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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.
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 Association Analysis: Study Designs and Statistical Tests -  ScienceDirect
Rare-Variant Association Analysis: Study Designs and Statistical Tests - ScienceDirect

Rare variant association analysis: SKAT, SKAT-O, Burden test – 두마디 정밀의료
Rare variant association analysis: SKAT, SKAT-O, Burden test – 두마디 정밀의료

Frontiers | Exome-Wide Rare Variant Analysis From the DiscovEHR Study  Identifies Novel Candidate Predisposition Genes for Endometrial Cancer
Frontiers | Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer

The mean power of SKAT-O across different genetic architectures using... |  Download Scientific Diagram
The mean power of SKAT-O across different genetic architectures using... | Download Scientific Diagram

Mutational Analysis of Known ALS Genes in an Italian Population-Based  Cohort | Neurology
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort | Neurology

An allelic-series rare-variant association test for candidate-gene  discovery - ScienceDirect
An allelic-series rare-variant association test for candidate-gene discovery - ScienceDirect

Genes | Free Full-Text | Assessment of Rare Genetic Variants to Identify  Candidate Modifier Genes Underlying Neurological Manifestations in  Neurofibromatosis 1 Patients
Genes | Free Full-Text | Assessment of Rare Genetic Variants to Identify Candidate Modifier Genes Underlying Neurological Manifestations in Neurofibromatosis 1 Patients

Frontiers | Association Study of Genetic Variants in Autophagy Pathway and  Risk of Non-syndromic Cleft Lip With or Without Cleft Palate
Frontiers | Association Study of Genetic Variants in Autophagy Pathway and Risk of Non-syndromic Cleft Lip With or Without Cleft Palate

Combined genotype and haplotype tests for region-based association studies  | BMC Genomics | Full Text
Combined genotype and haplotype tests for region-based association studies | BMC Genomics | Full Text

A phenome-wide scan reveals convergence of common and rare variant  associations | Genome Medicine | Full Text
A phenome-wide scan reveals convergence of common and rare variant associations | Genome Medicine | Full Text

Impact of rare and common genetic variation in the Interleukin-1 pathway on  human cytokine responses | bioRxiv
Impact of rare and common genetic variation in the Interleukin-1 pathway on human cytokine responses | bioRxiv

BayesKAT: Bayesian Optimal Kernel-based Test for genetic association  studies reveals joint genetic effects in complex diseases | bioRxiv
BayesKAT: Bayesian Optimal Kernel-based Test for genetic association studies reveals joint genetic effects in complex diseases | bioRxiv

Genes | Free Full-Text | Identifying Rare Genetic Variants of Immune  Mediators as Risk Factors for Autism Spectrum Disorder
Genes | Free Full-Text | Identifying Rare Genetic Variants of Immune Mediators as Risk Factors for Autism Spectrum Disorder

Set-based rare variant association tests for biobank scale sequencing data  sets | medRxiv
Set-based rare variant association tests for biobank scale sequencing data sets | medRxiv

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

Impact of natural selection on global patterns of genetic variation and  association with clinical phenotypes at genes involved in SARS-CoV-2  infection | PNAS
Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection | PNAS

High-throughput sequencing analysis of nuclear-encoded mitochondrial genes  reveals a genetic signature of human longevity | GeroScience
High-throughput sequencing analysis of nuclear-encoded mitochondrial genes reveals a genetic signature of human longevity | GeroScience

Genetic signature of human longevity in PKC and NF‐κB signaling - Ryu -  2021 - Aging Cell - Wiley Online Library
Genetic signature of human longevity in PKC and NF‐κB signaling - Ryu - 2021 - Aging Cell - Wiley Online Library

PWAS and SKAT provide complementary results. a Number of significant... |  Download Scientific Diagram
PWAS and SKAT provide complementary results. a Number of significant... | Download Scientific Diagram

Rare Variant Analysis - Module 1 - YouTube
Rare Variant Analysis - Module 1 - YouTube

Rare Variant Analysis - Module 1 - YouTube
Rare Variant Analysis - Module 1 - YouTube

Two-phase SSU and SKAT in genetic association studies | Journal of Genetics
Two-phase SSU and SKAT in genetic association studies | Journal of Genetics

Population-Based DNA Variant Analysis | PPT
Population-Based DNA Variant Analysis | PPT