BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 30474849)

  • 1. Identification of Genomic Alterations Through Multilevel DNA Structural Analysis.
    Shultzaberger RK; Dresios J
    Methods Mol Biol; 2019; 1896():191-201. PubMed ID: 30474849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Agnostic detection of genomic alterations by holistic DNA structural interrogation.
    Shultzaberger RK; Abrams RE; Sullivan CJ; Schmitt AD; Thompson TWJ; Dresios J
    PLoS One; 2018; 13(11):e0208054. PubMed ID: 30496256
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ATAC2GRN: optimized ATAC-seq and DNase1-seq pipelines for rapid and accurate genome regulatory network inference.
    Pranzatelli TJF; Michael DG; Chiorini JA
    BMC Genomics; 2018 Jul; 19(1):563. PubMed ID: 30064353
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of Whole Genome Sequencing Data.
    Hübschmann D; Schlesner M
    Methods Mol Biol; 2019; 1956():321-336. PubMed ID: 30779042
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomic Sequence Variation Analysis by Resequencing.
    Martin J; Schackwitz W; Lipzen A
    Methods Mol Biol; 2018; 1775():229-239. PubMed ID: 29876821
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-Scale Analysis of Cell-Specific Regulatory Codes Using Nuclear Enzymes.
    Baek S; Sung MH
    Methods Mol Biol; 2016; 1418():225-40. PubMed ID: 27008018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DEBrowser: interactive differential expression analysis and visualization tool for count data.
    Kucukural A; Yukselen O; Ozata DM; Moore MJ; Garber M
    BMC Genomics; 2019 Jan; 20(1):6. PubMed ID: 30611200
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomics Methods for
    Gilchrist MJ; Cho KWY; Veenstra GJC
    Cold Spring Harb Protoc; 2020 May; 2020(5):097915. PubMed ID: 32123020
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ChIP-seq for the Identification of Functional Elements in the Human Genome.
    Marinov GK
    Methods Mol Biol; 2017; 1543():3-18. PubMed ID: 28349419
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DamID-seq: Genome-wide Mapping of Protein-DNA Interactions by High Throughput Sequencing of Adenine-methylated DNA Fragments.
    Wu F; Olson BG; Yao J
    J Vis Exp; 2016 Jan; (107):e53620. PubMed ID: 26862720
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole Genome Sequence Analysis and Population Genomics of Group A Streptococci.
    Lacey JA; James TB; Tong SYC; Davies MR
    Methods Mol Biol; 2020; 2136():81-111. PubMed ID: 32430815
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variant detection sensitivity and biases in whole genome and exome sequencing.
    Meynert AM; Ansari M; FitzPatrick DR; Taylor MS
    BMC Bioinformatics; 2014 Jul; 15(1):247. PubMed ID: 25038816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide analysis of chromatin accessibility using ATAC-seq.
    Shashikant T; Ettensohn CA
    Methods Cell Biol; 2019; 151():219-235. PubMed ID: 30948010
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human whole genome sequencing in South Africa.
    Glanzmann B; Jooste T; Ghoor S; Gordon R; Mia R; Mao J; Li H; Charls P; Douman C; Kotze MJ; Peeters AV; Loots G; Esser M; Tiemessen CT; Wilkinson RJ; Louw J; Gray G; Warren RM; Möller M; Kinnear C
    Sci Rep; 2021 Jan; 11(1):606. PubMed ID: 33436733
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Software for rapid time dependent ChIP-sequencing analysis (TDCA).
    Myschyshyn M; Farren-Dai M; Chuang TJ; Vocadlo D
    BMC Bioinformatics; 2017 Nov; 18(1):521. PubMed ID: 29178831
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combined Genome and Transcriptome (G&T) Sequencing of Single Cells.
    Bronner IF; Lorenz S
    Methods Mol Biol; 2019; 1979():319-362. PubMed ID: 31028647
    [TBL] [Abstract][Full Text] [Related]  

  • 17. OCRDetector: Accurately Detecting Open Chromatin Regions via Plasma Cell-Free DNA Sequencing Data.
    Wang J; Chen L; Zhang X; Tong Y; Zheng T
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071577
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NGS-QC Generator: A Quality Control System for ChIP-Seq and Related Deep Sequencing-Generated Datasets.
    Mendoza-Parra MA; Saleem MA; Blum M; Cholley PE; Gronemeyer H
    Methods Mol Biol; 2016; 1418():243-65. PubMed ID: 27008019
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Genome Sequencing and Analysis Methods in Chronic Lymphocytic Leukemia.
    Quesada V; Araujo-Voces M; Pérez-Silva JG; Velasco G; López-Otín C
    Methods Mol Biol; 2019; 1881():319-325. PubMed ID: 30350214
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.