-expected-from-rib-2.md)
* [What level of depletion can be expected from RiboCop for Fish?](https://faqs.lexogen.com/faq/what-level-of-depletion-can-be-expected-from-rib-3.md)
* [What level of depletion can be expected from RiboCop for Bacteria?](https://faqs.lexogen.com/faq/what-level-of-depletion-can-be-expected-from-riboc.md)
* [What level of globin depletion does RiboCop HMR+Globin achieve?](https://faqs.lexogen.com/faq/what-level-of-depletion-does-ribocop-hmr-globin-ac.md)
* [What level of multiplexing can be provided with QuantSeq?  What barcoding (indexing) system do you use?](https://faqs.lexogen.com/faq/what-level-of-multiplexing-can-be-provided-with-qu.md)
* [What loading amount should I use for sequencing CORALL V2 libraries?](https://faqs.lexogen.com/faq/what-loading-amount-should-i-use-for-sequencing-co.md)
* [What multiplexing options are available for QuantSeq-Pool?](https://faqs.lexogen.com/faq/what-multiplexing-options-are-available-for-quants.md)
* [What output files do I get for CORALL data analysis with Kangooroo?](https://faqs.lexogen.com/faq/what-output-files-do-i-get-for-corall-data-analysi.md)
* [What output files do I get for miRVEL data analysis with Kangooroo?](https://faqs.lexogen.com/faq/what-output-files-do-i-get-for-mirvel-data-analysi.md)
* [What output files do I get for WTS data analysis with Kangooroo?](https://faqs.lexogen.com/faq/what-output-files-do-i-get-for-wts-data-analysis-w.md)
* [What output files do I get for QuantSeq and LUTHOR HD data analysis with Kangooroo?](https://faqs.lexogen.com/faq/what-output-files-do-i-get-with-kangooroo.md)
* [What positive control do you recommend to use ?](https://faqs.lexogen.com/faq/what-positive-control-do-you-recommend-to-use.md)
* [What read length should I use for QuantSeq-Pool Reads 1 and 2?](https://faqs.lexogen.com/faq/what-read-length-should-i-use-for-quantseq-pool-re.md)
* [What read lengths should I use for LUTHOR HD Reads 1 and 2?](https://faqs.lexogen.com/faq/what-read-lengths-should-i-use-for-luthor-hd-reads.md)
* [What recommendations do you have for targeting rare, or low-abundance transcripts?](https://faqs.lexogen.com/faq/what-recommendations-do-you-have-for-targeting-rar.md)
* [What RNA input amounts can be used?](https://faqs.lexogen.com/faq/what-rna-input-amounts-can-be-used.md)
* [What RNA species does TraPR isolate?](https://faqs.lexogen.com/faq/what-rna-species-does-trapr-isolate.md)
* [What RNAs are recovered after extraction?](https://faqs.lexogen.com/faq/what-rnas-are-recovered-after-extraction.md)
* [What rRNA subtypes does RiboCop for Fish target?](https://faqs.lexogen.com/faq/what-rrna-subtypes-does-ribocop-for-fish-target.md)
* [What rRNA subtypes does RiboCop for Plants target?](https://faqs.lexogen.com/faq/what-rrna-subtypes-does-ribocop-for-plants-target.md)
* [What sample types has RiboCop for Fish been tested on?](https://faqs.lexogen.com/faq/what-sample-types-has-ribocop-for-fish-been-tested.md)
* [What sample types has RiboCop for Plants been tested on?](https://faqs.lexogen.com/faq/what-sample-types-has-ribocop-for-plants-been-test.md)
* [What sample types has RiboCop HMR + Globin been tested on?](https://faqs.lexogen.com/faq/what-sample-types-has-ribocop-hmr-globin-been-test.md)
* [What sequences should be trimmed ?](https://faqs.lexogen.com/faq/what-sequences-should-be-trimmed.md)
* [What sequences should be trimmed?](https://faqs.lexogen.com/faq/what-sequences-should-be-trimmed-1.md)
* [What sequencing platforms is Lexogen using for RNA-Seq?](https://faqs.lexogen.com/faq/what-sequencing-platforms-is-lexogen-using-for-rna.md)
* [What sequencing read length and read depth are recommended for QuantSeq FFPE?](https://faqs.lexogen.com/faq/what-sequencing-read-length-and-read-depth-are-rec.md)
* [What sequencing read length is best suited for QuantSeq REV libraries?](https://faqs.lexogen.com/faq/what-sequencing-read-length-is-best-suited-for-q-1.md)
* [What sequencing read length is best suited for QuantSeq FWD libraries ?](https://faqs.lexogen.com/faq/what-sequencing-read-length-is-best-suited-for-qua.md)
* [What sequencing read length is optimal for Small RNA-Seq libraries?](https://faqs.lexogen.com/faq/what-sequencing-read-length-is-optimal-for-small-r.md)
