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User Guides
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FAQs
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What sequencing coverage is recommended?
-
What do I do if my sequencing run is overclustered?
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What do I do if my sequencing run is underclustered?
-
What if my pass-filter read is < 85 % after sequencing?
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How do I quantify my Tapestri library for sequencing?
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Can I use NextSeq 500/550 to sequence my libraries?
-
Is the Custom Sequencing Primer required?
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Can I convert BCL files to FASTQ files?
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What causes a low % of mapped reads to cells?
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Can I reduce the DNA library concentration to < 5 nM?
-
How many samples can I pool with the sample indices?
-
Are undetermined FASTQ files required for Pipeline?
-
Which sequencing chemistry do you recommend?
-
What loading concentration should I use?
-
Which sequencer should I use?
-
What concentration of PhiX should I use?
-
Can I pool Tapestri and other libraries on my sequencer?
-
Can I use PE 250 bp sequencing chemistry to improve FLT3-ITD detection?
-
What sequencing coverage is recommended?
-
User Guides
-
FAQs
-
What sequencing coverage is recommended?
-
What do I do if my sequencing run is overclustered?
-
What do I do if my sequencing run is underclustered?
-
What if my pass-filter read is < 85 % after sequencing?
-
How do I quantify my Tapestri library for sequencing?
-
Can I use NextSeq 500/550 to sequence my libraries?
-
Is the Custom Sequencing Primer required?
-
Can I convert BCL files to FASTQ files?
-
What causes a low % of mapped reads to cells?
-
Can I reduce the DNA library concentration to < 5 nM?
-
How many samples can I pool with the sample indices?
-
Are undetermined FASTQ files required for Pipeline?
-
Which sequencing chemistry do you recommend?
-
What loading concentration should I use?
-
Which sequencer should I use?
-
What concentration of PhiX should I use?
-
Can I pool Tapestri and other libraries on my sequencer?
-
Can I use PE 250 bp sequencing chemistry to improve FLT3-ITD detection?
-
What sequencing coverage is recommended?