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 *

157 related articles for article (PubMed ID: 24067417)

  • 1. Construction and analysis of single nucleotide polymorphism-single nucleotide polymorphism interaction networks.
    Liu Y; Li X; Liu Z; Chen L; Ng MK
    IET Syst Biol; 2013 Oct; 7(5):170-81. PubMed ID: 24067417
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shrunken methodology to genome-wide SNPs selection and construction of SNPs networks.
    Liu Y; Ng M
    BMC Syst Biol; 2010 Sep; 4 Suppl 2(Suppl 2):S5. PubMed ID: 20840732
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Learning gene networks under SNP perturbations using eQTL datasets.
    Zhang L; Kim S
    PLoS Comput Biol; 2014 Feb; 10(2):e1003420. PubMed ID: 24586125
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combination of microRNA expression profiling with genome-wide SNP genotyping to construct a coronary artery disease-related miRNA-miRNA synergistic network.
    Hua L; Xia H; Zhou P; Li D; Li L
    Biosci Trends; 2014 Dec; 8(6):297-307. PubMed ID: 25641175
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data.
    Zhao X; Luan YZ; Zuo X; Chen YD; Qin J; Jin L; Tan Y; Lin M; Zhang N; Liang Y; Rao SQ
    Genomics Proteomics Bioinformatics; 2016 Dec; 14(6):349-356. PubMed ID: 27965104
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Weighted Interaction SNP Hub (WISH) network method for building genetic networks for complex diseases and traits using whole genome genotype data.
    Kogelman LJ; Kadarmideen HN
    BMC Syst Biol; 2014; 8 Suppl 2(Suppl 2):S5. PubMed ID: 25032480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of susceptibility modules for coronary artery disease using a genome wide integrated network analysis.
    Duan S; Luo X; Dong C
    Gene; 2013 Dec; 531(2):347-54. PubMed ID: 23994195
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y; Segal MR; Yang YH; Yeh RF
    Bioinformatics; 2007 Jun; 23(12):1459-67. PubMed ID: 17459966
    [TBL] [Abstract][Full Text] [Related]  

  • 9. WISH-R- a fast and efficient tool for construction of epistatic networks for complex traits and diseases.
    Carmelo VAO; Kogelman LJA; Madsen MB; Kadarmideen HN
    BMC Bioinformatics; 2018 Jul; 19(1):277. PubMed ID: 30064383
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A genotype calling algorithm for affymetrix SNP arrays.
    Rabbee N; Speed TP
    Bioinformatics; 2006 Jan; 22(1):7-12. PubMed ID: 16267090
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Discovering Genetic Factors for psoriasis through exhaustively searching for significant second order SNP-SNP interactions.
    Lee KY; Leung KS; Tang NLS; Wong MH
    Sci Rep; 2018 Oct; 8(1):15186. PubMed ID: 30315195
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data.
    Liu Y; Maxwell S; Feng T; Zhu X; Elston RC; Koyutürk M; Chance MR
    BMC Syst Biol; 2012; 6 Suppl 3(Suppl 3):S15. PubMed ID: 23281810
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotype prediction by integrative network analysis of SNP and gene expression microarrays.
    Chang HH; McGeachie M
    Annu Int Conf IEEE Eng Med Biol Soc; 2011; 2011():6849-52. PubMed ID: 22255912
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrative gene ontology and network analysis of coronary artery disease associated genes suggests potential role of ErbB pathway gene EGFR.
    Ghatge M; Nair J; Sharma A; Vangala RK
    Mol Med Rep; 2018 Mar; 17(3):4253-4264. PubMed ID: 29328373
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SNP and gene networks construction and analysis from classification of copy number variations data.
    Liu Y; Lee YF; Ng MK
    BMC Bioinformatics; 2011; 12 Suppl 5(Suppl 5):S4. PubMed ID: 21989070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis.
    Suzuki S; Yoshimura M; Nakayama M; Abe K; Yamamuro M; Nagayoshi Y; Kojima S; Kaikita K; Sugiyama S; Yasue H; Ogawa H
    Pharmacogenet Genomics; 2007 Nov; 17(11):919-30. PubMed ID: 18075462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Integrative construction of regulatory region networks in 127 human reference epigenomes by matrix factorization.
    Liu D; Davila-Velderrain J; Zhang Z; Kellis M
    Nucleic Acids Res; 2019 Aug; 47(14):7235-7246. PubMed ID: 31265076
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of breast cancer susceptibility using improved genetic algorithms to generate genotype SNP barcodes.
    Yang CH; Lin YD; Chuang LY; Chang HW
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(2):361-71. PubMed ID: 23929860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inferring polymorphism-induced regulatory gene networks active in human lymphocyte cell lines by weighted linear mixed model analysis of multiple RNA-Seq datasets.
    Zhang W; Edwards A; Flemington EK; Zhang K
    PLoS One; 2013; 8(10):e78868. PubMed ID: 24205334
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide association data classification and SNPs selection using two-stage quality-based Random Forests.
    Nguyen TT; Huang J; Wu Q; Nguyen T; Li M
    BMC Genomics; 2015; 16 Suppl 2(Suppl 2):S5. PubMed ID: 25708662
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.