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 *

278 related articles for article (PubMed ID: 25587064)

  • 1. SeqHBase: a big data toolset for family based sequencing data analysis.
    He M; Person TN; Hebbring SJ; Heinzen E; Ye Z; Schrodi SJ; McPherson EW; Lin SM; Peissig PL; Brilliant MH; O'Rawe J; Robison RJ; Lyon GJ; Wang K
    J Med Genet; 2015 Apr; 52(4):282-8. PubMed ID: 25587064
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene-variant discovery, annotation, prediction, and genotyping.
    Ahmed Z; Renart EG; Mishra D; Zeeshan S
    FEBS Open Bio; 2021 Sep; 11(9):2441-2452. PubMed ID: 34370400
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.
    Lelieveld SH; Spielmann M; Mundlos S; Veltman JA; Gilissen C
    Hum Mutat; 2015 Aug; 36(8):815-22. PubMed ID: 25973577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data.
    Khateb S; Hanany M; Khalaileh A; Beryozkin A; Meyer S; Abu-Diab A; Abu Turky F; Mizrahi-Meissonnier L; Lieberman S; Ben-Yosef T; Banin E; Sharon D
    J Med Genet; 2016 Sep; 53(9):600-7. PubMed ID: 27208209
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Next-generation diagnostics: gene panel, exome, or whole genome?
    Sun Y; Ruivenkamp CA; Hoffer MJ; Vrijenhoek T; Kriek M; van Asperen CJ; den Dunnen JT; Santen GW
    Hum Mutat; 2015 Jun; 36(6):648-55. PubMed ID: 25772376
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data.
    Cherukuri PF; Maduro V; Fuentes-Fajardo KV; Lam K; ; Adams DR; Tifft CJ; Mullikin JC; Gahl WA; Boerkoel CF
    BMC Genomics; 2015 Nov; 16():998. PubMed ID: 26602380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.
    Chou J; Ohsumi TK; Geha RS
    Curr Opin Allergy Clin Immunol; 2012 Dec; 12(6):623-8. PubMed ID: 23095910
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Optimized distributed systems achieve significant performance improvement on sorted merging of massive VCF files.
    Sun X; Gao J; Jin P; Eng C; Burchard EG; Beaty TH; Ruczinski I; Mathias RA; Barnes K; Wang F; Qin ZS;
    Gigascience; 2018 Jun; 7(6):. PubMed ID: 29762754
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Optimizing performance of GATK workflows using Apache Arrow In-Memory data framework.
    Ahmad T; Ahmed N; Al-Ars Z; Hofstee HP
    BMC Genomics; 2020 Nov; 21(Suppl 10):683. PubMed ID: 33208101
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data.
    Ferrarini A; Xumerle L; Griggio F; Garonzi M; Cantaloni C; Centomo C; Vargas SM; Descombes P; Marquis J; Collino S; Franceschi C; Garagnani P; Salisbury BA; Harvey JM; Delledonne M
    PLoS One; 2015; 10(7):e0132180. PubMed ID: 26147798
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. GT-WGS: an efficient and economic tool for large-scale WGS analyses based on the AWS cloud service.
    Wang Y; Li G; Ma M; He F; Song Z; Zhang W; Wu C
    BMC Genomics; 2018 Jan; 19(Suppl 1):959. PubMed ID: 29363427
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Opportunities and challenges of whole-genome and -exome sequencing.
    Petersen BS; Fredrich B; Hoeppner MP; Ellinghaus D; Franke A
    BMC Genet; 2017 Feb; 18(1):14. PubMed ID: 28193154
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical sequencing: is WGS the better WES?
    Meienberg J; Bruggmann R; Oexle K; Matyas G
    Hum Genet; 2016 Mar; 135(3):359-62. PubMed ID: 26742503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing.
    Alfares A; Aloraini T; Subaie LA; Alissa A; Qudsi AA; Alahmad A; Mutairi FA; Alswaid A; Alothaim A; Eyaid W; Albalwi M; Alturki S; Alfadhel M
    Genet Med; 2018 Nov; 20(11):1328-1333. PubMed ID: 29565419
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reducing INDEL calling errors in whole genome and exome sequencing data.
    Fang H; Wu Y; Narzisi G; O'Rawe JA; Barrón LT; Rosenbaum J; Ronemus M; Iossifov I; Schatz MC; Lyon GJ
    Genome Med; 2014; 6(10):89. PubMed ID: 25426171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.