Brendan D O'Fallon

2 Questions 6 Answers 0 Followers

Questions related from Brendan D O'Fallon

Any recommendations for a good CNV detection tool?

I'm looking for a software tool to call copy number variations (CNV's) from NGS exome sequence data. There seem to be many possibilities (CNVnator, ExomeCNV, cn.MOPS, control-FREEC,...

07 July 2012 8,892 8 View

What's a good ranking algorithm for genetic variants associated with disease?

I realize it's a big topic, but I'd be curious to hear people's opinions about the best ways to rank genetic variants obtained from an NGS procedure by their probability of being disease causing....

05 May 2012 1,491 6 View