BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 28991724)

  • 1. 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]  

  • 2. 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]  

  • 3. Copy number variations and human genetic disease.
    Mikhail FM
    Curr Opin Pediatr; 2014 Dec; 26(6):646-52. PubMed ID: 25198053
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health.
    Saitou M; Gokcumen O
    J Mol Evol; 2020 Jan; 88(1):104-119. PubMed ID: 31522275
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.
    Nygaard M; Debrabant B; Tan Q; Deelen J; Andersen-Ranberg K; de Craen AJ; Beekman M; Jeune B; Slagboom PE; Christensen K; Christiansen L
    Aging Cell; 2016 Feb; 15(1):49-55. PubMed ID: 26446717
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CNVinspector: a web-based tool for the interactive evaluation of copy number variations in single patients and in cohorts.
    Knierim E; Schwarz JM; Schuelke M; Seelow D
    J Med Genet; 2013 Aug; 50(8):529-33. PubMed ID: 23729504
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
    Hosak L; Silhan P; Hosakova J
    Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The impact of human copy number variation on a new era of genetic testing.
    Choy KW; Setlur SR; Lee C; Lau TK
    BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Genomic population structure and prevalence of copy number variations in South African Nguni cattle.
    Wang MD; Dzama K; Hefer CA; Muchadeyi FC
    BMC Genomics; 2015 Nov; 16():894. PubMed ID: 26531252
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Parametric modeling of whole-genome sequencing data for CNV identification.
    Vardhanabhuti S; Jeng XJ; Wu Y; Li H
    Biostatistics; 2014 Jul; 15(3):427-41. PubMed ID: 24478395
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variation contributes to cryptic genetic variation in outbreak lineages of Cryptococcus gattii from the North American Pacific Northwest.
    Steenwyk JL; Soghigian JS; Perfect JR; Gibbons JG
    BMC Genomics; 2016 Sep; 17(1):700. PubMed ID: 27590805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. DNA sequence features underlying large-scale duplications and deletions in human.
    Kołomański M; Szyda J; Frąszczak M; Mielczarek M
    J Appl Genet; 2022 Sep; 63(3):527-533. PubMed ID: 35590085
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Current analysis platforms and methods for detecting copy number variation.
    Li W; Olivier M
    Physiol Genomics; 2013 Jan; 45(1):1-16. PubMed ID: 23132758
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CNVs into the wild: screening the genomes of conifer trees (Picea spp.) reveals fewer gene copy number variations in hybrids and links to adaptation.
    Prunier J; Caron S; MacKay J
    BMC Genomics; 2017 Jan; 18(1):97. PubMed ID: 28100184
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Characterization of copy number-stable regions in the human genome.
    Johansson AC; Feuk L
    Hum Mutat; 2011 Aug; 32(8):947-55. PubMed ID: 21542059
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.