These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 37158367)
1. Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes. Bocher O; Marenne G; Génin E; Perdry H Genet Epidemiol; 2023 Sep; 47(6):450-460. PubMed ID: 37158367 [TBL] [Abstract][Full Text] [Related]
2. Extension of SKAT to multi-category phenotypes through a geometrical interpretation. Bocher O; Marenne G; Tournier-Lasserve E; ; Génin E; Perdry H Eur J Hum Genet; 2021 May; 29(5):736-744. PubMed ID: 33446828 [TBL] [Abstract][Full Text] [Related]
3. Rare variant association testing for multicategory phenotype. Bocher O; Marenne G; Saint Pierre A; Ludwig TE; Guey S; Tournier-Lasserve E; Perdry H; Génin E Genet Epidemiol; 2019 Sep; 43(6):646-656. PubMed ID: 31087445 [TBL] [Abstract][Full Text] [Related]
4. RVFam: an R package for rare variant association analysis with family data. Chen MH; Yang Q Bioinformatics; 2016 Feb; 32(4):624-6. PubMed ID: 26508760 [TBL] [Abstract][Full Text] [Related]
5. Powerful rare variant association testing in a copula-based joint analysis of multiple phenotypes. Konigorski S; Yilmaz YE; Janke J; Bergmann MM; Boeing H; Pischon T Genet Epidemiol; 2020 Jan; 44(1):26-40. PubMed ID: 31732979 [TBL] [Abstract][Full Text] [Related]
6. CollapsABEL: an R library for detecting compound heterozygote alleles in genome-wide association studies. Zhong K; Karssen LC; Kayser M; Liu F BMC Bioinformatics; 2016 Apr; 17():156. PubMed ID: 27059780 [TBL] [Abstract][Full Text] [Related]
7. Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score. Bocher O; Ludwig TE; Oglobinsky MS; Marenne G; Deleuze JF; Suryakant S; Odeberg J; Morange PE; Trégouët DA; Perdry H; Génin E PLoS Genet; 2022 Sep; 18(9):e1009923. PubMed ID: 36112662 [TBL] [Abstract][Full Text] [Related]
8. RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method. Hamazaki K; Iwata H PLoS Comput Biol; 2020 Feb; 16(2):e1007663. PubMed ID: 32059004 [TBL] [Abstract][Full Text] [Related]
9. Gene-based segregation method for identifying rare variants in family-based sequencing studies. Qiao D; Lange C; Laird NM; Won S; Hersh CP; Morrow J; Hobbs BD; Lutz SM; Ruczinski I; Beaty TH; Silverman EK; Cho MH Genet Epidemiol; 2017 May; 41(4):309-319. PubMed ID: 28191685 [TBL] [Abstract][Full Text] [Related]
11. Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits. Oualkacha K; Lakhal-Chaieb L; Greenwood CM Int J Epidemiol; 2016 Apr; 45(2):402-7. PubMed ID: 27085080 [TBL] [Abstract][Full Text] [Related]
12. G2P: a Genome-Wide-Association-Study simulation tool for genotype simulation, phenotype simulation and power evaluation. Tang Y; Liu X Bioinformatics; 2019 Oct; 35(19):3852-3854. PubMed ID: 30848784 [TBL] [Abstract][Full Text] [Related]
13. MATICCE: mapping transitions in continuous character evolution. Hipp AL; Escudero M Bioinformatics; 2010 Jan; 26(1):132-3. PubMed ID: 19880368 [TBL] [Abstract][Full Text] [Related]
14. Protocol for Construction of Genome-Wide Epistatic SNP Networks Using WISH-R Package. Kadarmideen HN; Carmelo VAO Methods Mol Biol; 2021; 2212():155-168. PubMed ID: 33733355 [TBL] [Abstract][Full Text] [Related]
15. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Fan R; Chiu CY; Jung J; Weeks DE; Wilson AF; Bailey-Wilson JE; Amos CI; Chen Z; Mills JL; Xiong M Genet Epidemiol; 2016 Dec; 40(8):702-721. PubMed ID: 27374056 [TBL] [Abstract][Full Text] [Related]
16. deTS: tissue-specific enrichment analysis to decode tissue specificity. Pei G; Dai Y; Zhao Z; Jia P Bioinformatics; 2019 Oct; 35(19):3842-3845. PubMed ID: 30824912 [TBL] [Abstract][Full Text] [Related]
17. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease. Persyn E; Karakachoff M; Le Scouarnec S; Le Clézio C; Campion D; Consortium FE; Schott JJ; Redon R; Bellanger L; Dina C PLoS One; 2017; 12(7):e0179364. PubMed ID: 28742119 [TBL] [Abstract][Full Text] [Related]
18. The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants. Aref L; Bastarache L; Hughey JJ Bioinformatics; 2022 Oct; 38(21):4972-4974. PubMed ID: 36083022 [TBL] [Abstract][Full Text] [Related]
19. Rare variant association test in family-based sequencing studies. Wang X; Zhang Z; Morris N; Cai T; Lee S; Wang C; Yu TW; Walsh CA; Lin X Brief Bioinform; 2017 Nov; 18(6):954-961. PubMed ID: 27677958 [TBL] [Abstract][Full Text] [Related]
20. Reproducible simulations of realistic samples for next-generation sequencing studies using Variant Simulation Tools. Peng B Genet Epidemiol; 2015 Jan; 39(1):45-52. PubMed ID: 25395236 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]