Homo sapiens Exome.SRP019719
收藏DataCite Commons2020-10-10 更新2025-04-09 收录
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https://db.cngb.org/search/project/CNPhis0000476/
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资源简介：
To facilitate the clinical implementation of genomic medicine by next-generation sequencing, it will be critically important to obtain accurate and consistent variant calls on personal genomes. Multiple software tools for variant calling are available, but it is unclear how comparable these tools are or what their relative merits in real-world scenarios might be.
提供机构：
CNGB
创建时间：
2018-10-20
