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Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples

NIAID Data Ecosystem2026-03-09 收录

基因组诊断

拷贝数变异

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE73191 数据链接链接失效反馈

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资源简介：

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

应用场景：

创建时间：

2016-02-01

先天性心脏病

拷贝数变异

Array comparative genomic hybridization (aCGH) has led to an increased detection of causal chromosomal imbalances in individuals with congenital heart defects (CHD). The introduction of aCGH as a diag

DataCite Commons2020-09-02 更新120

Additional file 8 of Identification and population genetic analyses of copy number variations in six domestic goat breeds and Bezoar ibexes using next-generation sequencing

拷贝数变异

群体遗传学

Additional file 8: Table S6. Significantly enriched terms for the differentiation CNV genes identified in this study.

DataCite Commons2024-02-13 更新60

Additional file 1 of Detection of copy number variants in African goats using whole genome sequence data

基因组学

拷贝数变异

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

DataCite Commons2024-02-06 更新50

CNVRs Identified in Afghan Arabian Sheep Breeds.csv

基因组学

拷贝数变异

The CNVRs identified in Afghan sheep breeds: The aim of this study was to identify CNVs in 45 Afghan sheep consisting of three Arab, Baluchi, and Gedic breeds using genomic arrays containing 53862 sin

DataCite Commons2022-08-03 更新70

Table_1_Pan-Genomic Study of Mycobacterium tuberculosis Reflecting the Primary/Secondary Genes, Generality/Individuality, and the Interconversion Through Copy Number Variations.DOCX

分枝杆菌基因组与基因表达

拷贝数变异

Tuberculosis (TB) has surpassed HIV as the leading infectious disease killer worldwide since 2014. The main pathogen, Mycobacterium tuberculosis (Mtb), contains ~4,000 genes that account for ~90% of t

NIAID Data Ecosystem50

Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples

资源简介：

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