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Thread | Thread Starter | Forum | Replies | Last Post |
Minimum short read required for transcriptome assembly | edge | Bioinformatics | 4 | 08-25-2013 10:16 PM |
SNP calling reads number | wanguan2000 | Bioinformatics | 1 | 11-25-2011 09:16 AM |
Coverage required for Sanger based SNP detection and Genotyping | gavin.oliver | De novo discovery | 3 | 08-30-2011 01:41 AM |
Coverage required for SNP detection? | Kasycas | De novo discovery | 3 | 04-12-2011 11:38 PM |
SNP detection | doxologist | Genomic Resequencing | 14 | 09-06-2010 07:49 AM |
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#1 |
Junior Member
Location: Durham, UK Join Date: Aug 2009
Posts: 1
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Hello,
I am just planning my first use of Solexa/Illumina sequencing. I'm hoping to use this to sequence the transcriptome of a non-model small mammal in order to identify SNPs. RNA from several different individuals and tissues would be pooled for sequencing. Can anyone tell me, approximately how many sequencing runs I would need to obtain adequate coverage in order to do this? Thanks very much, Tom |
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#2 |
Junior Member
Location: Santa Clara, CA Join Date: Aug 2009
Posts: 2
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Tom,
No answer here, but I'm in a similar boat and was waiting to see if anyone had an answer to your question. I've got a mustard that is 85-90% similar in nucleotide sequences of coding regions to Arabidopsis thaliana. I think I'll need to assemble de novo, then tBlastx my contigs to the Arabidopsis unigenes. Has anyone tried this for transcriptomes of non-model (but close to model) systems? Justen |
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