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Old 07-27-2012, 09:19 AM   #1
shuteo
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Location: singapore

Join Date: Jul 2012
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Default Copy number variation: read depth algorithms and BAF

Does anyone know of depth of coverage or read depth algorithms that incoporates information on heterozygosity (like B allele frequency as is commonly used for SNP array algorithms such as QuantiSNP and PennCNV)?
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