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 *

238 related articles for article (PubMed ID: 30561546)

  • 41. ReliableGenome: annotation of genomic regions with high/low variant calling concordance.
    Popitsch N; ; Schuh A; Taylor JC
    Bioinformatics; 2017 Jan; 33(2):155-160. PubMed ID: 27605105
    [TBL] [Abstract][Full Text] [Related]  

  • 42. BRISK--research-oriented storage kit for biology-related data.
    Tan A; Tripp B; Daley D
    Bioinformatics; 2011 Sep; 27(17):2422-5. PubMed ID: 21712248
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Efficient querying of genomic reference databases with gget.
    Luebbert L; Pachter L
    Bioinformatics; 2023 Jan; 39(1):. PubMed ID: 36610989
    [TBL] [Abstract][Full Text] [Related]  

  • 44. WhopGenome: high-speed access to whole-genome variation and sequence data in R.
    Wittelsbürger U; Pfeifer B; Lercher MJ
    Bioinformatics; 2015 Feb; 31(3):413-5. PubMed ID: 25273104
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 3Cnet: pathogenicity prediction of human variants using multitask learning with evolutionary constraints.
    Won DG; Kim DW; Woo J; Lee K
    Bioinformatics; 2021 Dec; 37(24):4626-4634. PubMed ID: 34270679
    [TBL] [Abstract][Full Text] [Related]  

  • 46. DrivR-Base: a feature extraction toolkit for variant effect prediction model construction.
    Francis A; Campbell C; Gaunt TR
    Bioinformatics; 2024 Mar; 40(4):. PubMed ID: 38603611
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database.
    Pérez-Palma E; Gramm M; Nürnberg P; May P; Lal D
    Nucleic Acids Res; 2019 Jul; 47(W1):W99-W105. PubMed ID: 31114901
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Var2GO: a web-based tool for gene variants selection.
    Granata I; Sangiovanni M; Maiorano F; Miele M; Guarracino MR
    BMC Bioinformatics; 2016 Nov; 17(Suppl 12):376. PubMed ID: 28185576
    [TBL] [Abstract][Full Text] [Related]  

  • 49. PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions.
    Bendl J; Musil M; Štourač J; Zendulka J; Damborský J; Brezovský J
    PLoS Comput Biol; 2016 May; 12(5):e1004962. PubMed ID: 27224906
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Seshat: A Web service for accurate annotation, validation, and analysis of TP53 variants generated by conventional and next-generation sequencing.
    Tikkanen T; Leroy B; Fournier JL; Risques RA; Malcikova J; Soussi T
    Hum Mutat; 2018 Jul; 39(7):925-933. PubMed ID: 29696732
    [TBL] [Abstract][Full Text] [Related]  

  • 51. wKinMut-2: Identification and Interpretation of Pathogenic Variants in Human Protein Kinases.
    Vazquez M; Pons T; Brunak S; Valencia A; Izarzugaza JM
    Hum Mutat; 2016 Jan; 37(1):36-42. PubMed ID: 26443060
    [TBL] [Abstract][Full Text] [Related]  

  • 52. GSDS 2.0: an upgraded gene feature visualization server.
    Hu B; Jin J; Guo AY; Zhang H; Luo J; Gao G
    Bioinformatics; 2015 Apr; 31(8):1296-7. PubMed ID: 25504850
    [TBL] [Abstract][Full Text] [Related]  

  • 53. AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.
    Makarov V; O'Grady T; Cai G; Lihm J; Buxbaum JD; Yoon S
    Bioinformatics; 2012 Mar; 28(5):724-5. PubMed ID: 22257670
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data.
    Pontikos N; Yu J; Moghul I; Withington L; Blanco-Kelly F; Vulliamy T; Wong TLE; Murphy C; Cipriani V; Fiorentino A; Arno G; Greene D; Jacobsen JOB; Clark T; Gregory DS; Nemeth AM; Halford S; Inglehearn CF; Downes S; Black GC; Webster AR; Hardcastle AJ; ; Plagnol V
    Bioinformatics; 2017 Aug; 33(15):2421-2423. PubMed ID: 28334266
    [TBL] [Abstract][Full Text] [Related]  

  • 55. AnnotSV: an integrated tool for structural variations annotation.
    Geoffroy V; Herenger Y; Kress A; Stoetzel C; Piton A; Dollfus H; Muller J
    Bioinformatics; 2018 Oct; 34(20):3572-3574. PubMed ID: 29669011
    [TBL] [Abstract][Full Text] [Related]  

  • 56. MAVIS: merging, annotation, validation, and illustration of structural variants.
    Reisle C; Mungall KL; Choo C; Paulino D; Bleile DW; Muhammadzadeh A; Mungall AJ; Moore RA; Shlafman I; Coope R; Pleasance S; Ma Y; Jones SJM
    Bioinformatics; 2019 Feb; 35(3):515-517. PubMed ID: 30016509
    [TBL] [Abstract][Full Text] [Related]  

  • 57. ESAP plus: a web-based server for EST-SSR marker development.
    Ponyared P; Ponsawat J; Tongsima S; Seresangtakul P; Akkasaeng C; Tantisuwichwong N
    BMC Genomics; 2016 Dec; 17(Suppl 13):1035. PubMed ID: 28155670
    [TBL] [Abstract][Full Text] [Related]  

  • 58. PROVEAN web server: a tool to predict the functional effect of amino acid substitutions and indels.
    Choi Y; Chan AP
    Bioinformatics; 2015 Aug; 31(16):2745-7. PubMed ID: 25851949
    [TBL] [Abstract][Full Text] [Related]  

  • 59. DaMold: A data-mining platform for variant annotation and visualization in molecular diagnostics research.
    Pandey RV; Pabinger S; Kriegner A; Weinhäusel A
    Hum Mutat; 2017 Jul; 38(7):778-787. PubMed ID: 28397319
    [TBL] [Abstract][Full Text] [Related]  

  • 60. MILANO--custom annotation of microarray results using automatic literature searches.
    Rubinstein R; Simon I
    BMC Bioinformatics; 2005 Jan; 6():12. PubMed ID: 15661078
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.