whole exome sequence of NSCLC patients

NIAID Data Ecosystem2026-05-01 收录

非小细胞肺癌体细胞突变分析

拷贝数变异分析

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1095562 数据链接链接失效反馈

官方服务：

资源简介：

Confirmation of somatic mutation and copy number variation of patient-derived cells of NSCLC patients

创建时间：

2024-04-02

Array CGH analysis of human uveal melanomas. Array CGH analysis of human uveal melanomas

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

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

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

Additional file 2 of MetaCNV - a consensus approach to infer accurate copy numbers from low coverage data

癌症基因组数据

拷贝数变异分析

Additional file 2. CCLs knownCNVs Supplementary table containing genes per cancer cell line, incl. Copy number, segment length and evaluation length.

Figshare2020-06-03 更新50

Rare CNVs identified in 82 patients with pulmonary atresia.

肺动脉闭锁遗传学

拷贝数变异分析

P, pathogenic; UK, unknown; PP, potentially pathogenic.

NIAID Data Ecosystem50