SNP array data for Wilms Tumor harboring de novo germline mutation in CTCF
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接：
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE193017
下载链接
链接失效反馈官方服务：
资源简介：
SNP array was combined with next generation sequencing (NGS) to identify a unique de novo germline mutation in CTCF that became homozygous in the tumor. SNP array shows an LOH through chr16q where CTCF is located. CytoScan HD arrays (Affymetrix) were performed according to the manufacturer's directions on DNA extracted from Wilms tumor sample.
创建时间：
2022-04-27
