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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

Identifying shared genetic factors underlying epilepsy and congenital heart  disease in Europeans | Human Genetics
Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans | Human Genetics

sumSTAAR: A flexible framework for gene-based association studies using  GWAS summary statistics | PLOS Computational Biology
sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics | PLOS Computational Biology

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

The genetics of idiopathic intracranial hypertension (IIH): Integration of  population studies and clinical data | medRxiv
The genetics of idiopathic intracranial hypertension (IIH): Integration of population studies and clinical data | medRxiv

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

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

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

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

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

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

Genetic Rare-Variant Test
Genetic Rare-Variant Test

Manhattan Plot of SKAT-O association results: Each point represents one...  | Download Scientific Diagram
Manhattan Plot of SKAT-O association results: Each point represents one... | Download Scientific Diagram

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

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

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

Scatter plots of association P-values from SAIGE-GENE versus SMMAT and... |  Download Scientific Diagram
Scatter plots of association P-values from SAIGE-GENE versus SMMAT and... | Download Scientific Diagram

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 | 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

Table 1 | PLOS Genetics
Table 1 | PLOS Genetics

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

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

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