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 *

92 related articles for article (PubMed ID: 31445212)

  • 1. Short DNA Probes Developed for Sample Tracking and Quality Assurance in Gene Panel Testing.
    Fujiki R; Ikeda M; Ohara O
    J Mol Diagn; 2019 Nov; 21(6):1079-1094. PubMed ID: 31445212
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis.
    Schenkel LC; Kerkhof J; Stuart A; Reilly J; Eng B; Woodside C; Levstik A; Howlett CJ; Rupar AC; Knoll JHM; Ainsworth P; Waye JS; Sadikovic B
    J Mol Diagn; 2016 Sep; 18(5):657-667. PubMed ID: 27376475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Role of Quality Control in Targeted Next-generation Sequencing Library Preparation.
    Nietsch R; Haas J; Lai A; Oehler D; Mester S; Frese KS; Sedaghat-Hamedani F; Kayvanpour E; Keller A; Meder B
    Genomics Proteomics Bioinformatics; 2016 Aug; 14(4):200-6. PubMed ID: 27475404
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary Colorectal Cancer Diagnosis by Next-Generation Sequencing.
    Wen T; Ehivet F; Stanislaw C; Mao R; Hegde M
    Curr Protoc; 2023 Dec; 3(12):e941. PubMed ID: 38112503
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. The reliable assurance of detecting somatic mutations in cancer-related genes by next-generation sequencing: the results of external quality assessment in China.
    Zhang R; Ding J; Han Y; Yi L; Xie J; Yang X; Fan G; Wang G; Hao M; Zhang D; Zhang K; Lin G; Li J
    Oncotarget; 2016 Sep; 7(36):58500-58515. PubMed ID: 27542269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (2) - Sample collection, processing and detection].
    Zeng X; Xu Z; Huang H; Qu W; Wu J; Wang J; Gao Y; An D; Wang X; Xiong H; Shen Y; Qi M; Deng X; Xu X; Sun L; Peng Z; Gu W; Huang S; Yu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):339-344. PubMed ID: 32128755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Target capture enrichment of nuclear SNP markers for massively parallel sequencing of degraded and mixed samples.
    Bose N; Carlberg K; Sensabaugh G; Erlich H; Calloway C
    Forensic Sci Int Genet; 2018 May; 34():186-196. PubMed ID: 29524767
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ClinQC: a tool for quality control and cleaning of Sanger and NGS data in clinical research.
    Pandey RV; Pabinger S; Kriegner A; Weinhäusel A
    BMC Bioinformatics; 2016 Feb; 17():56. PubMed ID: 26830926
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid and highly-specific generation of targeted DNA sequencing libraries enabled by linking capture probes with universal primers.
    Pel J; Leung A; Choi WWY; Despotovic M; Ung WL; Shibahara G; Gelinas L; Marziali A
    PLoS One; 2018; 13(12):e0208283. PubMed ID: 30517195
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: Implications for the use of a positive control in a next-generation sequencing procedure.
    Marshall C; Sturk-Andreaggi K; Daniels-Higginbotham J; Oliver RS; Barritt-Ross S; McMahon TP
    Forensic Sci Int Genet; 2017 Nov; 31():198-206. PubMed ID: 29101892
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Targeted High-Throughput Next-Generation Sequencing Panel for Clinical Screening of Mutations, Gene Amplifications, and Fusions in Solid Tumors.
    Luthra R; Patel KP; Routbort MJ; Broaddus RR; Yau J; Simien C; Chen W; Hatfield DZ; Medeiros LJ; Singh RR
    J Mol Diagn; 2017 Mar; 19(2):255-264. PubMed ID: 28017569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Performance evaluation of commercial library construction kits for PCR-based targeted sequencing using a unique molecular identifier.
    Chung J; Lee KW; Lee C; Shin SH; Kyung S; Jeon HJ; Kim SY; Cho E; Yoo CE; Son DS; Park WY; Park D
    BMC Genomics; 2019 Mar; 20(1):216. PubMed ID: 30871467
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive viral enrichment enables sensitive respiratory virus genomic identification and analysis by next generation sequencing.
    O'Flaherty BM; Li Y; Tao Y; Paden CR; Queen K; Zhang J; Dinwiddie DL; Gross SM; Schroth GP; Tong S
    Genome Res; 2018 Jun; 28(6):869-877. PubMed ID: 29703817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Probe capture enrichment next-generation sequencing of complete foot-and-mouth disease virus genomes in clinical samples.
    Singanallur NB; Anderson DE; Sessions OM; Kamaraj US; Bowden TR; Horsington J; Cowled C; Wang LF; Vosloo W
    J Virol Methods; 2019 Oct; 272():113703. PubMed ID: 31336142
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical validation of targeted next-generation sequencing for inherited disorders.
    Yohe S; Hauge A; Bunjer K; Kemmer T; Bower M; Schomaker M; Onsongo G; Wilson J; Erdmann J; Zhou Y; Deshpande A; Spears MD; Beckman K; Silverstein KA; Thyagarajan B
    Arch Pathol Lab Med; 2015 Feb; 139(2):204-10. PubMed ID: 25611102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. High-Resolution HLA-Typing by Next-Generation Sequencing of Randomly Fragmented Target DNA.
    Wittig M; Juzenas S; Vollstedt M; Franke A
    Methods Mol Biol; 2018; 1802():63-88. PubMed ID: 29858802
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing.
    Baudhuin LM; Lagerstedt SA; Klee EW; Fadra N; Oglesbee D; Ferber MJ
    J Mol Diagn; 2015 Jul; 17(4):456-61. PubMed ID: 25960255
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.
    Robyns T; Kuiperi C; Breckpot J; Devriendt K; Souche E; Van Cleemput J; Willems R; Nuyens D; Matthijs G; Corveleyn A
    Eur J Hum Genet; 2017 Dec; 25(12):1313-1323. PubMed ID: 29255176
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.