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 *

187 related articles for article (PubMed ID: 28532386)

  • 21. An evaluation of sequencing coverage and genotyping strategies to assess neutral and adaptive diversity.
    Benjelloun B; Boyer F; Streeter I; Zamani W; Engelen S; Alberti A; Alberto FJ; BenBati M; Ibnelbachyr M; Chentouf M; Bechchari A; Rezaei HR; Naderi S; Stella A; Chikhi A; Clarke L; Kijas J; Flicek P; Taberlet P; Pompanon F
    Mol Ecol Resour; 2019 Nov; 19(6):1497-1515. PubMed ID: 31359622
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-genome sequencing in French Canadians from Quebec.
    Low-Kam C; Rhainds D; Lo KS; Provost S; Mongrain I; Dubois A; Perreault S; Robinson JF; Hegele RA; Dubé MP; Tardif JC; Lettre G
    Hum Genet; 2016 Nov; 135(11):1213-1221. PubMed ID: 27376640
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.
    Emde AK; Phipps-Green A; Cadzow M; Gallagher CS; Major TJ; Merriman ME; Topless RK; Takei R; Dalbeth N; Murphy R; Stamp LK; de Zoysa J; Wilcox PL; Fox K; Wasik KA; Merriman TR; Castel SE
    BMC Genomics; 2021 Nov; 22(1):666. PubMed ID: 34719381
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A hybrid computational strategy to address WGS variant analysis in >5000 samples.
    Huang Z; Rustagi N; Veeraraghavan N; Carroll A; Gibbs R; Boerwinkle E; Venkata MG; Yu F
    BMC Bioinformatics; 2016 Sep; 17(1):361. PubMed ID: 27612449
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A study on fast calling variants from next-generation sequencing data using decision tree.
    Li Z; Wang Y; Wang F
    BMC Bioinformatics; 2018 Apr; 19(1):145. PubMed ID: 29673316
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.
    Hanks SC; Forer L; Schönherr S; LeFaive J; Martins T; Welch R; Gagliano Taliun SA; Braff D; Johnsen JM; Kenny EE; Konkle BA; Laakso M; Loos RFJ; McCarroll S; Pato C; Pato MT; Smith AV; ; Boehnke M; Scott LJ; Fuchsberger C
    Am J Hum Genet; 2022 Sep; 109(9):1653-1666. PubMed ID: 35981533
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel.
    Huang J; Howie B; McCarthy S; Memari Y; Walter K; Min JL; Danecek P; Malerba G; Trabetti E; Zheng HF; ; Gambaro G; Richards JB; Durbin R; Timpson NJ; Marchini J; Soranzo N
    Nat Commun; 2015 Sep; 6():8111. PubMed ID: 26368830
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project.
    Yasuda J; Katsuoka F; Danjoh I; Kawai Y; Kojima K; Nagasaki M; Saito S; Yamaguchi-Kabata Y; Tadaka S; Motoike IN; Kumada K; Sakurai-Yageta M; Tanabe O; Fuse N; Tamiya G; Higasa K; Matsuda F; Yasuda N; Iwasaki M; Sasaki M; Shimizu A; Kinoshita K; Yamamoto M
    BMC Genomics; 2018 Jul; 19(1):551. PubMed ID: 30041597
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.
    Cirino AL; Lakdawala NK; McDonough B; Conner L; Adler D; Weinfeld M; O'Gara P; Rehm HL; Machini K; Lebo M; Blout C; Green RC; MacRae CA; Seidman CE; Ho CY;
    Circ Cardiovasc Genet; 2017 Oct; 10(5):. PubMed ID: 29030401
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Best practices for analyzing imputed genotypes from low-pass sequencing in dogs.
    Buckley RM; Harris AC; Wang GD; Whitaker DT; Zhang YP; Ostrander EA
    Mamm Genome; 2022 Mar; 33(1):213-229. PubMed ID: 34498136
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection.
    Stubbs A; McClellan EA; Horsman S; Hiltemann SD; Palli I; Nouwens S; Koning AH; Hoogland F; Reumers J; Heijsman D; Swagemakers S; Kremer A; Meijerink J; Lambrechts D; van der Spek PJ
    J Clin Bioinforma; 2012 Nov; 2(1):19. PubMed ID: 23164068
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings.
    Hwang KB; Lee IH; Li H; Won DG; Hernandez-Ferrer C; Negron JA; Kong SW
    Sci Rep; 2019 Mar; 9(1):3219. PubMed ID: 30824715
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project.
    Tantoso E; Wong LP; Li B; Saw WY; Xu W; Little P; Ong RT; Teo YY
    PLoS One; 2014; 9(9):e106681. PubMed ID: 25203698
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals.
    Nagasaki M; Yasuda J; Katsuoka F; Nariai N; Kojima K; Kawai Y; Yamaguchi-Kabata Y; Yokozawa J; Danjoh I; Saito S; Sato Y; Mimori T; Tsuda K; Saito R; Pan X; Nishikawa S; Ito S; Kuroki Y; Tanabe O; Fuse N; Kuriyama S; Kiyomoto H; Hozawa A; Minegishi N; Douglas Engel J; Kinoshita K; Kure S; Yaegashi N; ; Yamamoto M
    Nat Commun; 2015 Aug; 6():8018. PubMed ID: 26292667
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Accuracy of whole-genome sequence imputation using hybrid peeling in large pedigreed livestock populations.
    Ros-Freixedes R; Whalen A; Chen CY; Gorjanc G; Herring WO; Mileham AJ; Hickey JM
    Genet Sel Evol; 2020 Apr; 52(1):17. PubMed ID: 32248811
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequencing and analysis of a South Asian-Indian personal genome.
    Gupta R; Ratan A; Rajesh C; Chen R; Kim HL; Burhans R; Miller W; Santhosh S; Davuluri RV; Butte AJ; Schuster SC; Seshagiri S; Thomas G
    BMC Genomics; 2012 Aug; 13():440. PubMed ID: 22938532
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis.
    Zhou B; Ho SS; Zhang X; Pattni R; Haraksingh RR; Urban AE
    J Med Genet; 2018 Nov; 55(11):735-743. PubMed ID: 30061371
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Very low-depth whole-genome sequencing in complex trait association studies.
    Gilly A; Southam L; Suveges D; Kuchenbaecker K; Moore R; Melloni GEM; Hatzikotoulas K; Farmaki AE; Ritchie G; Schwartzentruber J; Danecek P; Kilian B; Pollard MO; Ge X; Tsafantakis E; Dedoussis G; Zeggini E
    Bioinformatics; 2019 Aug; 35(15):2555-2561. PubMed ID: 30576415
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sequencing whole genomes of the West Javanese population in Indonesia reveals novel variants and improves imputation accuracy.
    Ardiansyah E; Riza AL; Dian S; Ganiem AR; Alisjahbana B; Setiabudiawan TP; van Laarhoven A; van Crevel R; Kumar V
    bioRxiv; 2024 Jun; ():. PubMed ID: 38915501
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.