Is it possible to derive exon-size deletion/duplication information from target-enriched (array or in-solution), paired-end sequencing data ?
I'm working with a set of genes that frequently undergo partial and whole gene deletion duplications and would be grateful if I could derive this information from the sequencing data without having to also perform high-density CGH of each of the genes.
Is anyone working on a strategy for this ?
Thanks much !
I'm working with a set of genes that frequently undergo partial and whole gene deletion duplications and would be grateful if I could derive this information from the sequencing data without having to also perform high-density CGH of each of the genes.
Is anyone working on a strategy for this ?
Thanks much !
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