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#1 |
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Location: Connecticut Join Date: Jun 2009
Posts: 74
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Hi,
This may have been discussed before but I couldn't find the right info. I am trying to identify somatic lesions in tumor DNA. For point mutations, I use ucsc snp131 single base entries to screen out common polymorphisms. For indels, however, ucsc snp131 entries are not positioned to left most base location. As a result, my dindel/samtools output cannot be directly compared with the ucsc snp131 indel entries. Does anyone know where such left-most positioned indel database can be found? Thanks in advance, CSoong PS: I also have germline sequencing data coming along, but for now I was hoping to do some prelim analysis with know indel polymorphism in the population. |
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