I am testing few CNV tools for WGS dataset (short reads Illumina). Few tools working on: GenomeStrip, cn.mops, Delly, ERDS, Lumpy, Ulysses. Do you have any suggestion further?
CNVnator and cn.MOPS are good starting points. Also look at Pindel to find smaller duplications and deletions.
If you're able to run multiple callers, consider using MetaSV to consolidate the results from all callers. This will improve your accuracy at all scales and simplify the rest of your analysis by combining the calls into a single VCF.
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updated 4.3 years ago by
Ram
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written 10.1 years ago by
Eric T.
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Thank you Etal
CNVnator gives an error : "Too many arguments".
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updated 4.3 years ago by
Ram
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written 9.5 years ago by
rse
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There are multiple tools, i used varscan2/GISTIC. I wrote a tutorial here: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in population.