A copy number variation detection methods based on low coverage sequencing. Homo sapiens
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA203442
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资源简介：
We developed an sensitively and reliably detect CNVs method using low coverage or even ultra-low coverage data through population-scale sequencing.
创建时间：
2013-05-18
