KOLF2.1J optical mapping data for structural variant identification. Homo sapiens
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1235749
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资源简介：
We aim to characterize the previously published reference human iPSC line KOLF2.1J, utilizing optical genome mapping to determine the likelihood of previously unidentified structural variants. We have identified a group of structural variants overlapping functional genes, which may warrant proper use and understanding of the KOLF2.1J line for specific applications.
创建时间：
2025-03-13
