Homo sapiens Random survey
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下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP015736
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资源简介：
Restriction site associated DNA (RAD) sequencing was used for measurement of coverage and minor allele frequency for copy number analysis. And through comparing to other re-sequencing strategies cost-effective and comprehensive analysis of CNVs was done.
创建时间：
2017-11-21
