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 *

169 related articles for article (PubMed ID: 30649252)

  • 41. CNVRuler: a copy number variation-based case-control association analysis tool.
    Kim JH; Hu HJ; Yim SH; Bae JS; Kim SY; Chung YJ
    Bioinformatics; 2012 Jul; 28(13):1790-2. PubMed ID: 22539667
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny.
    Urrutia E; Chen H; Zhou Z; Zhang NR; Jiang Y
    Bioinformatics; 2018 Jun; 34(12):2126-2128. PubMed ID: 29415173
    [TBL] [Abstract][Full Text] [Related]  

  • 43. PEcnv: accurate and efficient detection of copy number variations of various lengths.
    Wang X; Xu Y; Liu R; Lai X; Liu Y; Wang S; Zhang X; Wang J
    Brief Bioinform; 2022 Sep; 23(5):. PubMed ID: 36056740
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Identification of copy number variation in French dairy and beef breeds using next-generation sequencing.
    Letaief R; Rebours E; Grohs C; Meersseman C; Fritz S; Trouilh L; Esquerré D; Barbieri J; Klopp C; Philippe R; Blanquet V; Boichard D; Rocha D; Boussaha M
    Genet Sel Evol; 2017 Oct; 49(1):77. PubMed ID: 29065859
    [TBL] [Abstract][Full Text] [Related]  

  • 45. varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data.
    Kumar AA; Loeys B; Van De Beek G; Peeters N; Wuyts W; Van Laer L; Vandeweyer G; Alaerts M
    Bioinformatics; 2023 Jan; 39(1):. PubMed ID: 36440912
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detection and assessment of copy number variation using PacBio long-read and Illumina sequencing in New Zealand dairy cattle.
    Couldrey C; Keehan M; Johnson T; Tiplady K; Winkelman A; Littlejohn MD; Scott A; Kemper KE; Hayes B; Davis SR; Spelman RJ
    J Dairy Sci; 2017 Jul; 100(7):5472-5478. PubMed ID: 28456410
    [TBL] [Abstract][Full Text] [Related]  

  • 47. An integrative segmentation method for detecting germline copy number variations in SNP arrays.
    Shi J; Li P
    Genet Epidemiol; 2012 May; 36(4):373-83. PubMed ID: 22539397
    [TBL] [Abstract][Full Text] [Related]  

  • 48. CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online.
    Macnee M; Pérez-Palma E; Brünger T; Klöckner C; Platzer K; Stefanski A; Montanucci L; Bayat A; Radtke M; Collins RL; Talkowski M; Blankenberg D; Møller RS; Lemke JR; Nothnagel M; May P; Lal D
    Bioinformatics; 2023 May; 39(5):. PubMed ID: 37104749
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. LLR: a latent low-rank approach to colocalizing genetic risk variants in multiple GWAS.
    Liu J; Wan X; Wang C; Yang C; Zhou X; Yang C
    Bioinformatics; 2017 Dec; 33(24):3878-3886. PubMed ID: 28961754
    [TBL] [Abstract][Full Text] [Related]  

  • 51. cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data.
    Bellos E; Coin LJ
    Bioinformatics; 2014 Sep; 30(17):i639-45. PubMed ID: 25161258
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Combinatorial approach to estimate copy number genotype using whole-exome sequencing data.
    Hwang MY; Moon S; Heo L; Kim YJ; Oh JH; Kim YJ; Kim YK; Lee J; Han BG; Kim BJ
    Genomics; 2015 Mar; 105(3):145-9. PubMed ID: 25535679
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.
    Sapkota Y; Narasimhan A; Kumaran M; Sehrawat BS; Damaraju S
    Cytogenet Genome Res; 2016; 149(3):156-164. PubMed ID: 27668787
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Copy number variation genotyping using family information.
    Chu JH; Rogers A; Ionita-Laza I; Darvishi K; Mills RE; Lee C; Raby BA
    BMC Bioinformatics; 2013 May; 14():157. PubMed ID: 23656838
    [TBL] [Abstract][Full Text] [Related]  

  • 55. An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.
    Zare F; Dow M; Monteleone N; Hosny A; Nabavi S
    BMC Bioinformatics; 2017 May; 18(1):286. PubMed ID: 28569140
    [TBL] [Abstract][Full Text] [Related]  

  • 56. DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism.
    Aguiar D; Halldórsson BV; Morrow EM; Istrail S
    Bioinformatics; 2012 Jun; 28(12):i154-62. PubMed ID: 22689755
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization.
    Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H
    Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374
    [TBL] [Abstract][Full Text] [Related]  

  • 58. CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data.
    Packer JS; Maxwell EK; O'Dushlaine C; Lopez AE; Dewey FE; Chernomorsky R; Baras A; Overton JD; Habegger L; Reid JG
    Bioinformatics; 2016 Jan; 32(1):133-5. PubMed ID: 26382196
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Performance assessment of copy number microarray platforms using a spike-in experiment.
    Halper-Stromberg E; Frelin L; Ruczinski I; Scharpf R; Jie C; Carvalho B; Hao H; Hetrick K; Jedlicka A; Dziedzic A; Doheny K; Scott AF; Baylin S; Pevsner J; Spencer F; Irizarry RA
    Bioinformatics; 2011 Apr; 27(8):1052-60. PubMed ID: 21478196
    [TBL] [Abstract][Full Text] [Related]  

  • 60. cn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate.
    Clevert DA; Mitterecker A; Mayr A; Klambauer G; Tuefferd M; De Bondt A; Talloen W; Göhlmann H; Hochreiter S
    Nucleic Acids Res; 2011 Jul; 39(12):e79. PubMed ID: 21486749
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.