Hi,
Wondering if there has been any reports of multiple samples comparison done for variants?
Say in the TCGA or 100 exomes projects from different centres, has anyone developed scripts to compare multiple samples, weighted on their coverage and confidence scores?
This would be also useful for segregation analyses in Mendelian disorders... to follow up linkage.
Wondering if there has been any reports of multiple samples comparison done for variants?
Say in the TCGA or 100 exomes projects from different centres, has anyone developed scripts to compare multiple samples, weighted on their coverage and confidence scores?
This would be also useful for segregation analyses in Mendelian disorders... to follow up linkage.
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