Convex_method_for_calling_CNVs_from_Exome_data___controls_
收藏NIAID Data Ecosystem2026-03-12 收录
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资源简介：
Control data for CNV calling from whole exome data sets.
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创建时间：
2021-02-04
相关数据集
Additional file 3 of Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data
Additional file 3: Supplementary table 1.
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The recovery rates of each of the CNV-calling programs depending on CNV length based on data of Kidd et al.
*The pedigree information was incorporated with the calling of CNVs. Recovery rate was calculated with the requirement of copy number consistency.
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Additional file 7: of CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
Four amplified mutations in sample SA052. (XLS 23 kb)
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DNA methylation and copy number profiling in polymicrogyria. DNA methylation and copy number profiling in polymicrogyria
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