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资源简介：
ACGH 244K datasetEGA dataset EGAD00010000935
应用场景：
创建时间：
2017-07-26
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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De novo copy number variations in cloned dogs (Illumina SNP)
De novo copy number variations in cloned dogs (Illumina SNP)
ChEBI2013-12-17 更新50
Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer
Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer
ChEBI2010-05-26 更新30
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)
Figshare2020-08-27 更新50
Copy number variation analysis of human Barrett's esophagus stem cells
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
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