Observed type I errors at selected significance levels for the Generalised C-alpha test for association with a quantitative trait and a dichotomised version of a quantitative trait in a 50 kb region w

NIAID Data Ecosystem30

Burden test for KANL and ADSP unrelated datasets.

变异关联分析

基因负担检验

Collapsing and combine (CMC) test of rare variants by Fisher's exact test for (i) variants with a MAF≤1% and categorized to have a high or moderated effect (MAF≤1% HM) and (ii) singleton variants cate

Figshare2017-11-13 更新20

UK10K NEURO ASD GALLAGHER

自闭症谱系障碍遗传

变异关联分析

In the UK10K project we propose a series of complementary genetic approaches to find new low frequency/rare variants contributing to disease phenotypes. These will be based on obtaining the genome wid

NIAID Data Ecosystem50

Rare coding variants pinpoint genes that control human hematological traits

变异关联分析

血液学特征遗传学

The identification of rare coding or splice site variants remains the most straightforward strategy to link genes with human phenotypes. Here, we analyzed the association between 137,086 rare (minor a

NIAID Data Ecosystem30

SKAT results for the dataset grouped by data source.

资源简介：

相关数据集