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.
![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](https://www.frontiersin.org/files/Articles/456684/fonc-09-00574-HTML-r1/image_m/fonc-09-00574-g001.jpg)
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](https://www.researchgate.net/publication/332991102/figure/fig4/AS:756999251845122@1557494094584/The-mean-power-of-SKAT-O-across-different-genetic-architectures-using-imputed-data.png)
The mean power of SKAT-O across different genetic architectures using... | Download Scientific Diagram
![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](https://pub.mdpi-res.com/genes/genes-13-02218/article_deploy/html/images/genes-13-02218-g001-550.jpg?1669711807)
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](https://www.frontiersin.org/files/Articles/560254/fcell-08-00576-HTML/image_m/fcell-08-00576-g001.jpg)
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](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2F1471-2164-14-569/MediaObjects/12864_2013_Article_5387_Fig3_HTML.jpg)
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](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs13073-023-01253-9/MediaObjects/13073_2023_1253_Fig1_HTML.png)
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](https://www.biorxiv.org/content/biorxiv/early/2020/04/01/2020.02.14.949602/F4.large.jpg)
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](https://www.biorxiv.org/content/biorxiv/early/2023/10/20/2023.10.18.562824/F5.large.jpg)
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](https://pub.mdpi-res.com/genes/genes-13-01098/article_deploy/html/images/genes-13-01098-g001.png?1655874438)
Genes | Free Full-Text | Identifying Rare Genetic Variants of Immune Mediators as Risk Factors for Autism Spectrum Disorder
![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](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
![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](https://www.pnas.org/cms/10.1073/pnas.2123000119/asset/697b5a61-9191-4f3a-ac6c-2e7243bf5491/assets/images/large/pnas.2123000119fig06.jpg)
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](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs11357-022-00634-z/MediaObjects/11357_2022_634_Fig4_HTML.png)
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](https://onlinelibrary.wiley.com/cms/asset/1537fd6d-ed78-4603-80c8-a619aaef7e59/acel13362-fig-0001-m.jpg)
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](https://www.researchgate.net/publication/342930103/figure/fig3/AS:913399722561536@1594782872059/PWAS-and-SKAT-provide-complementary-results-a-Number-of-significant-genes-detected-by.png)