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The fine-scale and complex architecture of human copy number variation

ChEBI2008-01-23 更新2026-07-21 收录

拷贝数变异分析

基因组结构变异

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-9831 数据链接链接失效反馈

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资源简介：

The fine-scale and complex architecture of human copy number variation

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创建时间：

2008-01-23

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

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

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

Output from GRIMM showing the most parsimonious reversal scenario.

基因组结构变异

比较基因组学

Each number represents an LCB calculated by MAUVE between CA88 and CO92. Changes between steps are underlined. Negative numbers represent an inverted LCB.

Figshare2015-12-02 更新30

The fine-scale and complex architecture of human copy number variation

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