BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 29990238)

  • 1. Detecting Population-Differentiation Copy Number Variants in Human Population Tree by Sparse Group Selection.
    Zhang H; Roe D; Kuang R
    IEEE/ACM Trans Comput Biol Bioinform; 2019; 16(2):538-549. PubMed ID: 29990238
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
    Veerappa AM; Suresh RV; Vishweswaraiah S; Lingaiah K; Murthy M; Manjegowda DS; Padakannaya P; Ramachandra NB
    Genet Res (Camb); 2015 Sep; 97():e18. PubMed ID: 26390810
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. A Sparse Learning Framework for Joint Effect Analysis of Copy Number Variants.
    Wang Z; Hall B; Xu J; Shi X
    IEEE/ACM Trans Comput Biol Bioinform; 2017; 14(5):1013-1027. PubMed ID: 28991724
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. CNV_IFTV: An Isolation Forest and Total Variation-Based Detection of CNVs from Short-Read Sequencing Data.
    Yuan X; Yu J; Xi J; Yang L; Shang J; Li Z; Duan J
    IEEE/ACM Trans Comput Biol Bioinform; 2021; 18(2):539-549. PubMed ID: 31180897
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data.
    Zhang Z; Cheng H; Hong X; Di Narzo AF; Franzen O; Peng S; Ruusalepp A; Kovacic JC; Bjorkegren JLM; Wang X; Hao K
    Nucleic Acids Res; 2019 Apr; 47(7):e39. PubMed ID: 30722045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of copy number variation hotspots in human populations.
    Fu W; Zhang F; Wang Y; Gu X; Jin L
    Am J Hum Genet; 2010 Oct; 87(4):494-504. PubMed ID: 20920665
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Haplotype phasing and inheritance of copy number variants in nuclear families.
    Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M
    PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A map of copy number variations in Chinese populations.
    Lou H; Li S; Yang Y; Kang L; Zhang X; Jin W; Wu B; Jin L; Xu S
    PLoS One; 2011; 6(11):e27341. PubMed ID: 22087296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing.
    Onsongo G; Baughn LB; Bower M; Henzler C; Schomaker M; Silverstein KA; Thyagarajan B
    J Mol Diagn; 2016 Nov; 18(6):872-881. PubMed ID: 27597741
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Population-wide copy number variation calling using variant call format files from 6,898 individuals.
    Png G; Suveges D; Park YC; Walter K; Kundu K; Ntalla I; Tsafantakis E; Karaleftheri M; Dedoussis G; Zeggini E; Gilly A
    Genet Epidemiol; 2020 Jan; 44(1):79-89. PubMed ID: 31520489
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CNVcaller: highly efficient and widely applicable software for detecting copy number variations in large populations.
    Wang X; Zheng Z; Cai Y; Chen T; Li C; Fu W; Jiang Y
    Gigascience; 2017 Dec; 6(12):1-12. PubMed ID: 29220491
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variation in Thai population.
    Suktitipat B; Naktang C; Mhuantong W; Tularak T; Artiwet P; Pasomsap E; Jongjaroenprasert W; Fuchareon S; Mahasirimongkol S; Chantratita W; Yimwadsana B; Charoensawan V; Jinawath N
    PLoS One; 2014; 9(8):e104355. PubMed ID: 25118596
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
    da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
    BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history.
    Gaunt TR; Rodriguez S; Guthrie PA; Day IN
    Hum Mutat; 2010 Apr; 31(4):414-20. PubMed ID: 20077501
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.