Copy number variation (CNV) makes a major contribution to overall genetic variation and is suspected to play an important role in adaptation. However, aside from a few model species, the extent of CNV

NIAID Data Ecosystem50

Additional file 4 of Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models

乳腺癌基因组学

拷贝数变异分析

Additional file 4: Table S7. Comparison of the genes with copy number alterations in COSMIC, Ben-David et al and this study.

NIAID Data Ecosystem40

Copy number changes identified through WGS.

拷贝数变异分析

基因组测序

aFocal gains/losses are defined as CNVs occurring across regions that are

Figshare2015-12-02 更新60

Additional file 2: of Ioncopy: an R Shiny app to call copy number alterations in targeted NGS data

拷贝数变异分析

靶向测序生物信息学

Breast cancer example data set. Coverage matrix of 152 amplicons (48 genes) in 184 breast cancer samples. (XLS 196Â kb)

Figshare2018-04-27 更新50

Array_FL_dataset_11

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