首页/数据集/Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR

Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR

NIAID Data Ecosystem2026-03-07 收录

拷贝数变异

精神发育迟滞遗传学

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA137289 数据链接链接失效反馈

官方服务：

资源简介：

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

应用场景：

创建时间：

2011-02-16

基因重复分析

拷贝数变异

VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.

NIAID Data Ecosystem90

Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]. Homo sapiens

拷贝数变异

微阵列平台

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

Additional file 8: Table S6. of Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases

神经干细胞

拷贝数变异

De novo copy number variations (CNVs) identified in the 1201C1 iPSC-derived NSPCs. (XLSX 35Â kb)

DataCite Commons2024-12-17 更新70

Molecular karyotyping

拷贝数变异

药物诱导基因组不稳定性

CNVs detected in MMC-treated and untreated cells using molecular karyotyping. Raw data

NIAID Data Ecosystem70

Additional file 4 of Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome