BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

257 related articles for article (PubMed ID: 26458888)

  • 1. Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations.
    Cao S; Qin H; Gossmann A; Deng HW; Wang YP
    Bioinformatics; 2016 Feb; 32(3):330-7. PubMed ID: 26458888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. GWASeq: targeted re-sequencing follow up to GWAS.
    Salomon MP; Li WL; Edlund CK; Morrison J; Fortini BK; Win AK; Conti DV; Thomas DC; Duggan D; Buchanan DD; Jenkins MA; Hopper JL; Gallinger S; Le Marchand L; Newcomb PA; Casey G; Marjoram P
    BMC Genomics; 2016 Mar; 17():176. PubMed ID: 26940994
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improved methods for multi-trait fine mapping of pleiotropic risk loci.
    Kichaev G; Roytman M; Johnson R; Eskin E; Lindström S; Kraft P; Pasaniuc B
    Bioinformatics; 2017 Jan; 33(2):248-255. PubMed ID: 27663501
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A unified sparse representation for sequence variant identification for complex traits.
    Cao S; Qin H; Deng HW; Wang YP
    Genet Epidemiol; 2014 Dec; 38(8):671-9. PubMed ID: 25195875
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Likelihood-based complex trait association testing for arbitrary depth sequencing data.
    Yan S; Yuan S; Xu Z; Zhang B; Zhang B; Kang G; Byrnes A; Li Y
    Bioinformatics; 2015 Sep; 31(18):2955-62. PubMed ID: 25979475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.
    Shringarpure SS; Mathias RA; Hernandez RD; O'Connor TD; Szpiech ZA; Torres R; De La Vega FM; Bustamante CD; Barnes KC; Taub MA;
    Bioinformatics; 2017 Apr; 33(8):1147-1153. PubMed ID: 28035032
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Lasso multi-marker mixed model for association mapping with population structure correction.
    Rakitsch B; Lippert C; Stegle O; Borgwardt K
    Bioinformatics; 2013 Jan; 29(2):206-14. PubMed ID: 23175758
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GLANET: genomic loci annotation and enrichment tool.
    Otlu B; Firtina C; Keles S; Tastan O
    Bioinformatics; 2017 Sep; 33(18):2818-2828. PubMed ID: 28541490
    [TBL] [Abstract][Full Text] [Related]  

  • 9. QTL mapping using high-throughput sequencing.
    Jamann TM; Balint-Kurti PJ; Holland JB
    Methods Mol Biol; 2015; 1284():257-85. PubMed ID: 25757777
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
    Chen R; Wei Q; Zhan X; Zhong X; Sutcliffe JS; Cox NJ; Cook EH; Li C; Chen W; Li B
    Bioinformatics; 2015 May; 31(9):1452-9. PubMed ID: 25568282
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Estimation of QTL heritability based on pooled sequencing data.
    Tang W; Huang L; Bu S; Zhang X; Wu W
    Bioinformatics; 2018 Mar; 34(6):978-984. PubMed ID: 29106443
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Zoom-Focus algorithm (ZFA) to locate the optimal testing region for rare variant association tests.
    Wang MH; Weng H; Sun R; Lee J; Wu WKK; Chong KC; Zee BC
    Bioinformatics; 2017 Aug; 33(15):2330-2336. PubMed ID: 28334355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simulating the dynamics of targeted capture sequencing with CapSim.
    Cao MD; Ganesamoorthy D; Zhou C; Coin LJM
    Bioinformatics; 2018 Mar; 34(5):873-874. PubMed ID: 29092025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromatin accessibility prediction via a hybrid deep convolutional neural network.
    Liu Q; Xia F; Yin Q; Jiang R
    Bioinformatics; 2018 Mar; 34(5):732-738. PubMed ID: 29069282
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A multi-scenario genome-wide medical population genetics simulation framework.
    Mugo JW; Geza E; Defo J; Elsheikh SSM; Mazandu GK; Mulder NJ; Chimusa ER
    Bioinformatics; 2017 Oct; 33(19):2995-3002. PubMed ID: 28957497
    [TBL] [Abstract][Full Text] [Related]  

  • 17. JEPEG: a summary statistics based tool for gene-level joint testing of functional variants.
    Lee D; Williamson VS; Bigdeli TB; Riley BP; Fanous AH; Vladimirov VI; Bacanu SA
    Bioinformatics; 2015 Apr; 31(8):1176-82. PubMed ID: 25505091
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detecting Multiethnic Rare Variants.
    Ouyang W; Zhu X; Qin H
    Methods Mol Biol; 2017; 1666():527-538. PubMed ID: 28980263
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A coordinate descent approach for sparse Bayesian learning in high dimensional QTL mapping and genome-wide association studies.
    Wang M; Xu S
    Bioinformatics; 2019 Nov; 35(21):4327-4335. PubMed ID: 31081037
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DeepPerVar: a multi-modal deep learning framework for functional interpretation of genetic variants in personal genome.
    Wang Y; Chen L
    Bioinformatics; 2022 Dec; 38(24):5340-5351. PubMed ID: 36271868
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.