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 *

233 related articles for article (PubMed ID: 22544707)

  • 1. SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).
    Dayem Ullah AZ; Lemoine NR; Chelala C
    Nucleic Acids Res; 2012 Jul; 40(Web Server issue):W65-70. PubMed ID: 22544707
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A practical guide for the functional annotation of genetic variations using SNPnexus.
    Dayem Ullah AZ; Lemoine NR; Chelala C
    Brief Bioinform; 2013 Jul; 14(4):437-47. PubMed ID: 23395730
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.
    Chelala C; Khan A; Lemoine NR
    Bioinformatics; 2009 Mar; 25(5):655-61. PubMed ID: 19098027
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.
    Dayem Ullah AZ; Oscanoa J; Wang J; Nagano A; Lemoine NR; Chelala C
    Nucleic Acids Res; 2018 Jul; 46(W1):W109-W113. PubMed ID: 29757393
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SNPnexus: a web server for functional annotation of human genome sequence variation (2020 update).
    Oscanoa J; Sivapalan L; Gadaleta E; Dayem Ullah AZ; Lemoine NR; Chelala C
    Nucleic Acids Res; 2020 Jul; 48(W1):W185-W192. PubMed ID: 32496546
    [TBL] [Abstract][Full Text] [Related]  

  • 6. VARAdb: a comprehensive variation annotation database for human.
    Pan Q; Liu YJ; Bai XF; Han XL; Jiang Y; Ai B; Shi SS; Wang F; Xu MC; Wang YZ; Zhao J; Chen JX; Zhang J; Li XC; Zhu J; Zhang GR; Wang QY; Li CQ
    Nucleic Acids Res; 2021 Jan; 49(D1):D1431-D1444. PubMed ID: 33095866
    [TBL] [Abstract][Full Text] [Related]  

  • 7. WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation.
    Capriotti E; Calabrese R; Fariselli P; Martelli PL; Altman RB; Casadio R
    BMC Genomics; 2013; 14 Suppl 3(Suppl 3):S6. PubMed ID: 23819482
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transcript annotation tool (TransAT): an R package for retrieving annotations for transcript-specific genetic variants.
    Shih CY; Chattopadhyay A; Wu CH; Tien YW; Lu TP
    BMC Bioinformatics; 2021 Jun; 22(1):350. PubMed ID: 34182919
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
    Huang D; Zhou Y; Yi X; Fan X; Wang J; Yao H; Sham PC; Hao J; Chen K; Li MJ
    Nucleic Acids Res; 2022 Jan; 50(D1):D1408-D1416. PubMed ID: 34570217
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CNVannotator: a comprehensive annotation server for copy number variation in the human genome.
    Zhao M; Zhao Z
    PLoS One; 2013; 8(11):e80170. PubMed ID: 24244640
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SNPsnap: a Web-based tool for identification and annotation of matched SNPs.
    Pers TH; Timshel P; Hirschhorn JN
    Bioinformatics; 2015 Feb; 31(3):418-20. PubMed ID: 25316677
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Snat: a SNP annotation tool for bovine by integrating various sources of genomic information.
    Jiang J; Jiang L; Zhou B; Fu W; Liu JF; Zhang Q
    BMC Genet; 2011 Oct; 12():85. PubMed ID: 21982513
    [TBL] [Abstract][Full Text] [Related]  

  • 14. AVIA v2.0: annotation, visualization and impact analysis of genomic variants and genes.
    Vuong H; Che A; Ravichandran S; Luke BT; Collins JR; Mudunuri US
    Bioinformatics; 2015 Aug; 31(16):2748-50. PubMed ID: 25861966
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Current trend of annotating single nucleotide variation in humans--A case study on SNVrap.
    Li MJ; Wang J
    Methods; 2015 Jun; 79-80():32-40. PubMed ID: 25308971
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DOGMA: a web server for proteome and transcriptome quality assessment.
    Kemena C; Dohmen E; Bornberg-Bauer E
    Nucleic Acids Res; 2019 Jul; 47(W1):W507-W510. PubMed ID: 31076763
    [TBL] [Abstract][Full Text] [Related]  

  • 18. wANNOVAR: annotating genetic variants for personal genomes via the web.
    Chang X; Wang K
    J Med Genet; 2012 Jul; 49(7):433-6. PubMed ID: 22717648
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mercator: a fast and simple web server for genome scale functional annotation of plant sequence data.
    Lohse M; Nagel A; Herter T; May P; Schroda M; Zrenner R; Tohge T; Fernie AR; Stitt M; Usadel B
    Plant Cell Environ; 2014 May; 37(5):1250-8. PubMed ID: 24237261
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.