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Genetic Copy Number Variants in Myocardial Infarction Patients with Hyperlipidemia

ChEBI2014-08-09 更新2026-07-21 收录

心血管疾病遗传学

拷贝数变异分析

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-31276 数据链接链接失效反馈

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Genetic Copy Number Variants in Myocardial Infarction Patients with Hyperlipidemia

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创建时间：

2014-08-09

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

FAIRsharing record for: Cancer Genome Mine

癌症基因组数据

拷贝数变异分析

This FAIRsharing record describes: Clinical information about tumor samples and microarray data, with emphasis on array comparative genomic hybridization (aCGH) and data mining of gene copy number ch

DataCite Commons2024-12-05 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

RiboSNitch in lncRNA H19 associated with Dilated Cardiomyopathy

RNA结构

心血管疾病遗传学

Secondary structure in the H19 transcript, which is altered through a SNP in DCM patients, is an attractive target for future studies investigating the molecular mechanism by which H19 contributes to

NIAID Data Ecosystem40

Genetic Copy Number Variants in Myocardial Infarction Patients with Hyperlipidemia

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