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Additional file 4: of CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing

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posted on 2018-11-26, 05:00 authored by Yuchao Jiang, Rujin Wang, Eugene Urrutia, Ioannis Anastopoulos, Katherine Nathanson, Nancy Zhang
Table S3. WES CNV calls from the 1000 Genomes Project. (XLSX 1263 kb)

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National Institutes of Health

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    Genome Biology

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    Copy number variationNormalizationNext-generation sequencingLatent factorNegative control

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