Hi all,
I performed whole exome sequencing with 2x 100bp paired end sequencing on the Illumina Genome Analyzer II. I aligned the reads with BWA and then tried to find indels using both VarScan and Dindel version 1.01. For the dindel programme, I just followed the manual.
However, when I look at the indels found with Dindel, 86% of the indels that are found, are 1 basepair indels. (When I used VarScan, 69% of the found indels are 1 basepair.) This seems a lot to me. Could this be because of the presence of nearby SNPs? Does anybody has experiences with this?
Also, the largest indels I've found are 4 basepairs. However, I thought that dindel could find much longer indels?
Thanks a lot,
Lien
I performed whole exome sequencing with 2x 100bp paired end sequencing on the Illumina Genome Analyzer II. I aligned the reads with BWA and then tried to find indels using both VarScan and Dindel version 1.01. For the dindel programme, I just followed the manual.
However, when I look at the indels found with Dindel, 86% of the indels that are found, are 1 basepair indels. (When I used VarScan, 69% of the found indels are 1 basepair.) This seems a lot to me. Could this be because of the presence of nearby SNPs? Does anybody has experiences with this?
Also, the largest indels I've found are 4 basepairs. However, I thought that dindel could find much longer indels?
Thanks a lot,
Lien
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