遇见数据集

Genes found to be mutated in exomes of 15 CB iPSC lines.

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NIAID Data Ecosystem2026-03-07 收录
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The full details of each SNV including reads of SNV and wildtype alleles are in Table S1. MK: iPSC lines generated with OCT4, SOX2, MYC and KLF4; OS: iPSC lines generated with OCT4 and SOX2; Z: iPSC lines generated with OCT4, SOX2 and ZSCAN4. CDS: coding sequence; UTR: untranslated region; Downstream: SNV is at downstream of 5′UTR; S: synonymous coding mutation; NS: nonsynonymous coding mutation.

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2013-04-01
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