* [What should be used as a control?](https://faqs.lexogen.com/faq/what-should-be-used-as-a-control.md)
* [Do you have any recommendations for custom primer design?](https://faqs.lexogen.com/faq/what-should-i-take-into-consideration-when-designi.md)
* [What size distribution can I expect from my libraries?](https://faqs.lexogen.com/faq/what-size-distribution-can-i-expect-from-my-librar.md)
* [What size distribution can I expect from my QuantSeq with UDI V2 libraries?](https://faqs.lexogen.com/faq/what-size-distribution-can-i-expect-from-my-quants.md)
* [What solution is the 4-Thiouridine (S4U) dissolved in?](https://faqs.lexogen.com/faq/what-solution-is-the-4-thiouridine-s4u-dissolved-i.md)
* [What species are available for my data analysis?](https://faqs.lexogen.com/faq/what-species-are-available-for-my-data-analysis.md)
* [What species are available for my small RNA data analysis?](https://faqs.lexogen.com/faq/what-species-are-available-for-my-small-rna-data-a.md)
* [What standard NGS service packages are you offering?](https://faqs.lexogen.com/faq/what-standard-ngs-service-packages-are-you-offerin.md)
* [What starting materials are you accepting?](https://faqs.lexogen.com/faq/what-starting-materials-are-you-accepting.md)
* [What temperature should RNA extraction be performed at?](https://faqs.lexogen.com/faq/what-temperature-should-rna-extraction-be-performe.md)
* [What temperature should the purification beads be during the purification steps?](https://faqs.lexogen.com/faq/what-temperature-should-the-purification-beads-be-.md)
* [When are UMIs useful for library preparation?](https://faqs.lexogen.com/faq/when-are-umis-useful-for-library-preparation.md)
* [Which adaptor dilution should be used for small RNA library preparation with TraPR-enriched sRNAs?](https://faqs.lexogen.com/faq/when-using-lexogens-small-rna-seq-library-prep-wit.md)
* [Where can I find the Safety Data Sheet (SDS) for the kit?](https://faqs.lexogen.com/faq/where-can-i-find-the-safety-data-sheet-sds-for-the.md)
* [Where do I find my voucher code for data analysis?](https://faqs.lexogen.com/faq/where-do-i-find-my-activation-code-for-the-include.md)
* [Where do I find the voucher code for free QuantSeq data analysis?](https://faqs.lexogen.com/faq/where-do-i-find-my-code-for-the-included-quantseq-.md)
* [Where do I find the User Guide for my kit?](https://faqs.lexogen.com/faq/where-do-i-find-the-user-guide-for-my-kit.md)
* [Which aligner should be used for QuantSeq FWD data analysis ?](https://faqs.lexogen.com/faq/which-aligner-should-be-used-for-quantseq-fwd-data.md)
* [Which aligners can be used to align the data to be processed with Mix²?](https://faqs.lexogen.com/faq/which-aligners-can-be-used-to-align-the-data-to-be.md)
* [Which Dual Indexing Kits are compatible with QuantSeq?](https://faqs.lexogen.com/faq/which-dual-indexing-kits-are-compatible-with-quant.md)
* [Which kits and modules are compatible with the UMI Second Strand Synthesis Module for QuantSeq FWD?](https://faqs.lexogen.com/faq/which-kits-and-modules-are-compatible-with-the-umi.md)
* [Which kits are the Globin Block Modules compatible with?](https://faqs.lexogen.com/faq/which-kits-are-the-globin-block-modules-compatible.md)
* [Which Kits do I need for CORALL RNA-Seq V2 library preparation?](https://faqs.lexogen.com/faq/which-kits-do-i-need-for-corall-rna-seq-v2-library.md)
* [Which library preps are compatible with the WTS data analysis pipeline?](https://faqs.lexogen.com/faq/which-library-preps-are-compatible-with-the-wts-da.md)
* [Which miRVEL library prep kit should I choose?](https://faqs.lexogen.com/faq/which-mirvel-library-prep-kit-should-i-choose-.md)
* [Which NGS library preparation kit can be used after generation of cDNA with TeloPrime?](https://faqs.lexogen.com/faq/which-ngs-library-preparation-kit-can-be-used-afte.md)
* [Which operating systems is Mix² available for?](https://faqs.lexogen.com/faq/which-operating-systems-is-mix2-available-for.md)
* [Which organisms have been successfully used with SPLIT?](https://faqs.lexogen.com/faq/which-organisms-are-compatible-with-split.md)
