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 *

70 related articles for article (PubMed ID: 25519414)

  • 1. A multi-level model for analyzing whole genome sequencing family data with longitudinal traits.
    Chen T; Santawisook P; Wu Z
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S86. PubMed ID: 25519414
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Longitudinal data analysis for genetic studies in the whole-genome sequencing era.
    Wu Z; Hu Y; Melton PE
    Genet Epidemiol; 2014 Sep; 38 Suppl 1():S74-80. PubMed ID: 25112193
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Extended T(2) tests for longitudinal family data in whole genome sequencing studies.
    Liu Y; Xuan J; Wu Z
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S40. PubMed ID: 25519385
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole-genome characterization in pedigreed non-human primates using genotyping-by-sequencing (GBS) and imputation.
    Bimber BN; Raboin MJ; Letaw J; Nevonen KA; Spindel JE; McCouch SR; Cervera-Juanes R; Spindel E; Carbone L; Ferguson B; Vinson A
    BMC Genomics; 2016 Aug; 17(1):676. PubMed ID: 27558348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Discovering human germ cell mutagens with whole genome sequencing: Insights from power calculations reveal the importance of controlling for between-family variability.
    Webster RJ; Williams A; Marchetti F; Yauk CL
    Mutat Res Genet Toxicol Environ Mutagen; 2018 Jul; 831():24-32. PubMed ID: 29875074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparison of multilevel modeling and the family-based association test for identifying genetic variants associated with systolic and diastolic blood pressure using Genetic Analysis Workshop 18 simulated data.
    Wang J; Yu R; Shete S
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S30. PubMed ID: 25519380
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method.
    Yan Q; Weeks DE; Celedón JC; Tiwari HK; Li B; Wang X; Lin WY; Lou XY; Gao G; Chen W; Liu N
    Genetics; 2015 Dec; 201(4):1329-39. PubMed ID: 26482791
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.
    Sul JH; Cade BE; Cho MH; Qiao D; Silverman EK; Redline S; Sunyaev S
    Am J Hum Genet; 2016 Oct; 99(4):846-859. PubMed ID: 27666371
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals.
    Darst BF; Engelman CD
    BMC Proc; 2016; 10(Suppl 7):203-207. PubMed ID: 27980637
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incorporating ENCODE information into association analysis of whole genome sequencing data.
    Kim T; Wei P
    BMC Proc; 2016; 10(Suppl 7):257-261. PubMed ID: 27980646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare variant association test with multiple phenotypes.
    Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
    Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CollapsABEL: an R library for detecting compound heterozygote alleles in genome-wide association studies.
    Zhong K; Karssen LC; Kayser M; Liu F
    BMC Bioinformatics; 2016 Apr; 17():156. PubMed ID: 27059780
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole genome sequencing and rare variant analysis in essential tremor families.
    Odgerel Z; Sonti S; Hernandez N; Park J; Ottman R; Louis ED; Clark LN
    PLoS One; 2019; 14(8):e0220512. PubMed ID: 31404076
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-genome sequence-based genomic prediction in laying chickens with different genomic relationship matrices to account for genetic architecture.
    Ni G; Cavero D; Fangmann A; Erbe M; Simianer H
    Genet Sel Evol; 2017 Jan; 49(1):8. PubMed ID: 28093063
    [TBL] [Abstract][Full Text] [Related]  

  • 15. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
    Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid BM; Bjerin O; Gustavsson P; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
    Genome Med; 2019 Nov; 11(1):68. PubMed ID: 31694722
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Comparison of Statistical Methods for the Discovery of Genetic Risk Factors Using Longitudinal Family Study Designs.
    Burkett KM; Roy-Gagnon MH; Lefebvre JF; Wang C; Fontaine-Bisson B; Dubois L
    Front Immunol; 2015; 6():589. PubMed ID: 26635803
    [TBL] [Abstract][Full Text] [Related]  

  • 17. On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.
    Loehlein Fier H; Prokopenko D; Hecker J; Cho MH; Silverman EK; Weiss ST; Tanzi RE; Lange C
    Genet Epidemiol; 2017 May; 41(4):332-340. PubMed ID: 28318110
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease.
    Ellingford JM; Barton S; Bhaskar S; Williams SG; Sergouniotis PI; O'Sullivan J; Lamb JA; Perveen R; Hall G; Newman WG; Bishop PN; Roberts SA; Leach R; Tearle R; Bayliss S; Ramsden SC; Nemeth AH; Black GC
    Ophthalmology; 2016 May; 123(5):1143-50. PubMed ID: 26872967
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meta-analysis of Complex Diseases at Gene Level with Generalized Functional Linear Models.
    Fan R; Wang Y; Chiu CY; Chen W; Ren H; Li Y; Boehnke M; Amos CI; Moore JH; Xiong M
    Genetics; 2016 Feb; 202(2):457-70. PubMed ID: 26715663
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A goodness-of-fit association test for whole genome sequencing data.
    Yang L; Xuan J; Wu Z
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S51. PubMed ID: 25519389
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.