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Thread | Thread Starter | Forum | Replies | Last Post |
NextSeq 500, High-Output Paired end reads - upper/lower limits for insert sizes? | husseh01 | Illumina/Solexa | 7 | 04-25-2018 11:52 PM |
Bioanalyzer/TapeStation fragment sizes larger than agarose gel | cpylant | Sample Prep / Library Generation | 2 | 10-30-2017 07:48 AM |
New NextSeq: First run. A few issues. | hoytpr | Illumina/Solexa | 5 | 04-20-2017 12:57 PM |
Variance of fragment sizes | minhduc | Sample Prep / Library Generation | 3 | 05-21-2012 12:42 AM |
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#1 |
Junior Member
Location: Massachusetts Join Date: Jul 2018
Posts: 6
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Hello,
I'm still learning the boundaries of the NextSeq and was wondering if anyone had experience with the following or advice where I could find more information. I am trying to optimize run space on our Illumina NextSeq and combine multiple projects including 275bp amplicons and 400bp metagenomic libraries (bp not including adaptor/barcode lengths) into one HT run. My issue is getting predictable coverage of each project; the competitive binding of smaller fragments usually means I end up with way more coverage of the small amplicons than I originally allocated space to and not enough coverage of the metagenomes. Is there a more accurate method to calculate the division of the run? Thank you |
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Tags |
fragment sizes, illumina, nextseq500/550, run coverage, sequencing |
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