August 31, 2012Open Access

A robust model for read count data in exome sequencing experiments and implications for copy number variant calling

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Abstract

The code used in this analysis has been implemented into an R package called ExomeDepth and is available at the Comprehensive R Archive Network (CRAN).

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Plagnol et al. (Fri,) studied this question.

synapsesocial.com/papers/69d7cb917392c8ce61bedd76 https://doi.org/https://doi.org/10.1093/bioinformatics/bts526

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