I am not in need of any tool to discover CNVs.
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What is the most commonly used file format for storing Copy Number Variation data?
http://www.broadinstitute.org/igv/SEG
http://www.1000genomes.org/wiki/Analysis/Variant%20Call%20Format/vcf-variant-call-format-version-41
DNAcopy output is very common - 6col (sample, chr, start, stop, num.probes, seg.mean)
CNVnator: http://www.ncbi.nlm.nih.gov/pubmed/21324876 Download: http://sv.gersteinlab.org/
I am not in need of any tool to discover CNVs.
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