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Copy number variation in the bovine genome
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创建时间：
2010-04-22
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
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
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
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
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.
P, pathogenic; UK, unknown; PP, potentially pathogenic.
NIAID Data Ecosystem50
