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.
3. Testing genetic association with rare and common variants in family data. Chen H; Malzahn D; Balliu B; Li C; Bailey JN Genet Epidemiol; 2014 Sep; 38 Suppl 1(0 1):S37-43. PubMed ID: 25112186 [TBL] [Abstract][Full Text] [Related]
4. Challenges of linkage analysis in the era of whole-genome sequencing. Santorico SA; Edwards KL Genet Epidemiol; 2014 Sep; 38 Suppl 1():S92-6. PubMed ID: 25112196 [TBL] [Abstract][Full Text] [Related]
5. Rare variant detection using family-based sequencing analysis. Peng G; Fan Y; Palculict TB; Shen P; Ruteshouser EC; Chi AK; Davis RW; Huff V; Scharfe C; Wang W Proc Natl Acad Sci U S A; 2013 Mar; 110(10):3985-90. PubMed ID: 23426633 [TBL] [Abstract][Full Text] [Related]
6. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Chiu CY; Jung J; Wang Y; Weeks DE; Wilson AF; Bailey-Wilson JE; Amos CI; Mills JL; Boehnke M; Xiong M; Fan R Genet Epidemiol; 2017 Jan; 41(1):18-34. PubMed ID: 27917525 [TBL] [Abstract][Full Text] [Related]
7. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction. DE LA Vega FM; Bustamante CD; Leal SM Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034 [TBL] [Abstract][Full Text] [Related]
8. A robust model-free approach for rare variants association studies incorporating gene-gene and gene-environmental interactions. Fan R; Lo SH PLoS One; 2013; 8(12):e83057. PubMed ID: 24358248 [TBL] [Abstract][Full Text] [Related]
9. Molecular genetic studies of complex phenotypes. Marian AJ Transl Res; 2012 Feb; 159(2):64-79. PubMed ID: 22243791 [TBL] [Abstract][Full Text] [Related]
10. Clinical assessment incorporating a personal genome. Ashley EA; Butte AJ; Wheeler MT; Chen R; Klein TE; Dewey FE; Dudley JT; Ormond KE; Pavlovic A; Morgan AA; Pushkarev D; Neff NF; Hudgins L; Gong L; Hodges LM; Berlin DS; Thorn CF; Sangkuhl K; Hebert JM; Woon M; Sagreiya H; Whaley R; Knowles JW; Chou MF; Thakuria JV; Rosenbaum AM; Zaranek AW; Church GM; Greely HT; Quake SR; Altman RB Lancet; 2010 May; 375(9725):1525-35. PubMed ID: 20435227 [TBL] [Abstract][Full Text] [Related]
11. Association studies for next-generation sequencing. Luo L; Boerwinkle E; Xiong M Genome Res; 2011 Jul; 21(7):1099-108. PubMed ID: 21521787 [TBL] [Abstract][Full Text] [Related]
12. A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data. Wang P; Rahman M; Jin L; Xiong M BMC Genomics; 2016 Nov; 17(1):881. PubMed ID: 27821073 [TBL] [Abstract][Full Text] [Related]
13. Longitudinal data analysis for genetic studies in the whole-genome sequencing era. Wu Z; Hu Y; Melton PE Genet Epidemiol; 2014 Sep; 38 Suppl 1():S74-80. PubMed ID: 25112193 [TBL] [Abstract][Full Text] [Related]
14. Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data. Cooper GM; Shendure J Nat Rev Genet; 2011 Aug; 12(9):628-40. PubMed ID: 21850043 [TBL] [Abstract][Full Text] [Related]
15. Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data. Li B; Wei Q; Zhan X; Zhong X; Chen W; Li C; Haines J PLoS Genet; 2015 Jun; 11(6):e1005271. PubMed ID: 26043085 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets. Pope BJ; Nguyen-Dumont T; Odefrey F; Hammet F; Bell R; Tao K; Tavtigian SV; Goldgar DE; Lonie A; Southey MC; Park DJ BMC Bioinformatics; 2013 Feb; 14():65. PubMed ID: 23441864 [TBL] [Abstract][Full Text] [Related]
18. Clinical interpretation and implications of whole-genome sequencing. Dewey FE; Grove ME; Pan C; Goldstein BA; Bernstein JA; Chaib H; Merker JD; Goldfeder RL; Enns GM; David SP; Pakdaman N; Ormond KE; Caleshu C; Kingham K; Klein TE; Whirl-Carrillo M; Sakamoto K; Wheeler MT; Butte AJ; Ford JM; Boxer L; Ioannidis JP; Yeung AC; Altman RB; Assimes TL; Snyder M; Ashley EA; Quertermous T JAMA; 2014 Mar; 311(10):1035-45. PubMed ID: 24618965 [TBL] [Abstract][Full Text] [Related]
19. Rare variant association test with multiple phenotypes. Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885 [TBL] [Abstract][Full Text] [Related]
20. Genome analysis and knowledge-driven variant interpretation with TGex. Dahary D; Golan Y; Mazor Y; Zelig O; Barshir R; Twik M; Iny Stein T; Rosner G; Kariv R; Chen F; Zhang Q; Shen Y; Safran M; Lancet D; Fishilevich S BMC Med Genomics; 2019 Dec; 12(1):200. PubMed ID: 31888639 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]