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Somatic copy number variation profiling in matched brain and extracranial metastases of melanoma

ChEBI2014-05-08 更新2026-07-21 收录

黑色素瘤转移基因组学

拷贝数变异分析

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-50495 数据链接链接失效反馈

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Somatic copy number variation profiling in matched brain and extracranial metastases of melanoma

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创建时间：

2014-05-08

拷贝数变异分析

纯合性分析

These samples include 4 patients with a triplication/ROH combination on: (1) chromosome 6, (2) chromosom 9, (3) chromosome 10, (4) chromosome 14 All arrays contain single hybridisations of either pati

NIAID Data Ecosystem130

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

927dfa8a-2c43-4c84-8ac0-ff8261064165 - samples

黑色素瘤转移基因组学

靶向药物响应转录组学

Whole genome sequencing of cutaneous melanoma skin and brain metastases and matched normal DNA, as well as RNA sequencing of material from the skin and brain metastases. In addition, RNA sequencing wa

NIAID Data Ecosystem40

Additional file 3 of Copy number variation in human genomes from three major ethno-linguistic groups in Africa

拷贝数变异分析

群体基因组学

Additional file 3: Table S2. GenomeSTRiP CNVR that intersect cn.MOPS CNVR after QC.

Figshare2020-04-10 更新80

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

Somatic copy number variation profiling in matched brain and extracranial metastases of melanoma

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