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Profiling DNA copy number alterations of myxofibrosarcomas with NimbleGen array CGH chips

ChEBI2012-02-02 更新2026-07-21 收录

肉瘤基因组学

拷贝数变异分析

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-35483 数据链接链接失效反馈

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资源简介：

Profiling DNA copy number alterations of myxofibrosarcomas with NimbleGen array CGH chips

应用场景：

创建时间：

2012-02-02

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

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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).

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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

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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

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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.

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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.

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