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 *

224 related articles for article (PubMed ID: 27166244)

  • 21. pIRS: Profile-based Illumina pair-end reads simulator.
    Hu X; Yuan J; Shi Y; Lu J; Liu B; Li Z; Chen Y; Mu D; Zhang H; Li N; Yue Z; Bai F; Li H; Fan W
    Bioinformatics; 2012 Jun; 28(11):1533-5. PubMed ID: 22508794
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clustering of circular consensus sequences: accurate error correction and assembly of single molecule real-time reads from multiplexed amplicon libraries.
    Francis F; Dumas MD; Davis SB; Wisser RJ
    BMC Bioinformatics; 2018 Aug; 19(1):302. PubMed ID: 30126356
    [TBL] [Abstract][Full Text] [Related]  

  • 23. LSCplus: a fast solution for improving long read accuracy by short read alignment.
    Hu R; Sun G; Sun X
    BMC Bioinformatics; 2016 Nov; 17(1):451. PubMed ID: 27829364
    [TBL] [Abstract][Full Text] [Related]  

  • 24. HISEA: HIerarchical SEed Aligner for PacBio data.
    Khiste N; Ilie L
    BMC Bioinformatics; 2017 Dec; 18(1):564. PubMed ID: 29258419
    [TBL] [Abstract][Full Text] [Related]  

  • 25. SMRT sequencing only de novo assembly of the sugar beet (Beta vulgaris) chloroplast genome.
    Stadermann KB; Weisshaar B; Holtgräwe D
    BMC Bioinformatics; 2015 Sep; 16(1):295. PubMed ID: 26377912
    [TBL] [Abstract][Full Text] [Related]  

  • 26. ARCS: scaffolding genome drafts with linked reads.
    Yeo S; Coombe L; Warren RL; Chu J; Birol I
    Bioinformatics; 2018 Mar; 34(5):725-731. PubMed ID: 29069293
    [TBL] [Abstract][Full Text] [Related]  

  • 27. NextGenMap: fast and accurate read mapping in highly polymorphic genomes.
    Sedlazeck FJ; Rescheneder P; von Haeseler A
    Bioinformatics; 2013 Nov; 29(21):2790-1. PubMed ID: 23975764
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Wessim: a whole-exome sequencing simulator based on in silico exome capture.
    Kim S; Jeong K; Bafna V
    Bioinformatics; 2013 Apr; 29(8):1076-7. PubMed ID: 23413434
    [TBL] [Abstract][Full Text] [Related]  

  • 29. RNF: a general framework to evaluate NGS read mappers.
    Břinda K; Boeva V; Kucherov G
    Bioinformatics; 2016 Jan; 32(1):136-9. PubMed ID: 26353839
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Error filtering, pair assembly and error correction for next-generation sequencing reads.
    Edgar RC; Flyvbjerg H
    Bioinformatics; 2015 Nov; 31(21):3476-82. PubMed ID: 26139637
    [TBL] [Abstract][Full Text] [Related]  

  • 31. BleTIES: annotation of natural genome editing in ciliates using long read sequencing.
    Seah BKB; Swart EC
    Bioinformatics; 2021 Nov; 37(21):3929-3931. PubMed ID: 34487139
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FLAS: fast and high-throughput algorithm for PacBio long-read self-correction.
    Bao E; Xie F; Song C; Song D
    Bioinformatics; 2019 Oct; 35(20):3953-3960. PubMed ID: 30895306
    [TBL] [Abstract][Full Text] [Related]  

  • 33. NanoPack: visualizing and processing long-read sequencing data.
    De Coster W; D'Hert S; Schultz DT; Cruts M; Van Broeckhoven C
    Bioinformatics; 2018 Aug; 34(15):2666-2669. PubMed ID: 29547981
    [TBL] [Abstract][Full Text] [Related]  

  • 34. TALC: Transcript-level Aware Long-read Correction.
    Broseus L; Thomas A; Oldfield AJ; Severac D; Dubois E; Ritchie W
    Bioinformatics; 2020 Dec; 36(20):5000-5006. PubMed ID: 32910174
    [TBL] [Abstract][Full Text] [Related]  

  • 35. LAMSA: fast split read alignment with long approximate matches.
    Liu B; Gao Y; Wang Y
    Bioinformatics; 2017 Jan; 33(2):192-201. PubMed ID: 27667793
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Designing robust watermark barcodes for multiplex long-read sequencing.
    Ezpeleta J; Krsticevic FJ; Bulacio P; Tapia E
    Bioinformatics; 2017 Mar; 33(6):807-813. PubMed ID: 27259539
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A5-miseq: an updated pipeline to assemble microbial genomes from Illumina MiSeq data.
    Coil D; Jospin G; Darling AE
    Bioinformatics; 2015 Feb; 31(4):587-9. PubMed ID: 25338718
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MsPAC: a tool for haplotype-phased structural variant detection.
    Rodriguez OL; Ritz A; Sharp AJ; Bashir A
    Bioinformatics; 2020 Feb; 36(3):922-924. PubMed ID: 31397844
    [TBL] [Abstract][Full Text] [Related]  

  • 39. damidseq_pipeline: an automated pipeline for processing DamID sequencing datasets.
    Marshall OJ; Brand AH
    Bioinformatics; 2015 Oct; 31(20):3371-3. PubMed ID: 26112292
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Simulating the dynamics of targeted capture sequencing with CapSim.
    Cao MD; Ganesamoorthy D; Zhou C; Coin LJM
    Bioinformatics; 2018 Mar; 34(5):873-874. PubMed ID: 29092025
    [TBL] [Abstract][Full Text] [Related]  

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