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SIRT6 hMSC genome sequencing for CNV study. Homo sapiens

NIAID Data Ecosystem2026-03-08 收录

基因敲除模型

拷贝数变异分析

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA288062 数据链接链接失效反馈

官方服务：

资源简介：

Our goal is to build a SIRT6 deleted human model cell lines and study the effect of SIRT6 deficiency on DNA stability.

应用场景：

创建时间：

2015-06-25

葡萄膜黑色素瘤基因

拷贝数变异分析

Primary uveal melanomas show multiple chromosomal aberrations. To identify genome variation in six human primary uveal melanomas, genome wide copy number variation (CNV) analyses were carried out in h

NIAID Data Ecosystem60

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig5a]. Mus musculus

拷贝数变异分析

免疫编辑基因组学

Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma

NIAID Data Ecosystem30

Table S2 : Consistently divergent CNVs in the Focal Test from The role of copy-number variation in the reinforcement of sexual isolation between the two European subspecies of the house mouse

性隔离与物种形成

拷贝数变异分析

this file is in .txt format

The Royal Society Figshare2020-07-13 更新30

Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study

1型糖尿病遗传

拷贝数变异分析

Type 1 Diabetes Genetics Consortium (T1DGC) was formed to address issues of limited sample size and consistency of phenotyping that had limited genetic investigations on risk of type 1 diabetes (T1D).

NIAID Data Ecosystem50

Colorectal cancer BB copy number arrays

结直肠癌基因组学

拷贝数变异分析

Colorectal cancer BB copy number arrays

ChEBI2014-12-22 更新30