* [Which protocol should I follow, RTM or RTL? What are the differences and how do I choose?](https://faqs.lexogen.com/faq/which-protocol-should-i-follow-rtm-or-rtl-what-are.md)
* [Which reverse transcriptase should be used to read through alkylated S4U nucleotides?](https://faqs.lexogen.com/faq/which-reverse-transcriptase-should-be-used-to-read.md)
* [Which RNA and library preparation methods can be used with the SIRVs?](https://faqs.lexogen.com/faq/which-rna-and-library-preparation-methods-can-be-u.md)
* [Which RNA types can I expect in the small and large RNA-enriched fractions?](https://faqs.lexogen.com/faq/which-rna-types-can-i-expect-in-the-small-and-larg.md)
* [Which RNAs are isolated using the Poly(A) RNA Selection Kit?](https://faqs.lexogen.com/faq/which-rnas-are-isolated-using-the-poly-a-rna-selec.md)
* [Which sample types are compatible with the miRVEL Small RNA-Seq Library Prep Kits?](https://faqs.lexogen.com/faq/which-sample-types-are-compatible-with-the-mirvel-.md)
* [Which sequences are used for PCR amplification?](https://faqs.lexogen.com/faq/which-sequences-are-used-for-pcr-amplification.md)
* [Which sequences do I need to enter into my sample sheet for demultiplexing with Illumina software tools?](https://faqs.lexogen.com/faq/which-sequences-do-i-need-to-enter-into-my-sample-.md)
* [Which Sequencing Platforms are Lexogen Libraries Compatible with?](https://faqs.lexogen.com/faq/which-sequencing-platforms-are-lexogen-libraries-c.md)
* [Which sequencing platforms are suitable for QuantSeq REV libraries?](https://faqs.lexogen.com/faq/which-sequencing-platforms-are-suitable-for-quan-1.md)
* [Which sequencing platforms are suitable for QuantSeq FWD libraries ?](https://faqs.lexogen.com/faq/which-sequencing-platforms-are-suitable-for-quants.md)
* [Which species are Globin Block Modules available for?](https://faqs.lexogen.com/faq/which-species-are-globin-block-modules-available-f.md)
* [Which species can I use the RiboCop HMR V2 rRNA Depletion Kit with?](https://faqs.lexogen.com/faq/which-species-can-i-use-the-ribocop-hmr-rrna-deple.md)
* [Which species can the BC1 Block Module be used with?](https://faqs.lexogen.com/faq/which-species-can-the-bc1-block-module-be-used-wit.md)
* [Which transcripts are depleted with this module? What is the depletion rate?](https://faqs.lexogen.com/faq/which-transcripts-are-depleted-with-this-module-wh.md)
* [Whole Transcriptome Sequencing Analysis](https://faqs.lexogen.com/faq/whole-transcriptome-sequencing-analysis.md)
* [Why are the SIRV isoforms available as 3 mixes?](https://faqs.lexogen.com/faq/why-are-the-sirv-isoforms-available-as-3-mixes.md)
* [Why do I need to do a qPCR assay for CORALL V2 libraries? How does the qPCR assay work?](https://faqs.lexogen.com/faq/why-do-i-need-to-do-a-qpcr-assay-for-corall-v2-lib.md)
* [Why do I need to perform a qPCR? Can this step be skipped?](https://faqs.lexogen.com/faq/why-do-i-need-to-perform-a-qpcr-can-this-step-be-s.md)
* [Why do I see a high % of Duplicate Sequences (FastQC) in my QuantSeq data?](https://faqs.lexogen.com/faq/why-do-i-see-a-high-of-duplicate-sequences-fastqc-.md)
* [Why do I see a peak at ~ 200 bp in my libraries?](https://faqs.lexogen.com/faq/why-do-i-see-a-peak-at-200-bp-in-my-libraries.md)
* [Why do my RNA traces show distinct peaks after RiboCop for Plants?](https://faqs.lexogen.com/faq/why-do-my-rna-traces-show-distinct-peaks-after-rib.md)
* [Why does Mix² report some genes as skipped?](https://faqs.lexogen.com/faq/why-does-mix2-report-some-genes-as-skipped.md)
* [Why does the product label have a different number to the Catalog Number I ordered?](https://faqs.lexogen.com/faq/why-does-the-product-label-have-a-different-number.md)
* [Why don’t you display prices for your Services?](https://faqs.lexogen.com/faq/why-dont-you-display-prices-for-your-services.md)
* [Why is the percentage of rRNA reads higher when globin is depleted?](https://faqs.lexogen.com/faq/why-is-the-percentage-of-rrna-reads-higher-when-gl.md)
* [Why should I include SIRV spike-ins in my experiment?](https://faqs.lexogen.com/faq/why-should-i-include-sirv-spike-ins-in-my-experime.md)
* [With which species is CORALL V2 compatible?](https://faqs.lexogen.com/faq/with-which-species-is-corall-v2-compatible.md)