FunSeq2 - A flexible framework to prioritize regulatory mutations from cancer genome sequencing
Retrieve Result

Four output files will be generated :

1. A detailed output file

2. A candidate variants file, including coding (nonsynonymous and premature stop) variants, noncoding variants (score >=1.5), and variants associated with cancer genes

3. A summary file for recurrent analysis if multiple-sample data are uploaded [Optional]

4. An error file

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