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 *

114 related articles for article (PubMed ID: 28361702)

  • 1. A sequence-based method to predict the impact of regulatory variants using random forest.
    Liu Q; Gan M; Jiang R
    BMC Syst Biol; 2017 Mar; 11(Suppl 2):7. PubMed ID: 28361702
    [TBL] [Abstract][Full Text] [Related]  

  • 2. GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding.
    Zeng H; Hashimoto T; Kang DD; Gifford DK
    Bioinformatics; 2016 Feb; 32(4):490-6. PubMed ID: 26476779
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Integrative functional genomics identifies regulatory genetic variant modulating RAB31 expression and altering susceptibility to breast cancer.
    Zhang Y; Yang B; Cheng X; Liu L; Zhu Y; Gong Y; Yang Y; Tian J; Peng X; Zou D; Yang L; Mei S; Wang X; Lou J; Ke J; Li J; Gong J; Chang J; Yuan P; Zhong R
    Mol Carcinog; 2018 Dec; 57(12):1845-1854. PubMed ID: 30182384
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A method to predict the impact of regulatory variants from DNA sequence.
    Lee D; Gorkin DU; Baker M; Strober BJ; Asoni AL; McCallion AS; Beer MA
    Nat Genet; 2015 Aug; 47(8):955-61. PubMed ID: 26075791
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression.
    Cowper-Sal lari R; Zhang X; Wright JB; Bailey SD; Cole MD; Eeckhoute J; Moore JH; Lupien M
    Nat Genet; 2012 Nov; 44(11):1191-8. PubMed ID: 23001124
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Computational identification of deleterious synonymous variants in human genomes using a feature-based approach.
    Shi F; Yao Y; Bin Y; Zheng CH; Xia J
    BMC Med Genomics; 2019 Jan; 12(Suppl 1):12. PubMed ID: 30704475
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A functional link between FOXA1 and breast cancer SNPs.
    Katika MR; Hurtado A
    Breast Cancer Res; 2013 Feb; 15(1):303. PubMed ID: 23427833
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetic and genetic alterations and their influence on gene regulation in chronic lymphocytic leukemia.
    Huang D; Ovcharenko I
    BMC Genomics; 2017 Mar; 18(1):236. PubMed ID: 28302063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks.
    Kelley DR; Snoek J; Rinn JL
    Genome Res; 2016 Jul; 26(7):990-9. PubMed ID: 27197224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Computational analyses of type 2 diabetes-associated loci identified by genome-wide association studies.
    Cheng M; Liu X; Yang M; Han L; Xu A; Huang Q
    J Diabetes; 2017 Apr; 9(4):362-377. PubMed ID: 27121852
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deep sequencing of Danish Holstein dairy cattle for variant detection and insight into potential loss-of-function variants in protein coding genes.
    Das A; Panitz F; Gregersen VR; Bendixen C; Holm LE
    BMC Genomics; 2015 Dec; 16():1043. PubMed ID: 26645365
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Predicting the recurrence of noncoding regulatory mutations in cancer.
    Yang W; Bang H; Jang K; Sung MK; Choi JK
    BMC Bioinformatics; 2016 Dec; 17(1):492. PubMed ID: 27912731
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SNP selection and classification of genome-wide SNP data using stratified sampling random forests.
    Wu Q; Ye Y; Liu Y; Ng MK
    IEEE Trans Nanobioscience; 2012 Sep; 11(3):216-27. PubMed ID: 22987127
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulatory Single-Nucleotide Variant Predictor Increases Predictive Performance of Functional Regulatory Variants.
    Peterson TA; Mort M; Cooper DN; Radivojac P; Kann MG; Mooney SD
    Hum Mutat; 2016 Nov; 37(11):1137-1143. PubMed ID: 27406314
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
    Li MJ; Yan B; Sham PC; Wang J
    Brief Bioinform; 2015 May; 16(3):393-412. PubMed ID: 24916300
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic prediction using preselected DNA variants from a GWAS with whole-genome sequence data in Holstein-Friesian cattle.
    Veerkamp RF; Bouwman AC; Schrooten C; Calus MP
    Genet Sel Evol; 2016 Dec; 48(1):95. PubMed ID: 27905878
    [TBL] [Abstract][Full Text] [Related]  

  • 17. KinMutRF: a random forest classifier of sequence variants in the human protein kinase superfamily.
    Pons T; Vazquez M; Matey-Hernandez ML; Brunak S; Valencia A; Izarzugaza JM
    BMC Genomics; 2016 Jun; 17 Suppl 2(Suppl 2):396. PubMed ID: 27357839
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach.
    McCauley JL; Kenealy SJ; Margulies EH; Schnetz-Boutaud N; Gregory SG; Hauser SL; Oksenberg JR; Pericak-Vance MA; Haines JL; Mortlock DP
    BMC Genomics; 2007 Aug; 8():266. PubMed ID: 17683615
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maximal conditional chi-square importance in random forests.
    Wang M; Chen X; Zhang H
    Bioinformatics; 2010 Mar; 26(6):831-7. PubMed ID: 20130032
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Endometrial vezatin and its association with endometriosis risk.
    Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
    Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.