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 *

342 related articles for article (PubMed ID: 31996208)

  • 1. Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients.
    Yao RA; Akinrinade O; Chaix M; Mital S
    BMC Med Genomics; 2020 Jan; 13(1):11. PubMed ID: 31996208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Validated WGS and WES protocols proved saliva-derived gDNA as an equivalent to blood-derived gDNA for clinical and population genomic analyses.
    Kvapilova K; Misenko P; Radvanszky J; Brzon O; Budis J; Gazdarica J; Pos O; Korabecna M; Kasny M; Szemes T; Kvapil P; Paces J; Kozmik Z
    BMC Genomics; 2024 Feb; 25(1):187. PubMed ID: 38365587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impact of DNA source on genetic variant detection from human whole-genome sequencing data.
    Trost B; Walker S; Haider SA; Sung WWL; Pereira S; Phillips CL; Higginbotham EJ; Strug LJ; Nguyen C; Raajkumar A; Szego MJ; Marshall CR; Scherer SW
    J Med Genet; 2019 Dec; 56(12):809-817. PubMed ID: 31515274
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
    Hollegaard MV; Grauholm J; Nielsen R; Grove J; Mandrup S; Hougaard DM
    Mol Genet Metab; 2013; 110(1-2):65-72. PubMed ID: 23830478
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Empirical evaluation of variant calling accuracy using ultra-deep whole-genome sequencing data.
    Kishikawa T; Momozawa Y; Ozeki T; Mushiroda T; Inohara H; Kamatani Y; Kubo M; Okada Y
    Sci Rep; 2019 Feb; 9(1):1784. PubMed ID: 30741997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contaminating DNA in human saliva alters the detection of variants from whole genome sequencing.
    Samson CA; Whitford W; Snell RG; Jacobsen JC; Lehnert K
    Sci Rep; 2020 Nov; 10(1):19255. PubMed ID: 33159102
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variant detection sensitivity and biases in whole genome and exome sequencing.
    Meynert AM; Ansari M; FitzPatrick DR; Taylor MS
    BMC Bioinformatics; 2014 Jul; 15(1):247. PubMed ID: 25038816
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.
    Byrska-Bishop M; Evani US; Zhao X; Basile AO; Abel HJ; Regier AA; Corvelo A; Clarke WE; Musunuri R; Nagulapalli K; Fairley S; Runnels A; Winterkorn L; Lowy E; ; Paul Flicek ; Germer S; Brand H; Hall IM; Talkowski ME; Narzisi G; Zody MC
    Cell; 2022 Sep; 185(18):3426-3440.e19. PubMed ID: 36055201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A clinically validated whole genome pipeline for structural variant detection and analysis.
    Neerman N; Faust G; Meeks N; Modai S; Kalfon L; Falik-Zaccai T; Kaplun A
    BMC Genomics; 2019 Jul; 20(Suppl 8):545. PubMed ID: 31307387
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of saliva as a source of accurate whole-genome and microbiome sequencing data.
    Herzig AF; Velo-Suárez L; Le Folgoc G; Boland A; Blanché H; Olaso R; Le Roux L; Delmas C; Goldberg M; Zins M; Lethimonnier F; Deleuze JF; Génin E
    Genet Epidemiol; 2021 Jul; 45(5):537-548. PubMed ID: 33998042
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-genome sequencing based on formalin-fixed paraffin-embedded endomyocardial biopsies for genetic studies on outcomes after heart transplantation.
    Zar G; Smith JG; Smith ML; Andersson B; Nilsson J
    PLoS One; 2019; 14(6):e0217747. PubMed ID: 31166960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 5WBF: a low-cost and straightforward whole blood filtration method suitable for whole-genome sequencing of Plasmodium falciparum clinical isolates.
    Coppée R; Mama A; Sarrasin V; Kamaliddin C; Adoux L; Palazzo L; Ndam NT; Letourneur F; Ariey F; Houzé S; Clain J
    Malar J; 2022 Feb; 21(1):51. PubMed ID: 35172825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Computational pharmacogenotype extraction from clinical next-generation sequencing.
    Shugg T; Ly RC; Osei W; Rowe EJ; Granfield CA; Lynnes TC; Medeiros EB; Hodge JC; Breman AM; Schneider BP; Sahinalp SC; Numanagić I; Salisbury BA; Bray SM; Ratcliff R; Skaar TC
    Front Oncol; 2023; 13():1199741. PubMed ID: 37469403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Empirical design of a variant quality control pipeline for whole genome sequencing data using replicate discordance.
    Adelson RP; Renton AE; Li W; Barzilai N; Atzmon G; Goate AM; Davies P; Freudenberg-Hua Y
    Sci Rep; 2019 Nov; 9(1):16156. PubMed ID: 31695094
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Medical implications of technical accuracy in genome sequencing.
    Goldfeder RL; Priest JR; Zook JM; Grove ME; Waggott D; Wheeler MT; Salit M; Ashley EA
    Genome Med; 2016 Mar; 8(1):24. PubMed ID: 26932475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
    Naj AC; Lin H; Vardarajan BN; White S; Lancour D; Ma Y; Schmidt M; Sun F; Butkiewicz M; Bush WS; Kunkle BW; Malamon J; Amin N; Choi SH; Hamilton-Nelson KL; van der Lee SJ; Gupta N; Koboldt DC; Saad M; Wang B; Nato AQ; Sohi HK; Kuzma A; ; Wang LS; Cupples LA; van Duijn C; Seshadri S; Schellenberg GD; Boerwinkle E; Bis JC; Dupuis J; Salerno WJ; Wijsman EM; Martin ER; DeStefano AL
    Genomics; 2019 Jul; 111(4):808-818. PubMed ID: 29857119
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-genome sequencing of phenotypically distinct inflammatory breast cancers reveals similar genomic alterations to non-inflammatory breast cancers.
    Li X; Kumar S; Harmanci A; Li S; Kitchen RR; Zhang Y; Wali VB; Reddy SM; Woodward WA; Reuben JM; Rozowsky J; Hatzis C; Ueno NT; Krishnamurthy S; Pusztai L; Gerstein M
    Genome Med; 2021 Apr; 13(1):70. PubMed ID: 33902690
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.