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 *

163 related articles for article (PubMed ID: 24667782)

  • 21. Assessing the Value of Next-Generation Sequencing Tests in a Dynamic Environment.
    Burris HA; Saltz LB; Yu PP
    Am Soc Clin Oncol Educ Book; 2018 May; 38():139-146. PubMed ID: 30231307
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Impact of the sequencing method on the detection and interpretation of mitochondrial DNA length heteroplasmy.
    Sturk-Andreaggi K; Parson W; Allen M; Marshall C
    Forensic Sci Int Genet; 2020 Jan; 44():102205. PubMed ID: 31783338
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders.
    Cui H; Li F; Chen D; Wang G; Truong CK; Enns GM; Graham B; Milone M; Landsverk ML; Wang J; Zhang W; Wong LJ
    Genet Med; 2013 May; 15(5):388-94. PubMed ID: 23288206
    [TBL] [Abstract][Full Text] [Related]  

  • 24. From Forensics to Clinical Research: Expanding the Variant Calling Pipeline for the Precision ID mtDNA Whole Genome Panel.
    Cortes-Figueiredo F; Carvalho FS; Fonseca AC; Paul F; Ferro JM; Schönherr S; Weissensteiner H; Morais VA
    Int J Mol Sci; 2021 Nov; 22(21):. PubMed ID: 34769461
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels.
    Kerkhof J; Schenkel LC; Reilly J; McRobbie S; Aref-Eshghi E; Stuart A; Rupar CA; Adams P; Hegele RA; Lin H; Rodenhiser D; Knoll J; Ainsworth PJ; Sadikovic B
    J Mol Diagn; 2017 Nov; 19(6):905-920. PubMed ID: 28818680
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
    Hassan SM; Vossen RH; Chessa R; den Dunnen JT; Bakker E; Giordano PC; Harteveld CL
    Blood Cells Mol Dis; 2014 Sep; 53(3):133-7. PubMed ID: 24880717
    [TBL] [Abstract][Full Text] [Related]  

  • 27. mit-o-matic: a comprehensive computational pipeline for clinical evaluation of mitochondrial variations from next-generation sequencing datasets.
    Vellarikkal SK; Dhiman H; Joshi K; Hasija Y; Sivasubbu S; Scaria V
    Hum Mutat; 2015 Apr; 36(4):419-24. PubMed ID: 25677119
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Massive parallel sequencing of human whole mitochondrial genomes with Ion Torrent technology: an optimized workflow for Anthropological and Population Genetics studies.
    De Fanti S; Vianello D; Giuliani C; Quagliariello A; Cherubini A; Sevini F; Iaquilano N; Franceschi C; Sazzini M; Luiselli D
    Mitochondrial DNA A DNA Mapp Seq Anal; 2017 Nov; 28(6):843-850. PubMed ID: 27822964
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory.
    Mehrotra M; Duose DY; Singh RR; Barkoh BA; Manekia J; Harmon MA; Patel KP; Routbort MJ; Medeiros LJ; Wistuba II; Luthra R
    PLoS One; 2017; 12(8):e0181968. PubMed ID: 28767674
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution.
    Santibanez-Koref M; Griffin H; Turnbull DM; Chinnery PF; Herbert M; Hudson G
    Mitochondrion; 2019 May; 46():302-306. PubMed ID: 30098421
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Highly accurate mtGenome haplotypes from long-read SMRT sequencing can distinguish between monozygotic twins.
    Chen L; Wang J; Tan L; Lu C; Fu G; Fu L; Zhang X; Wang Q; Ma C; Cong B; Li S
    Forensic Sci Int Genet; 2020 Jul; 47():102306. PubMed ID: 32438082
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance.
    Minarik G; Repiska G; Hyblova M; Nagyova E; Soltys K; Budis J; Duris F; Sysak R; Gerykova Bujalkova M; Vlkova-Izrael B; Biro O; Nagy B; Szemes T
    PLoS One; 2015; 10(12):e0144811. PubMed ID: 26669558
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Development of a next-generation sequencing method for BRCA mutation screening: a comparison between a high-throughput and a benchtop platform.
    Chan M; Ji SM; Yeo ZX; Gan L; Yap E; Yap YS; Ng R; Tan PH; Ho GH; Ang P; Lee AS
    J Mol Diagn; 2012 Nov; 14(6):602-12. PubMed ID: 22921312
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Full mtDNA genome sequencing of Brazilian admixed populations: A forensic-focused evaluation of a MPS application as an alternative to Sanger sequencing methods.
    Avila E; Graebin P; Chemale G; Freitas J; Kahmann A; Alho CS
    Forensic Sci Int Genet; 2019 Sep; 42():154-164. PubMed ID: 31325893
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Approaches to Whole Mitochondrial Genome Sequencing on the Oxford Nanopore MinION.
    Zascavage RR; Hall CL; Thorson K; Mahmoud M; Sedlazeck FJ; Planz JV
    Curr Protoc Hum Genet; 2019 Dec; 104(1):e94. PubMed ID: 31743587
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Single-Center Experience with a Targeted Next Generation Sequencing Assay for Assessment of Relevant Somatic Alterations in Solid Tumors.
    Paasinen-Sohns A; Koelzer VH; Frank A; Schafroth J; Gisler A; Sachs M; Graber A; Rothschild SI; Wicki A; Cathomas G; Mertz KD
    Neoplasia; 2017 Mar; 19(3):196-206. PubMed ID: 28161563
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
    Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
    Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies.
    Millat G; Chanavat V; Rousson R
    Clin Chim Acta; 2014 Jun; 433():266-71. PubMed ID: 24721642
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Next-generation sequencing identifies novel mitochondrial variants in pituitary adenomas.
    Németh K; Darvasi O; Likó I; Szücs N; Czirják S; Reiniger L; Szabó B; Kurucz PA; Krokker L; Igaz P; Patócs A; Butz H
    J Endocrinol Invest; 2019 Aug; 42(8):931-940. PubMed ID: 30684245
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing.
    Mu W; Lu HM; Chen J; Li S; Elliott AM
    J Mol Diagn; 2016 Nov; 18(6):923-932. PubMed ID: 27720647
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.