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 *

116 related articles for article (PubMed ID: 22255943)

  • 1. A pipeline for copy number variation detection based on principal component analysis.
    Chen J; Liu J; Boutte D; Calhoun VD
    Annu Int Conf IEEE Eng Med Biol Soc; 2011; 2011():6975-8. PubMed ID: 22255943
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Correction of Copy Number Variation Data Using Principal Component Analysis.
    Chen J; Liu J; Calhoun VD
    IEEE Int Conf Bioinform Biomed Workshops; 2010 Dec; 2010():827-828. PubMed ID: 30714045
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
    Valsesia A; Stevenson BJ; Waterworth D; Mooser V; Vollenweider P; Waeber G; Jongeneel CV; Beckmann JS; Kutalik Z; Bergmann S
    BMC Genomics; 2012 Jun; 13():241. PubMed ID: 22702538
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. The effect of algorithms on copy number variant detection.
    Tsuang DW; Millard SP; Ely B; Chi P; Wang K; Raskind WH; Kim S; Brkanac Z; Yu CE
    PLoS One; 2010 Dec; 5(12):e14456. PubMed ID: 21209939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Accuracy of CNV Detection from GWAS Data.
    Zhang D; Qian Y; Akula N; Alliey-Rodriguez N; Tang J; ; Gershon ES; Liu C
    PLoS One; 2011 Jan; 6(1):e14511. PubMed ID: 21249187
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inferring combined CNV/SNP haplotypes from genotype data.
    Su SY; Asher JE; Jarvelin MR; Froguel P; Blakemore AI; Balding DJ; Coin LJ
    Bioinformatics; 2010 Jun; 26(11):1437-45. PubMed ID: 20406911
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
    Eckel-Passow JE; Atkinson EJ; Maharjan S; Kardia SL; de Andrade M
    BMC Bioinformatics; 2011 May; 12():220. PubMed ID: 21627824
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Shape-based retrieval of CNV regions in read coverage data.
    Hong S; Yoon J; Hong D; Lee U; Kim B; Park S
    Int J Data Min Bioinform; 2014; 9(3):254-76. PubMed ID: 25163168
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle.
    Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP
    BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assessing the reproducibility of exome copy number variations predictions.
    Hong CS; Singh LN; Mullikin JC; Biesecker LG
    Genome Med; 2016 Aug; 8(1):82. PubMed ID: 27503473
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fast detection of de novo copy number variants from SNP arrays for case-parent trios.
    Scharpf RB; Beaty TH; Schwender H; Younkin SG; Scott AF; Ruczinski I
    BMC Bioinformatics; 2012 Dec; 13():330. PubMed ID: 23234608
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of copy number variation using SNP genotyping.
    Cooper GM; Mefford HC
    Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
    Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
    PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
    Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
    BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnostic implications of genetic copy number variation in epilepsy plus.
    Coppola A; Cellini E; Stamberger H; Saarentaus E; Cetica V; Lal D; Djémié T; Bartnik-Glaska M; Ceulemans B; Helen Cross J; Deconinck T; Masi S; Dorn T; Guerrini R; Hoffman-Zacharska D; Kooy F; Lagae L; Lench N; Lemke JR; Lucenteforte E; Madia F; Mefford HC; Morrogh D; Nuernberg P; Palotie A; Schoonjans AS; Striano P; Szczepanik E; Tostevin A; Vermeesch JR; Van Esch H; Van Paesschen W; Waters JJ; Weckhuysen S; Zara F; De Jonghe P; Sisodiya SM; Marini C; ;
    Epilepsia; 2019 Apr; 60(4):689-706. PubMed ID: 30866059
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.