Convex_method_for_calling_CNVs_from_Exome_data___controls_
收藏NIAID Data Ecosystem2026-03-12 收录
官方服务:
资源简介:
Control data for CNV calling from whole exome data sets.
应用场景:
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.
DataCite Commons2022-06-27 更新90
Molecular karyotyping
CNVs detected in MMC-treated and untreated cells using molecular karyotyping. Raw data
NIAID Data Ecosystem70
Additional file 1 of Detection of copy number variants in African goats using whole genome sequence data
Additional file 1 Supplementary Table 1 Genes in CNV with VST values above the 99th percentile for each comparison. Supplementary Table 2 List of CNVR by population. Supplementary Table 3 Summary of C
Figshare2021-05-29 更新50
Canine diffuse large B-cell lymphoma (cDLBCL) whole-exome sequencing
Canine diffuse large B-cell lymphoma (cDLBCL) is the most extensive studied lymphoma subtype both in veterinary and comparative medicine because it represents a promising model of human DLBCL. Anyhow,
NIAID Data Ecosystem80
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]. Homo sapiens
Background: High-resolution microarray technology is routinely used in basic research and clinical practice to efficiently detect copy number variants (CNVs) across the entire human genome. A new gene
NIAID Data Ecosystem70



