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 *

216 related articles for article (PubMed ID: 32805016)

  • 1. Integrating genomic correlation structure improves copy number variations detection.
    Luo X; Qin F; Cai G; Xiao F
    Bioinformatics; 2021 Apr; 37(3):312-317. PubMed ID: 32805016
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shall genomic correlation structure be considered in copy number variants detection?
    Qin F; Luo X; Cai G; Xiao F
    Brief Bioinform; 2021 Nov; 22(6):. PubMed ID: 34114005
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Noise cancellation using total variation for copy number variation detection.
    Zare F; Hosny A; Nabavi S
    BMC Bioinformatics; 2018 Oct; 19(Suppl 11):361. PubMed ID: 30343665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modified screening and ranking algorithm for copy number variation detection.
    Xiao F; Min X; Zhang H
    Bioinformatics; 2015 May; 31(9):1341-8. PubMed ID: 25542927
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An accurate and powerful method for copy number variation detection.
    Xiao F; Luo X; Hao N; Niu YS; Xiao X; Cai G; Amos CI; Zhang H
    Bioinformatics; 2019 Sep; 35(17):2891-2898. PubMed ID: 30649252
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide algorithm for detecting CNV associations with diseases.
    Xu Y; Peng B; Fu Y; Amos CI
    BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Integrative DNA copy number detection and genotyping from sequencing and array-based platforms.
    Zhou Z; Wang W; Wang LS; Zhang NR
    Bioinformatics; 2018 Jul; 34(14):2349-2355. PubMed ID: 29992253
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH data.
    Park C; Ahn J; Yoon Y; Park S
    PLoS One; 2011; 6(10):e26975. PubMed ID: 22073121
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number variations in the genome of the Qatari population.
    Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
    BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Modeling genetic inheritance of copy number variations.
    Wang K; Chen Z; Tadesse MG; Glessner J; Grant SF; Hakonarson H; Bucan M; Li M
    Nucleic Acids Res; 2008 Dec; 36(21):e138. PubMed ID: 18832372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.
    Gai X; Perin JC; Murphy K; O'Hara R; D'arcy M; Wenocur A; Xie HM; Rappaport EF; Shaikh TH; White PS
    BMC Bioinformatics; 2010 Feb; 11():74. PubMed ID: 20132550
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CNV-BAC: Copy number Variation Detection in Bacterial Circular Genome.
    Wu L; Wang H; Xia Y; Xi R
    Bioinformatics; 2020 Jun; 36(12):3890-3891. PubMed ID: 32219377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A remark on copy number variation detection methods.
    Li S; Dou X; Gao R; Ge X; Qian M; Wan L
    PLoS One; 2018; 13(4):e0196226. PubMed ID: 29702671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
    Haraksingh RR; Abyzov A; Urban AE
    BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.
    Wong G; Leckie C; Gorringe KL; Haviv I; Campbell IG; Kowalczyk A
    Bioinformatics; 2010 Apr; 26(8):1007-14. PubMed ID: 20189937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data.
    Sinha R; Samaddar S; De RK
    PLoS One; 2015; 10(8):e0135895. PubMed ID: 26291322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genomic predictions combining SNP markers and copy number variations in Nellore cattle.
    Hay EHA; Utsunomiya YT; Xu L; Zhou Y; Neves HHR; Carvalheiro R; Bickhart DM; Ma L; Garcia JF; Liu GE
    BMC Genomics; 2018 Jun; 19(1):441. PubMed ID: 29871610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Population-genetic nature of copy number variations in the human genome.
    Kato M; Kawaguchi T; Ishikawa S; Umeda T; Nakamichi R; Shapero MH; Jones KW; Nakamura Y; Aburatani H; Tsunoda T
    Hum Mol Genet; 2010 Mar; 19(5):761-73. PubMed ID: 19966329
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MONTAGE: a new tool for high-throughput detection of mosaic copy number variation.
    Glessner JT; Chang X; Liu Y; Li J; Khan M; Wei Z; Sleiman PMA; Hakonarson H
    BMC Genomics; 2021 Feb; 22(1):133. PubMed ID: 33627065
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Family-Based Benchmarking of Copy Number Variation Detection Software.
    Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
    PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.