![PDF] Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT). | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/dd16ad168f2be8f923bcab7cdafcc9f6a7d76767/17-Figure1-1.png "PDF] Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT). | Semantic Scholar")
PDF] Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT). | Semantic Scholar
Combined genotype and haplotype tests for region-based association studies | BMC Genomics | Full Text
Scatter plots of association P-values from SAIGE-GENE versus SMMAT and... | Download Scientific Diagram
Rare genetic variants not the major contributing factors to common diseases
Frontiers | Recent advances and challenges of rare variant association analysis in the biobank sequencing era
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests | Nature Genetics
Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection | PNAS
Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic | PLOS Genetics
Genetic signature of human longevity in PKC and NF‐κB signaling - Ryu - 2021 - Aging Cell - Wiley Online Library
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort | Neurology
Set-based rare variant association tests for biobank scale sequencing data sets | medRxiv
Significant genes in the sequence kernel association test (SKAT)... | Download Scientific Diagram
Frontiers | Association Study of Genetic Variants in Autophagy Pathway and Risk of Non-syndromic Cleft Lip With or Without Cleft Palate
Manhattan Plot of SKAT-O association results: Each point represents one... | Download Scientific Diagram
High-throughput sequencing analysis of nuclear-encoded mitochondrial genes reveals a genetic signature of human longevity | GeroScience
GitHub - lin-lab/SKAT: Functions for kernel-regression-based association tests including Burden test, SKAT and SKAT-O. These methods aggregate individual SNP score statistics in a SNP set and efficiently compute SNP-set level p-values.
Rare Variant Analysis - Module 1 - YouTube
A phenome-wide scan reveals convergence of common and rare variant associations | Genome Medicine | Full Text
Stat Genetics Online Videos – Statistical Genetics
Genetic Rare-Variant Test
Frontiers | Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer
Family-based gene-environment interaction using sequence kernel association test (FGE-SKAT) for complex quantitative traits | Scientific Reports
An allelic-series rare-variant association test for candidate-gene discovery - ScienceDirect
Impact of rare and common genetic variation in the Interleukin-1 pathway on human cytokine responses | bioRxiv
Discovered genes with the SKAT-O gene aggregate tests. A. Minimal... | Download Scientific Diagram
