官方服务：
资源简介：
Processed TCGA CNV data
应用场景：
创建时间：
2022-02-17
相关数据集
Array CGH analysis of human uveal melanomas. Array CGH analysis of human uveal melanomas
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
Additional file 2 of Whole genome copy number analyses reveal a highly aberrant genome in TP53 mutant lung adenocarcinoma tumors
Additional file 2. Recurrent aberrant regions and associated genes.
Figshare2021-10-09 更新40
An integrated genomics approach for novel biomarker discovery in squamous cell cervical carcinoma. Homo sapiens
Detection of copy number dependent gene expression profiles in epithelial tumours has lead to the discovery of genes significant in diagnosis, prognosis and of therapeutic value. We sought to apply th
NIAID Data Ecosystem30
Rare CNVs identified in 82 patients with pulmonary atresia.
P, pathogenic; UK, unknown; PP, potentially pathogenic.
NIAID Data Ecosystem50
