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CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing

Creator: Jiang, Yuchao, Wang, Rujin, Urrutia, Eugene, Anastopoulos, Ioannis N, Nathanson, Katherine L, Zhang, Nancy R

Abstract High-throughput DNA sequencing enables detection of copy number variations (CNVs) on the genome-wide scale with finer resolution compared to array-based methods but suffers from biases and artifacts that lead to false (more)

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13059_2018_1578_moesm1_esm.pdf

Collection: BioMed Central

Date Deposited: 2018-12-01

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Collection: BioMed Central

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13059_2018_article_1578.pdf

Collection: BioMed Central

Date Deposited: 2018-12-01

Date Created: 2018-12-01

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