BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 30902345)

  • 21. Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing.
    Sanchis-Juan A; Stephens J; French CE; Gleadall N; Mégy K; Penkett C; Shamardina O; Stirrups K; Delon I; Dewhurst E; Dolling H; Erwood M; Grozeva D; Stefanucci L; Arno G; Webster AR; Cole T; Austin T; Branco RG; Ouwehand WH; Raymond FL; Carss KJ
    Genome Med; 2018 Dec; 10(1):95. PubMed ID: 30526634
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Accurate genotyping across variant classes and lengths using variant graphs.
    Sibbesen JA; Maretty L; ; Krogh A
    Nat Genet; 2018 Jul; 50(7):1054-1059. PubMed ID: 29915429
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Early MinION™ nanopore single-molecule sequencing technology enables the characterization of hepatitis B virus genetic complexity in clinical samples.
    Sauvage V; Boizeau L; Candotti D; Vandenbogaert M; Servant-Delmas A; Caro V; Laperche S
    PLoS One; 2018; 13(3):e0194366. PubMed ID: 29566006
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genome assembly using Nanopore-guided long and error-free DNA reads.
    Madoui MA; Engelen S; Cruaud C; Belser C; Bertrand L; Alberti A; Lemainque A; Wincker P; Aury JM
    BMC Genomics; 2015 Apr; 16(1):327. PubMed ID: 25927464
    [TBL] [Abstract][Full Text] [Related]  

  • 25. COSMOS: accurate detection of somatic structural variations through asymmetric comparison between tumor and normal samples.
    Yamagata K; Yamanishi A; Kokubu C; Takeda J; Sese J
    Nucleic Acids Res; 2016 May; 44(8):e78. PubMed ID: 26833260
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SM-RCNV: a statistical method to detect recurrent copy number variations in sequenced samples.
    Li Y; Yuan X; Zhang J; Yang L; Bai J; Jiang S
    Genes Genomics; 2019 May; 41(5):529-536. PubMed ID: 30779024
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Progress in detecting genetic alterations and their association with human disease.
    Schwartz CE; Chen CF
    J Mol Biol; 2013 Nov; 425(21):3914-8. PubMed ID: 23876707
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Taming the genome: towards better genetic test interpretation.
    Caleshu C; Ashley EA
    Genome Med; 2016 Jun; 8(1):70. PubMed ID: 27324065
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome structural variation discovery and genotyping.
    Alkan C; Coe BP; Eichler EE
    Nat Rev Genet; 2011 May; 12(5):363-76. PubMed ID: 21358748
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. iMGEins: detecting novel mobile genetic elements inserted in individual genomes.
    Bae J; Lee KW; Islam MN; Yim HS; Park H; Rho M
    BMC Genomics; 2018 Dec; 19(1):944. PubMed ID: 30563451
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Improvements in Genomic Technologies: Application to Crop Genomics.
    Yuan Y; Bayer PE; Batley J; Edwards D
    Trends Biotechnol; 2017 Jun; 35(6):547-558. PubMed ID: 28284542
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Opportunities and challenges of whole-genome and -exome sequencing.
    Petersen BS; Fredrich B; Hoeppner MP; Ellinghaus D; Franke A
    BMC Genet; 2017 Feb; 18(1):14. PubMed ID: 28193154
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ultra high throughput sequencing in human DNA variation detection: a comparative study on the NDUFA3-PRPF31 region.
    Benaglio P; Rivolta C
    PLoS One; 2010 Sep; 5(9):. PubMed ID: 20927379
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Coming of age: ten years of next-generation sequencing technologies.
    Goodwin S; McPherson JD; McCombie WR
    Nat Rev Genet; 2016 May; 17(6):333-51. PubMed ID: 27184599
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Toolkit for automated and rapid discovery of structural variants.
    Soylev A; Kockan C; Hormozdiari F; Alkan C
    Methods; 2017 Oct; 129():3-7. PubMed ID: 28583483
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Single-Molecule Sequencing: Towards Clinical Applications.
    Ameur A; Kloosterman WP; Hestand MS
    Trends Biotechnol; 2019 Jan; 37(1):72-85. PubMed ID: 30115375
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Nonoverlapping clone pooling for high-throughput sequencing.
    Kuroshu RM
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(5):1091-7. PubMed ID: 24384700
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Next-generation technologies to determine plastid genome sequences.
    Henry RJ; Rice N; Edwards M; Nock CJ
    Methods Mol Biol; 2014; 1132():39-46. PubMed ID: 24599845
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.