BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 33906263)

  • 21. Detection Copy Number Variants from NGS with Sparse and Smooth Constraints.
    Zhang Y; Cheung YM; Xu B; Su W
    IEEE/ACM Trans Comput Biol Bioinform; 2017; 14(4):856-867. PubMed ID: 27164604
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identifying multi-layer gene regulatory modules from multi-dimensional genomic data.
    Li W; Zhang S; Liu CC; Zhou XJ
    Bioinformatics; 2012 Oct; 28(19):2458-66. PubMed ID: 22863767
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. An integrative characterization of recurrent molecular aberrations in glioblastoma genomes.
    Sintupisut N; Liu PL; Yeang CH
    Nucleic Acids Res; 2013 Oct; 41(19):8803-21. PubMed ID: 23907387
    [TBL] [Abstract][Full Text] [Related]  

  • 25. CNV Radar: an improved method for somatic copy number alteration characterization in oncology.
    Soong D; Stratford J; Avet-Loiseau H; Bahlis N; Davies F; Dispenzieri A; Sasser AK; Schecter JM; Qi M; Brown C; Jones W; Keats JJ; Auclair D; Chiu C; Powers J; Schaffer M
    BMC Bioinformatics; 2020 Mar; 21(1):98. PubMed ID: 32143562
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of copy number variants from exome sequence data.
    Samarakoon PS; Sorte HS; Kristiansen BE; Skodje T; Sheng Y; Tjønnfjord GE; Stadheim B; Stray-Pedersen A; Rødningen OK; Lyle R
    BMC Genomics; 2014 Aug; 15(1):661. PubMed ID: 25102989
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Three-dimensional genome landscape comprehensively reveals patterns of spatial gene regulation in papillary and anaplastic thyroid cancers: a study using representative cell lines for each cancer type.
    Zhang L; Xu M; Zhang W; Zhu C; Cui Z; Fu H; Ma Y; Huang S; Cui J; Liang S; Huang L; Wang H
    Cell Mol Biol Lett; 2023 Jan; 28(1):1. PubMed ID: 36609218
    [TBL] [Abstract][Full Text] [Related]  

  • 29. X-CNV: genome-wide prediction of the pathogenicity of copy number variations.
    Zhang L; Shi J; Ouyang J; Zhang R; Tao Y; Yuan D; Lv C; Wang R; Ning B; Roberts R; Tong W; Liu Z; Shi T
    Genome Med; 2021 Aug; 13(1):132. PubMed ID: 34407882
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A scalable artificial intelligence platform that automatically finds copy number variations (CNVs) in journal articles and transforms them into a database: CNV extraction, transformation, and loading AI (CNV-ETLAI).
    Choi J; Jeon S; Kim D; Chua M; Do S
    Comput Biol Med; 2022 May; 144():105332. PubMed ID: 35240378
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Insights into Impact of DNA Copy Number Alteration and Methylation on the Proteogenomic Landscape of Human Ovarian Cancer via a Multi-omics Integrative Analysis.
    Song X; Ji J; Gleason KJ; Yang F; Martignetti JA; Chen LS; Wang P
    Mol Cell Proteomics; 2019 Aug; 18(8 suppl 1):S52-S65. PubMed ID: 31227599
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of mutated core cancer modules by integrating somatic mutation, copy number variation, and gene expression data.
    Zhang J; Zhang S; Wang Y; Zhang XS
    BMC Syst Biol; 2013; 7 Suppl 2(Suppl 2):S4. PubMed ID: 24565034
    [TBL] [Abstract][Full Text] [Related]  

  • 33. BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN.
    Kim D; Lucas A; Glessner J; Verma SS; Bradford Y; Li R; Frase AT; Hakonarson H; Peissig P; Brilliant M; Ritchie MD
    Pac Symp Biocomput; 2016; 21():357-68. PubMed ID: 26776200
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Estimation of correlations between copy-number variants in non-coding DNA.
    Stamoulis C
    Annu Int Conf IEEE Eng Med Biol Soc; 2011; 2011():5563-6. PubMed ID: 22255599
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inferring gene regulatory relationships with a high-dimensional robust approach.
    Zang Y; Zhao Q; Zhang Q; Li Y; Zhang S; Ma S
    Genet Epidemiol; 2017 Jul; 41(5):437-454. PubMed ID: 28464328
    [TBL] [Abstract][Full Text] [Related]  

  • 36. miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.
    Qiao Y; Badduke C; Mercier E; Lewis SM; Pavlidis P; Rajcan-Separovic E
    BMC Genomics; 2013 Aug; 14():544. PubMed ID: 23937676
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Local Outlier Factor-Based Detection of Copy Number Variations From NGS Data.
    Yuan X; Li J; Bai J; Xi J
    IEEE/ACM Trans Comput Biol Bioinform; 2021; 18(5):1811-1820. PubMed ID: 31880558
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.
    Brucker A; Lu W; Marceau West R; Yu QY; Hsiao CK; Hsiao TH; Lin CH; Magnusson PKE; Sullivan PF; Szatkiewicz JP; Lu TP; Tzeng JY
    PLoS Comput Biol; 2020 May; 16(5):e1007797. PubMed ID: 32365089
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Copy-number variation: the balance between gene dosage and expression in Drosophila melanogaster.
    Zhou J; Lemos B; Dopman EB; Hartl DL
    Genome Biol Evol; 2011; 3():1014-24. PubMed ID: 21979154
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel signal processing approach for the detection of copy number variations in the human genome.
    Stamoulis C; Betensky RA
    Bioinformatics; 2011 Sep; 27(17):2338-45. PubMed ID: 21752800
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.