Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples. Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples
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下载链接:
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA296348
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资源简介:
This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
创建时间:
2015-09-18



