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 *

220 related articles for article (PubMed ID: 21144010)

  • 1. Overcoming bias and systematic errors in next generation sequencing data.
    Taub MA; Corrada Bravo H; Irizarry RA
    Genome Med; 2010 Dec; 2(12):87. PubMed ID: 21144010
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detecting and overcoming systematic bias in high-throughput screening technologies: a comprehensive review of practical issues and methodological solutions.
    Caraus I; Alsuwailem AA; Nadon R; Makarenkov V
    Brief Bioinform; 2015 Nov; 16(6):974-86. PubMed ID: 25750417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The future of Cochrane Neonatal.
    Soll RF; Ovelman C; McGuire W
    Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevention, diagnosis and treatment of high-throughput sequencing data pathologies.
    Zhou X; Rokas A
    Mol Ecol; 2014 Apr; 23(7):1679-700. PubMed ID: 24471475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection and removal of biases in the analysis of next-generation sequencing reads.
    Schwartz S; Oren R; Ast G
    PLoS One; 2011 Jan; 6(1):e16685. PubMed ID: 21304912
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identifying and mitigating bias in next-generation sequencing methods for chromatin biology.
    Meyer CA; Liu XS
    Nat Rev Genet; 2014 Nov; 15(11):709-21. PubMed ID: 25223782
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhancement of Plant Productivity in the Post-Genomics Era.
    Thao NP; Tran LS
    Curr Genomics; 2016 Aug; 17(4):295-6. PubMed ID: 27499678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Volume and health outcomes: evidence from systematic reviews and from evaluation of Italian hospital data].
    Amato L; Colais P; Davoli M; Ferroni E; Fusco D; Minozzi S; Moirano F; Sciattella P; Vecchi S; Ventura M; Perucci CA
    Epidemiol Prev; 2013; 37(2-3 Suppl 2):1-100. PubMed ID: 23851286
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Volume and health outcomes: evidence from systematic reviews and from evaluation of Italian hospital data.
    Amato L; Fusco D; Acampora A; Bontempi K; Rosa AC; Colais P; Cruciani F; D'Ovidio M; Mataloni F; Minozzi S; Mitrova Z; Pinnarelli L; Saulle R; Soldati S; Sorge C; Vecchi S; Ventura M; Davoli M
    Epidemiol Prev; 2017; 41(5-6 (Suppl 2)):1-128. PubMed ID: 29205995
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detecting and removing multiplicative spatial bias in high-throughput screening technologies.
    Caraus I; Mazoure B; Nadon R; Makarenkov V
    Bioinformatics; 2017 Oct; 33(20):3258-3267. PubMed ID: 28633418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification and correction of systematic error in high-throughput sequence data.
    Meacham F; Boffelli D; Dhahbi J; Martin DI; Singer M; Pachter L
    BMC Bioinformatics; 2011 Nov; 12():451. PubMed ID: 22099972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Quantifying population genetic differentiation from next-generation sequencing data.
    Fumagalli M; Vieira FG; Korneliussen TS; Linderoth T; Huerta-Sánchez E; Albrechtsen A; Nielsen R
    Genetics; 2013 Nov; 195(3):979-92. PubMed ID: 23979584
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Is it time we get real? A systematic review of the potential of data-driven technologies to address teachers' implicit biases.
    Gauthier A; Rizvi S; Cukurova M; Mavrikis M
    Front Artif Intell; 2022; 5():994967. PubMed ID: 36304958
    [TBL] [Abstract][Full Text] [Related]  

  • 15. From next-generation resequencing reads to a high-quality variant data set.
    Pfeifer SP
    Heredity (Edinb); 2017 Feb; 118(2):111-124. PubMed ID: 27759079
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Understanding and overcoming the pitfalls and biases of next-generation sequencing (NGS) methods for use in the routine clinical microbiological diagnostic laboratory.
    Boers SA; Jansen R; Hays JP
    Eur J Clin Microbiol Infect Dis; 2019 Jun; 38(6):1059-1070. PubMed ID: 30834996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Illumina error profiles: resolving fine-scale variation in metagenomic sequencing data.
    Schirmer M; D'Amore R; Ijaz UZ; Hall N; Quince C
    BMC Bioinformatics; 2016 Mar; 17():125. PubMed ID: 26968756
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deep sequencing of evolving pathogen populations: applications, errors, and bioinformatic solutions.
    McElroy K; Thomas T; Luciani F
    Microb Inform Exp; 2014 Jan; 4(1):1. PubMed ID: 24428920
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-throughput qPCR and 16S rRNA gene amplicon sequencing as complementary methods for the investigation of the cheese microbiota.
    Dreier M; Meola M; Berthoud H; Shani N; Wechsler D; Junier P
    BMC Microbiol; 2022 Feb; 22(1):48. PubMed ID: 35130830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Measurements of Intrahost Viral Diversity Are Extremely Sensitive to Systematic Errors in Variant Calling.
    McCrone JT; Lauring AS
    J Virol; 2016 Aug; 90(15):6884-95. PubMed ID: 27194763
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.