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 *

60 related articles for article (PubMed ID: 25742008)

  • 21. The Cardio-Pad
    Noubiap JJ; Kamtchum-Tatuene J; Nganou-Gnindjio CN; Jingi AM
    Cardiovasc Diagn Ther; 2017 Feb; 7(1):98-101. PubMed ID: 28164018
    [No Abstract]   [Full Text] [Related]  

  • 22. Cardio Vascular Disease Monitoring and Therapy.
    Indian J Nephrol; 2020 Jul; 30(Suppl 1):S67. PubMed ID: 33149391
    [No Abstract]   [Full Text] [Related]  

  • 23. Some recent papers on Cardio-Vascular Conditions.
    Can Med Assoc J; 1911 Jan; 1(1):83-8. PubMed ID: 20310104
    [No Abstract]   [Full Text] [Related]  

  • 24. On variations in the activity of the cardio-inhibitory centre.
    McDowall RJ
    J Physiol; 1931 Apr; 71(4):417-30. PubMed ID: 16994191
    [No Abstract]   [Full Text] [Related]  

  • 25. LocusTrack: Integrated visualization of GWAS results and genomic annotation.
    Cuellar-Partida G; Renteria ME; MacGregor S
    Source Code Biol Med; 2015; 10():1. PubMed ID: 25750659
    [TBL] [Abstract][Full Text] [Related]  

  • 26. From Gigabyte to Kilobyte: A Bioinformatics Protocol for Mining Large RNA-Seq Transcriptomics Data.
    Li J; Hou J; Sun L; Wilkins JM; Lu Y; Niederhuth CE; Merideth BR; Mawhinney TP; Mossine VV; Greenlief CM; Walker JC; Folk WR; Hannink M; Lubahn DB; Birchler JA; Cheng J
    PLoS One; 2015; 10(4):e0125000. PubMed ID: 25902288
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
    Nead KT; Li A; Wehner MR; Neupane B; Gustafsson S; Butterworth A; Engert JC; Davis AD; Hegele RA; Miller R; den Hoed M; Khaw KT; Kilpeläinen TO; Wareham N; Edwards TL; Hallmans G; Varga TV; Kardia SL; Smith JA; Zhao W; Faul JD; Weir D; Mi J; Xi B; Quinteros SC; Cooper C; Sayer AA; Jameson K; Grøntved A; Fornage M; Sidney S; Hanis CL; Highland HM; Häring HU; Heni M; Lasky-Su J; Weiss ST; Gerhard GS; Still C; Melka MM; Pausova Z; Paus T; Grant SF; Hakonarson H; Price RA; Wang K; Scherag A; Hebebrand J; Hinney A; ; Franks PW; Frayling TM; McCarthy MI; Hirschhorn JN; Loos RJ; Ingelsson E; Gerstein HC; Yusuf S; Beyene J; Anand SS; Meyre D
    Hum Mol Genet; 2015 Jun; 24(12):3582-94. PubMed ID: 25784503
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole-genome sequencing for comparative genomics and de novo genome assembly.
    Benjak A; Sala C; Hartkoorn RC
    Methods Mol Biol; 2015; 1285():1-16. PubMed ID: 25779307
    [TBL] [Abstract][Full Text] [Related]  

  • 29. edgeRun: an R package for sensitive, functionally relevant differential expression discovery using an unconditional exact test.
    Dimont E; Shi J; Kirchner R; Hide W
    Bioinformatics; 2015 Aug; 31(15):2589-90. PubMed ID: 25900919
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Babelomics 5.0: functional interpretation for new generations of genomic data.
    Alonso R; Salavert F; Garcia-Garcia F; Carbonell-Caballero J; Bleda M; Garcia-Alonso L; Sanchis-Juan A; Perez-Gil D; Marin-Garcia P; Sanchez R; Cubuk C; Hidalgo MR; Amadoz A; Hernansaiz-Ballesteros RD; Alemán A; Tarraga J; Montaner D; Medina I; Dopazo J
    Nucleic Acids Res; 2015 Jul; 43(W1):W117-21. PubMed ID: 25897133
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Re-alignment of the unmapped reads with base quality score.
    Peng X; Wang J; Zhang Z; Xiao Q; Li M; Pan Y
    BMC Bioinformatics; 2015; 16 Suppl 5(Suppl 5):S8. PubMed ID: 25860434
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Influence of depression on genetic predisposition to type 2 diabetes in a multiethnic longitudinal study.
    Garasia S; Samaan Z; Gerstein HC; Engert JC; Mohan V; Diaz R; Anand SS; Meyre D
    Sci Rep; 2017 May; 7(1):1629. PubMed ID: 28487510
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study.
    Christie S; Robiou-du-Pont S; Anand SS; Morrison KM; McDonald SD; Paré G; Atkinson SA; Teo KK; Meyre D
    Sci Rep; 2017 Mar; 7(1):68. PubMed ID: 28250428
    [TBL] [Abstract][Full Text] [Related]  

  • 34. From big data analysis to personalized medicine for all: challenges and opportunities.
    Alyass A; Turcotte M; Meyre D
    BMC Med Genomics; 2015 Jun; 8():33. PubMed ID: 26112054
    [TBL] [Abstract][Full Text] [Related]  

  • 35. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.
    Johnson AD; Handsaker RE; Pulit SL; Nizzari MM; O'Donnell CJ; de Bakker PI
    Bioinformatics; 2008 Dec; 24(24):2938-9. PubMed ID: 18974171
    [TBL] [Abstract][Full Text] [Related]  

  • 36. SNPdetector: a software tool for sensitive and accurate SNP detection.
    Zhang J; Wheeler DA; Yakub I; Wei S; Sood R; Rowe W; Liu PP; Gibbs RA; Buetow KH
    PLoS Comput Biol; 2005 Oct; 1(5):e53. PubMed ID: 16261194
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Effect of genome-wide genotyping and reference panels on rare variants imputation.
    Zheng HF; Ladouceur M; Greenwood CM; Richards JB
    J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Current bioinformatics tools in genomic biomedical research (Review).
    Teufel A; Krupp M; Weinmann A; Galle PR
    Int J Mol Med; 2006 Jun; 17(6):967-73. PubMed ID: 16685403
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Should we have blind faith in bioinformatics software? Illustrations from the SNAP web-based tool.
    Robiou-du-Pont S; Li A; Christie S; Sohani ZN; Meyre D
    PLoS One; 2015; 10(3):e0118925. PubMed ID: 25742008
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.