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Thread | Thread Starter | Forum | Replies | Last Post |
can we know target region of exome without bed file ? | cjo4m4fm | Bioinformatics | 3 | 10-01-2013 12:19 PM |
On/off target rate for whole exome data | chris | Bioinformatics | 5 | 01-21-2013 01:56 AM |
Is it necessary to trim the low quality ends before analyzing exome seq data? | gary | Bioinformatics | 0 | 10-11-2012 08:00 PM |
BAM2MPG Exome Target File | MolecularToast | Bioinformatics | 0 | 07-17-2012 07:49 AM |
Estimate on-target coverage for exome data | pravee1216 | Bioinformatics | 10 | 04-12-2012 12:20 PM |
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#1 |
Junior Member
Location: Beijing,China Join Date: May 2013
Posts: 6
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Dear all,
I am now analyzing some downloaded WES data to find SNPs and there certainly could have reads map to introns. My questions are: Should I remove these reads map to intons or just keep them? What difference does it make? I plan to use USCS RefSeq Gene as annotation of exon boundaries, are there any notable difference between this annotation and exon array used to purify exome during experiment? Thanks! ![]() |
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