DSD gene variants. Each variant found in a diagnostic gene (after the filtering and curation process) is shown. In some cases where the gene is inherited in an autosomal recessive manner, two variants

Figshare2016-12-14 更新40

Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis

肌萎缩侧索硬化症遗传研究

全基因组测序变异分析

The contribution of genetic and environmental factors to the pathogenesis of sporadic amyotrophic lateral sclerosis (ALS) remains unclear. To investigate the genetic component of the disease, we perfo

NIAID Data Ecosystem40

Whole Genome Sequencing yjhX mutant screen. Whole Genome Sequencing yjhX mutant screen

全基因组测序变异分析

功能基因组筛选

The trans-acting mutant genetic selection was performed as described in Baniulyte et al, 2017. Chromosomal mutations were identified by whole genome sequencing.

NIAID Data Ecosystem50

deCODE Genetics Whole-Genome Sequencing Variants

全基因组测序变异分析

冰岛人群遗传变异

Autosomal sequence variants identified in deCODE's whole-genome sequencing of 2,636 Icelanders

NIAID Data Ecosystem40