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Custom Agilent array-CGH of somatic cell hybrids targeted to 17q21.31 deletion syndrome locus

ChEBI2012-06-01 更新2026-07-21 收录

基因组拷贝数变异

染色体缺失综合征定位

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-34867 数据链接链接失效反馈

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Custom Agilent array-CGH of somatic cell hybrids targeted to 17q21.31 deletion syndrome locus

应用场景：

创建时间：

2012-06-01

基因组拷贝数变异

遗传性状分析

Recents studies in mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report the first gl

NIAID Data Ecosystem110

Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity [GenomeWideSNP_6]

基因组拷贝数变异

儿童肥胖遗传学

Purpose: Obesity is known to be a multifactorial condition that is highly heritable. There have been ~60 susceptibility loci identified, but they only account for a fraction of cases.. As copy number

NIAID Data Ecosystem90

Additional file 6: of A global analysis of CNVs in diverse yak populations using whole-genome resequencing

基因组拷贝数变异

牦牛遗传多样性

List of the potential 3154 CNVRs. (XLS 1175 kb)

Figshare2024-02-15 更新60

Genome-wide genic copy numbers for nine Macaca species based on 1kb windows

基因组拷贝数变异

猕猴基因组学

This is the genome-wide copy numbers (CNs) for every 1kb window in the genomes of nine Macaca species, including the Chinese rhesus (M. mulatta lasiota, CR), cynomolgus (M. fascicularis, CE), Tibetan

NIAID Data Ecosystem90

Genomic DNA sequencing and copy number estimation of RPE-1 and RPE-1 trisomic cells

基因组拷贝数变异

非整倍体细胞分子机制

This is part of the project "global quantification of cellular protein degradation". The data is used to show how protein levels change in response to gene copy number alterations in aneuploid cells.

NIAID Data Ecosystem70

Custom Agilent array-CGH of somatic cell hybrids targeted to 17q21.31 deletion syndrome locus

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