BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

442 related articles for article (PubMed ID: 26508566)

  • 1. Guidelines for diagnostic next-generation sequencing.
    Matthijs G; Souche E; Alders M; Corveleyn A; Eck S; Feenstra I; Race V; Sistermans E; Sturm M; Weiss M; Yntema H; Bakker E; Scheffer H; Bauer P; ;
    Eur J Hum Genet; 2016 Jan; 24(1):2-5. PubMed ID: 26508566
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing.
    Matthijs G; Dierking A; Schmidtke J
    Eur J Hum Genet; 2016 Jan; 24(1):1. PubMed ID: 26508569
    [No Abstract]   [Full Text] [Related]  

  • 3. Review of Clinical Next-Generation Sequencing.
    Yohe S; Thyagarajan B
    Arch Pathol Lab Med; 2017 Nov; 141(11):1544-1557. PubMed ID: 28782984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.
    Vrijenhoek T; Kraaijeveld K; Elferink M; de Ligt J; Kranendonk E; Santen G; Nijman IJ; Butler D; Claes G; Costessi A; Dorlijn W; van Eyndhoven W; Halley DJ; van den Hout MC; van Hove S; Johansson LF; Jongbloed JD; Kamps R; Kockx CE; de Koning B; Kriek M; Lekanne Dit Deprez R; Lunstroo H; Mannens M; Mook OR; Nelen M; Ploem C; Rijnen M; Saris JJ; Sinke R; Sistermans E; van Slegtenhorst M; Sleutels F; van der Stoep N; van Tienhoven M; Vermaat M; Vogel M; Waisfisz Q; Marjan Weiss J; van den Wijngaard A; van Workum W; Ijntema H; van der Zwaag B; van IJcken WF; den Dunnen J; Veltman JA; Hennekam R; Cuppen E
    Eur J Hum Genet; 2015 Sep; 23(9):1142-50. PubMed ID: 25626705
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted next-generation sequencing panels for monogenetic disorders in clinical diagnostics: the opportunities and challenges.
    de Koning TJ; Jongbloed JD; Sikkema-Raddatz B; Sinke RJ
    Expert Rev Mol Diagn; 2015 Jan; 15(1):61-70. PubMed ID: 25367078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CCMG practice guideline: laboratory guidelines for next-generation sequencing.
    Hume S; Nelson TN; Speevak M; McCready E; Agatep R; Feilotter H; Parboosingh J; Stavropoulos DJ; Taylor S; Stockley TL;
    J Med Genet; 2019 Dec; 56(12):792-800. PubMed ID: 31300550
    [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. Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories.
    Weiss MM; Van der Zwaag B; Jongbloed JD; Vogel MJ; Brüggenwirth HT; Lekanne Deprez RH; Mook O; Ruivenkamp CA; van Slegtenhorst MA; van den Wijngaard A; Waisfisz Q; Nelen MR; van der Stoep N
    Hum Mutat; 2013 Oct; 34(10):1313-21. PubMed ID: 23776008
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited Diseases.
    Santani A; Murrell J; Funke B; Yu Z; Hegde M; Mao R; Ferreira-Gonzalez A; Voelkerding KV; Weck KE
    Arch Pathol Lab Med; 2017 Jun; 141(6):787-797. PubMed ID: 28322587
    [TBL] [Abstract][Full Text] [Related]  

  • 10. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
    Aziz N; Zhao Q; Bry L; Driscoll DK; Funke B; Gibson JS; Grody WW; Hegde MR; Hoeltge GA; Leonard DG; Merker JD; Nagarajan R; Palicki LA; Robetorye RS; Schrijver I; Weck KE; Voelkerding KV
    Arch Pathol Lab Med; 2015 Apr; 139(4):481-93. PubMed ID: 25152313
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing].
    Wang J; Gu W; Huang H; Shen Y; Xiong H; Huang Y; Qi M; An D; Ma D; Deng X; Gao Y; Wang X; Zhou Z; Wu J; Xu X; Zhang W; Kang H; Peng Z; Yu S; Wang L; Huang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):334-338. PubMed ID: 32128754
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Guidelines for cytogenetic investigations in tumours.
    Hastings RJ; Bown N; Tibiletti MG; Debiec-Rychter M; Vanni R; Espinet B; van Roy N; Roberts P; van den Berg-de-Ruiter E; Bernheim A; Schoumans J; Chatters S; Zemanova Z; Stevens-Kroef M; Simons A; Heim S; Salido M; Ylstra B; Betts DR; ;
    Eur J Hum Genet; 2016 Jan; 24(1):6-13. PubMed ID: 25804401
    [No Abstract]   [Full Text] [Related]  

  • 14. [A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (3) - Data analysis].
    Sun J; Huang Y; Wang X; Li W; An D; Gao Y; Xiong H; Zhou Z; Xu X; Deng X; Wang X; Huang H; Peng Z; Zhang W; Yu S; Wang L; Gu W; Huang S; Shen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):345-351. PubMed ID: 32128756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical utility in infants with suspected monogenic conditions through next-generation sequencing.
    Hong S; Wang L; Zhao D; Zhang Y; Chen Y; Tan J; Liang L; Zhu T
    Mol Genet Genomic Med; 2019 Jun; 7(6):e684. PubMed ID: 30968598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (4) - Report interpretation and genetic counseling].
    Huang H; Shen Y; Gu W; Huang Y; Wang X; Gao Y; Xiong H; Zhou Z; Wu J; Ma D; An D; Zhang W; Fu Q; Xiong X; Peng Z; Wang L; Huang S; Qi M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):352-357. PubMed ID: 32128757
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of Disease Susceptibility Alleles in the Next Generation Sequencing Era.
    DiStefano JK; Kingsley CB
    Methods Mol Biol; 2018; 1706():3-16. PubMed ID: 29423790
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recommendations for whole genome sequencing in diagnostics for rare diseases.
    Souche E; Beltran S; Brosens E; Belmont JW; Fossum M; Riess O; Gilissen C; Ardeshirdavani A; Houge G; van Gijn M; Clayton-Smith J; Synofzik M; de Leeuw N; Deans ZC; Dincer Y; Eck SH; van der Crabben S; Balasubramanian M; Graessner H; Sturm M; Firth H; Ferlini A; Nabbout R; De Baere E; Liehr T; Macek M; Matthijs G; Scheffer H; Bauer P; Yntema HG; Weiss MM
    Eur J Hum Genet; 2022 Sep; 30(9):1017-1021. PubMed ID: 35577938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assuring the Quality of Next-Generation Sequencing in Clinical Microbiology and Public Health Laboratories.
    Gargis AS; Kalman L; Lubin IM
    J Clin Microbiol; 2016 Dec; 54(12):2857-2865. PubMed ID: 27510831
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical application of next-generation sequencing for Mendelian diseases.
    Jamuar SS; Tan EC
    Hum Genomics; 2015 Jun; 9(1):10. PubMed ID: 26076878
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.