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资源简介：
aCGH raw data submitted to Gene Expression Omnibus
应用场景：
创建时间：
2015-01-01
相关数据集
Supplementary Material for: Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human
At present, low-pass whole-genome sequencing (WGS) is frequently used in clinical research and in the screening of copy number variations (CNVs). However, there are still some challenges in the detect
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Additional file 4 of Copy number variation of microRNA genes in the human genome
Additional file 4:miRNAs located in CNVs with well defined breakpoints. Excel table showing characteristics of miRNAs located in CNVs with well defined breakpoints. (XLS 14 KB)
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Twenty genes commonly identified by literature review and analysis of two microarray datasets.
Twenty genes commonly identified by literature review and analysis of two microarray datasets.
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MADSCAN evaluation using heart disease patients
Data set for microarray data processing tool evaluation. Patients affected by valvular heart disease and coronary artery disease, or idiopathic dilated cardiomyopathy. Keywords = Myochip Keywords = MA
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De novo copy number variations in cloned dogs (Illumina SNP)
De novo copy number variations in cloned dogs (Illumina SNP)
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