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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 27565584)

  • 21. Integrative analysis of multiple genomic variables using a hierarchical Bayesian model.
    Schäfer M; Klein HU; Schwender H
    Bioinformatics; 2017 Oct; 33(20):3220-3227. PubMed ID: 28582573
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Mosdepth: quick coverage calculation for genomes and exomes.
    Pedersen BS; Quinlan AR
    Bioinformatics; 2018 Mar; 34(5):867-868. PubMed ID: 29096012
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An integrated approach for analyzing clinical genomic variant data from next-generation sequencing.
    Crowgey EL; Stabley DL; Chen C; Huang H; Robbins KM; Polson SW; Sol-Church K; Wu CH
    J Biomol Tech; 2015 Apr; 26(1):19-28. PubMed ID: 25649353
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes.
    Smith KR; Bromhead CJ; Hildebrand MS; Shearer AE; Lockhart PJ; Najmabadi H; Leventer RJ; McGillivray G; Amor DJ; Smith RJ; Bahlo M
    Genome Biol; 2011 Sep; 12(9):R85. PubMed ID: 21917141
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Rise and Rise of Exome Sequencing.
    Ku CS; Cooper DN; Patrinos GP
    Public Health Genomics; 2016; 19(6):315-324. PubMed ID: 27898412
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An automatic and efficient pipeline for disease gene identification through utilizing family-based sequencing data.
    Song D; Li N; Liao L
    Biomed Mater Eng; 2015; 26 Suppl 1():S1797-803. PubMed ID: 26405949
    [TBL] [Abstract][Full Text] [Related]  

  • 28. VAR-MD: a tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance.
    Sincan M; Simeonov DR; Adams D; Markello TC; Pierson TM; Toro C; Gahl WA; Boerkoel CF
    Hum Mutat; 2012 Apr; 33(4):593-8. PubMed ID: 22290570
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies.
    Wu J; Li Y; Jiang R
    PLoS Genet; 2014 Mar; 10(3):e1004237. PubMed ID: 24651380
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 31. GATB: Genome Assembly & Analysis Tool Box.
    Drezen E; Rizk G; Chikhi R; Deltel C; Lemaitre C; Peterlongo P; Lavenier D
    Bioinformatics; 2014 Oct; 30(20):2959-61. PubMed ID: 24990603
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A practical guide to filtering and prioritizing genetic variants.
    Jalali Sefid Dashti M; Gamieldien J
    Biotechniques; 2017 Jan; 62(1):18-30. PubMed ID: 28118812
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract.
    Jia X; Zhang F; Bai J; Gao L; Zhang X; Sun H; Sun D; Guan R; Sun W; Xu L; Yue Z; Yu Y; Fu S
    BMC Med Genet; 2013 Oct; 14():107. PubMed ID: 24103489
    [TBL] [Abstract][Full Text] [Related]  

  • 34. VIPER: a web application for rapid expert review of variant calls.
    Wöste M; Dugas M
    Bioinformatics; 2018 Jun; 34(11):1928-1929. PubMed ID: 29346510
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Next-generation diagnostics and disease-gene discovery with the Exomiser.
    Smedley D; Jacobsen JO; Jäger M; Köhler S; Holtgrewe M; Schubach M; Siragusa E; Zemojtel T; Buske OJ; Washington NL; Bone WP; Haendel MA; Robinson PN
    Nat Protoc; 2015 Dec; 10(12):2004-15. PubMed ID: 26562621
    [TBL] [Abstract][Full Text] [Related]  

  • 37. ngsCAT: a tool to assess the efficiency of targeted enrichment sequencing.
    López-Domingo FJ; Florido JP; Rueda A; Dopazo J; Santoyo-Lopez J
    Bioinformatics; 2014 Jun; 30(12):1767-8. PubMed ID: 24578402
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Reducing the search space for causal genetic variants with VASP.
    Field MA; Cho V; Cook MC; Enders A; Vinuesa CG; Whittle B; Andrews TD; Goodnow CC
    Bioinformatics; 2015 Jul; 31(14):2377-9. PubMed ID: 25755272
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prioritization Of Nonsynonymous Single Nucleotide Variants For Exome Sequencing Studies Via Integrative Learning On Multiple Genomic Data.
    Wu M; Wu J; Chen T; Jiang R
    Sci Rep; 2015 Oct; 5():14955. PubMed ID: 26459872
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Global inference of disease-causing single nucleotide variants from exome sequencing data.
    Wu M; Chen T; Jiang R
    BMC Bioinformatics; 2016 Dec; 17(Suppl 17):468. PubMed ID: 28155632
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.