Downstream Analysis of snvs
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21 months ago
Hyper_Odin ▴ 310

Dear all, I have hundreds of vcf files (with SNV, indels) from tumor-normal samples. I am confused about how to perform downstream analysis. Is there any typical workflow or any r /python package?

I am lost! Can somebody point me in a direction.!

Thanks
snv sequencing exome • 553 views
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What hypothesis / question are you trying to answer?

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we are trying to look at different snv's, and indels that could cause sarcoma.

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