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Cytogenetics 2.7M and Cytoscan HD 2.8M Microarrays in autistic families in the Lebanese population

ChEBI2017-07-24 更新2026-07-12 收录

自闭症遗传学

基因组拷贝数变异

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-4963 数据链接链接失效反馈

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Cytogenetics 2.7M and Cytoscan HD 2.8M Microarrays in autistic families in the Lebanese population

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创建时间：

2017-07-24

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

Genomic evidence for multifactorial inheritance in autism

自闭症遗传学

多基因性状遗传

Autism spectrum disorder (ASD) is a common highly heritable disorder with multifactorial influences.

DataCite Commons2023-05-16 更新70

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

Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021529]

基因组拷贝数变异

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 Ecosystem80

Cytogenetics 2.7M and Cytoscan HD 2.8M Microarrays in autistic families in the Lebanese population

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