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 *

58 related articles for article (PubMed ID: 25546614)

  • 1. CPAS: a trans-omics pathway analysis tool for jointly analyzing DNA copy number variations and mRNA expression profiles data.
    Zhang F; Xiao X; Hao J; Wang S; Wen Y; Guo X
    J Biomed Inform; 2015 Feb; 53():363-6. PubMed ID: 25546614
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. COKGEN: a software for the identification of rare copy number variation from SNP microarrays.
    Yavaş G; Koyutürk M; Ozsoyoğlu M; Gould MP; Laframboise T
    Pac Symp Biocomput; 2010; ():371-82. PubMed ID: 19908389
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trans-omics pathway analysis suggests that eQTLs contribute to chondrocyte apoptosis of Kashin-Beck disease through regulating apoptosis pathway expression.
    Zhang F; Wen Y; Guo X; Yang T; Shen H; Chen X; Tan L; Tian Q; Deng HW
    Gene; 2014 Dec; 553(2):166-9. PubMed ID: 25307768
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Regulatory gene networks and signaling pathways from primary osteoarthritis and Kashin-Beck disease, an endemic osteoarthritis, identified by three analysis software.
    Wang S; Duan C; Zhang F; Ma W; Guo X
    Gene; 2013 Jan; 512(1):89-96. PubMed ID: 23069848
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A method for generating new datasets based on copy number for cancer analysis.
    Kim S; Kon M; Kang H
    Biomed Res Int; 2015; 2015():467514. PubMed ID: 25949998
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide copy number analysis in a family with p.G533C RET mutation and medullary thyroid carcinoma identified regions potentially associated with a higher predisposition to lymph node metastasis.
    Araujo AN; Moraes L; França MI; Hakonarson H; Li J; Pellegrino R; Maciel RM; Cerutti JM
    J Clin Endocrinol Metab; 2014 Jun; 99(6):E1104-12. PubMed ID: 24601688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.
    Wu Y; Fan H; Jing S; Xia J; Chen Y; Zhang L; Gao X; Li J; Gao H; Ren H
    Anim Genet; 2015 Jun; 46(3):289-98. PubMed ID: 25917301
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression profiles of genes involved in apoptosis and selenium metabolism in articular cartilage of patients with Kashin-Beck osteoarthritis.
    Wu SX; Wang WZ; Zhang F; Wu CY; Dennis BS; Qu CJ; Bai YD; Guo X
    Gene; 2014 Feb; 535(2):124-30. PubMed ID: 24316489
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. ShinyCNV: a Shiny/R application to view and annotate DNA copy number variations.
    Gu Z; Mullighan CG
    Bioinformatics; 2019 Jan; 35(1):126-129. PubMed ID: 30561549
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. MILANO--custom annotation of microarray results using automatic literature searches.
    Rubinstein R; Simon I
    BMC Bioinformatics; 2005 Jan; 6():12. PubMed ID: 15661078
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrated analysis of SNP, CNV and gene expression data in genetic association studies.
    Momtaz R; Ghanem NM; El-Makky NM; Ismail MA
    Clin Genet; 2018 Mar; 93(3):557-566. PubMed ID: 28685831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Integrative clustering of multi-level 'omic data based on non-negative matrix factorization algorithm.
    Chalise P; Fridley BL
    PLoS One; 2017; 12(5):e0176278. PubMed ID: 28459819
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of copy number variation-driven genes for liver cancer via bioinformatics analysis.
    Lu X; Ye K; Zou K; Chen J
    Oncol Rep; 2014 Nov; 32(5):1845-52. PubMed ID: 25174835
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The variation game: Cracking complex genetic disorders with NGS and omics data.
    Cui H; Dhroso A; Johnson N; Korkin D
    Methods; 2015 Jun; 79-80():18-31. PubMed ID: 25944472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Associations of MYH3 gene copy number variations with transcriptional expression and growth traits in Chinese cattle.
    Xu Y; Shi T; Cai H; Zhou Y; Lan X; Zhang C; Lei C; Qi X; Chen H
    Gene; 2014 Feb; 535(2):106-11. PubMed ID: 24316128
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene expression analysis in clear cell renal cell carcinoma using gene set enrichment analysis for biostatistical management.
    Maruschke M; Reuter D; Koczan D; Hakenberg OW; Thiesen HJ
    BJU Int; 2011 Jul; 108(2 Pt 2):E29-35. PubMed ID: 21435154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 3.