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WIG file support

I have 777k Illumina SNP chip genotypes of the same individuals that have now been sequenced, I have been using CNAM to call CNVs from chip data and exported wiggle tracks for each individual and from multivariate analysis. It would be great to be able to load them as annotation tracks to visually assess consensus with read depth information from NGS data, at the moment when I try loading a wiggle file GenomeBrowse crashes.