229 related articles for article (PubMed ID: 30915546)
1. OPENMENDEL: a cooperative programming project for statistical genetics.
Zhou H; Sinsheimer JS; Bates DM; Chu BB; German CA; Ji SS; Keys KL; Kim J; Ko S; Mosher GD; Papp JC; Sobel EM; Zhai J; Zhou JJ; Lange K
Hum Genet; 2020 Jan; 139(1):61-71. PubMed ID: 30915546
[TBL] [Abstract][Full Text] [Related]
2. Modern simulation utilities for genetic analysis.
Ji SS; German CA; Lange K; Sinsheimer JS; Zhou H; Zhou J; Sobel EM
BMC Bioinformatics; 2021 May; 22(1):228. PubMed ID: 33941078
[TBL] [Abstract][Full Text] [Related]
3. htSNPer1.0: software for haplotype block partition and htSNPs selection.
Ding K; Zhang J; Zhou K; Shen Y; Zhang X
BMC Bioinformatics; 2005 Mar; 6():38. PubMed ID: 15740612
[TBL] [Abstract][Full Text] [Related]
4. Sketching algorithms for genomic data analysis and querying in a secure enclave.
Kockan C; Zhu K; Dokmai N; Karpov N; Kulekci MO; Woodruff DP; Sahinalp SC
Nat Methods; 2020 Mar; 17(3):295-301. PubMed ID: 32132732
[TBL] [Abstract][Full Text] [Related]
5. parSMURF, a high-performance computing tool for the genome-wide detection of pathogenic variants.
Petrini A; Mesiti M; Schubach M; Frasca M; Danis D; Re M; Grossi G; Cappelletti L; Castrignanò T; Robinson PN; Valentini G
Gigascience; 2020 May; 9(5):. PubMed ID: 32444882
[TBL] [Abstract][Full Text] [Related]
6. Molgenis-impute: imputation pipeline in a box.
Kanterakis A; Deelen P; van Dijk F; Byelas H; Dijkstra M; Swertz MA
BMC Res Notes; 2015 Aug; 8():359. PubMed ID: 26286716
[TBL] [Abstract][Full Text] [Related]
7. Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.
Stenger JE; Xu H; Haynes C; Hauser ER; Pericak-Vance M; Goldschmidt-Clermont PJ; Vance JM
BMC Bioinformatics; 2005 Apr; 6():95. PubMed ID: 15826305
[TBL] [Abstract][Full Text] [Related]
8. A phylogenetic method to perform genome-wide association studies in microbes that accounts for population structure and recombination.
Collins C; Didelot X
PLoS Comput Biol; 2018 Feb; 14(2):e1005958. PubMed ID: 29401456
[TBL] [Abstract][Full Text] [Related]
9. Genetic Parallel Programming: design and implementation.
Cheang SM; Leung KS; Lee KH
Evol Comput; 2006; 14(2):129-56. PubMed ID: 16831104
[TBL] [Abstract][Full Text] [Related]
10. A fast boosting-based screening method for large-scale association study in complex traits with genetic heterogeneity.
Wang LY; Fasulo D
Conf Proc IEEE Eng Med Biol Soc; 2006; 2006():5771-4. PubMed ID: 17946332
[TBL] [Abstract][Full Text] [Related]
11. Bio++: a set of C++ libraries for sequence analysis, phylogenetics, molecular evolution and population genetics.
Dutheil J; Gaillard S; Bazin E; Glémin S; Ranwez V; Galtier N; Belkhir K
BMC Bioinformatics; 2006 Apr; 7():188. PubMed ID: 16594991
[TBL] [Abstract][Full Text] [Related]
12. Sushi.R: flexible, quantitative and integrative genomic visualizations for publication-quality multi-panel figures.
Phanstiel DH; Boyle AP; Araya CL; Snyder MP
Bioinformatics; 2014 Oct; 30(19):2808-10. PubMed ID: 24903420
[TBL] [Abstract][Full Text] [Related]
13. R for genome-wide association studies.
Gondro C; Porto-Neto LR; Lee SH
Methods Mol Biol; 2013; 1019():1-17. PubMed ID: 23756885
[TBL] [Abstract][Full Text] [Related]
14. Fast computation for genome-wide association studies using boosted one-step statistics.
Voorman A; Rice K; Lumley T
Bioinformatics; 2012 Jul; 28(14):1818-22. PubMed ID: 22592383
[TBL] [Abstract][Full Text] [Related]
15. SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations.
Zhan X; Liu DJ
Genet Epidemiol; 2015 Dec; 39(8):619-23. PubMed ID: 26394715
[TBL] [Abstract][Full Text] [Related]
16. minimac2: faster genotype imputation.
Fuchsberger C; Abecasis GR; Hinds DA
Bioinformatics; 2015 Mar; 31(5):782-4. PubMed ID: 25338720
[TBL] [Abstract][Full Text] [Related]
17. Orchestrating high-throughput genomic analysis with Bioconductor.
Huber W; Carey VJ; Gentleman R; Anders S; Carlson M; Carvalho BS; Bravo HC; Davis S; Gatto L; Girke T; Gottardo R; Hahne F; Hansen KD; Irizarry RA; Lawrence M; Love MI; MacDonald J; Obenchain V; Oleś AK; Pagès H; Reyes A; Shannon P; Smyth GK; Tenenbaum D; Waldron L; Morgan M
Nat Methods; 2015 Feb; 12(2):115-21. PubMed ID: 25633503
[TBL] [Abstract][Full Text] [Related]
18. RAREMETAL: fast and powerful meta-analysis for rare variants.
Feng S; Liu D; Zhan X; Wing MK; Abecasis GR
Bioinformatics; 2014 Oct; 30(19):2828-9. PubMed ID: 24894501
[TBL] [Abstract][Full Text] [Related]
19. The statistical properties of gene-set analysis.
de Leeuw CA; Neale BM; Heskes T; Posthuma D
Nat Rev Genet; 2016 Apr; 17(6):353-64. PubMed ID: 27070863
[TBL] [Abstract][Full Text] [Related]
20. Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.
Coleman JR; Euesden J; Patel H; Folarin AA; Newhouse S; Breen G
Brief Funct Genomics; 2016 Jul; 15(4):298-304. PubMed ID: 26443613
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
