any tutorials for structural variants filtering and prioritization
Outputs from structural variants callers like breakdancer, lumpy and delly contains false positives.
How do you filter out those false positives and then prioritize the SVs? Anyone has a good resources or experiences on that ?
Thanks!
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Any idea how you would filter predictions from breakdancer?
One simple way is filter the output based on prediction score and read counts
# $9= prediction score
# $10= supporting reads
cat libraryP1.ctx | awk 'BEGIN {OFS="\t"} { if ($9 >= 40 && $10 >= 5) { print $0 }}' | wc -l
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Check out: http://bcb.io/2014/08/12/validated-whole-genome-structural-variation-detection-using-multiple-callers/
Personally, I find the builtin delly filter works reasonably well.
Thanks Heng for your reply! I happen to read this post before. I am wondering have you written any tutorials for that?