Downstream Analysis of snvs
0
0
Entering edit mode
2.4 years ago
Hyper_Odin ▴ 320

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 • 682 views
ADD COMMENT •
0
Entering edit mode

What hypothesis / question are you trying to answer?

ADD REPLY •
0
Entering edit mode

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

ADD REPLY •

Login before adding your answer.

Similar Posts
Loading Similar Posts
Traffic: 1809 users visited in the last hour
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6