uk10k_neuro_asd_tampere_rel_2012_07_05-sc-20120911 - samples
收藏NIAID Data Ecosystem2026-03-12 收录
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资源简介：
EGAD00001000232_UK10K_NEURO_ASD_TAMPERE_REL_2012_07_05EGA dataset EGAD00001000232
应用场景：
创建时间：
2021-04-23
相关数据集
uk10k_neuro_asd_skuse_rel_2012_07_05-sc-20120911 - samples
EGAD00001000231_UK10K_NEURO_ASD_SKUSE_REL_2012_07_05EGA dataset EGAD00001000231
NIAID Data Ecosystem60
Supplementary Material for: Whole Exome Sequencing of a multiplex family of Indian origin identifies variants in the RAI1 and FLII genes within the 17p11.2 region in siblings with autism and Smith Magenis Syndrome
Introduction: Autism Spectrum Disorders (ASDs) is a complex neurodevelopmental disorder characterized by restrictive repetitive behaviour and impairment in social and communication skills. It is extre
Figshare2024-05-17 更新20
Additional file 4 of Exploring autism spectrum disorder and co-occurring trait associations to elucidate multivariate genetic mechanisms and insights
Supplementary Table 1. Data and sample details of ASD and 8 genetically correlated traits (P < 0.05, calculated from LD Score Regression (LDSC)) are presented and applied towards multivariate-GWAS. Da
NIAID Data Ecosystem10
Copy number variation analysis in Japanese children with Autsim Spectrum Disorder by Affymetrix Genome-Wide Human SNP Array 6.0.
Autism spectrum disorder (ASD) is an innate neurodevelopmental disorder characterized by impairments in social communication/interaction, repetitive and restrictive behavior. Copy number variation (CN
NIAID Data Ecosystem30
Exome Sequencing in an Ancestrally Diverse Autism Cohort
Autism spectrum disorder (ASD) is a collection of neurodevelopmental disorders manifested by impaired social communication, repetitive behaviors, and restricted interests. We performed whole exome seq
NIAID Data Ecosystem20
