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 *

164 related articles for article (PubMed ID: 32105409)

  • 1. An Overview of Molecular Genetic Diagnosis Techniques.
    Goswami RS; Harada S
    Curr Protoc Hum Genet; 2020 Mar; 105(1):e97. PubMed ID: 32105409
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Massively parallel sequencing on human cleavage-stage embryos to detect chromosomal abnormality.
    Zhou Z; Ma Y; Li Q; Zhang Y; Huang Y; Tu Z; Ma N; Li M; Wang J; Li J; Lu W
    Eur J Med Genet; 2018 Jan; 61(1):34-42. PubMed ID: 29032163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing.
    Palculict ME; Zhang VW; Wong LJ; Wang J
    Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next-generation sequencing and its applications in molecular diagnostics.
    Su Z; Ning B; Fang H; Hong H; Perkins R; Tong W; Shi L
    Expert Rev Mol Diagn; 2011 Apr; 11(3):333-43. PubMed ID: 21463242
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls.
    McInerney-Leo AM; Duncan EL
    Front Endocrinol (Lausanne); 2020; 11():628946. PubMed ID: 33679611
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Towards a national standardisation of NGS studies in the diagnosis of myopathies].
    Krahn M; Cerino M; Campana-Salort E; Cossée M
    Med Sci (Paris); 2017 Nov; 33 Hors série n°1():30-33. PubMed ID: 29139383
    [No Abstract]   [Full Text] [Related]  

  • 7. Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.
    Dong Z; Ye L; Yang Z; Chen H; Yuan J; Wang H; Guo X; Li Y; Wang J; Chen F; Cheung SW; Morton CC; Jiang H; Choy KW
    Curr Protoc Hum Genet; 2018 Jan; 96():8.18.1-8.18.16. PubMed ID: 29364520
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [New technologies for the human genome exploration].
    Keren B; Schluth-Bolard C; Egea G; Sanlaville D
    Arch Pediatr; 2010 Nov; 17(11):1605-8. PubMed ID: 20843672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Validation of a next-generation sequencing assay for clinical molecular oncology.
    Cottrell CE; Al-Kateb H; Bredemeyer AJ; Duncavage EJ; Spencer DH; Abel HJ; Lockwood CM; Hagemann IS; O'Guin SM; Burcea LC; Sawyer CS; Oschwald DM; Stratman JL; Sher DA; Johnson MR; Brown JT; Cliften PF; George B; McIntosh LD; Shrivastava S; Nguyen TT; Payton JE; Watson MA; Crosby SD; Head RD; Mitra RD; Nagarajan R; Kulkarni S; Seibert K; Virgin HW; Milbrandt J; Pfeifer JD
    J Mol Diagn; 2014 Jan; 16(1):89-105. PubMed ID: 24211365
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
    Zhu X; Li J; Ru T; Wang Y; Xu Y; Yang Y; Wu X; Cram DS; Hu Y
    Prenat Diagn; 2016 Apr; 36(4):321-7. PubMed ID: 26833920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Introducing WISECONDOR for noninvasive prenatal diagnostics.
    Straver R; Sistermans EA; Reinders MJ
    Expert Rev Mol Diagn; 2014 Jun; 14(5):513-5. PubMed ID: 24831532
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next generation molecular diagnosis of mitochondrial disorders.
    Wong LJ
    Mitochondrion; 2013 Jul; 13(4):379-87. PubMed ID: 23473862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Next-generation sequencing applied to molecular diagnostics.
    Natrajan R; Reis-Filho JS
    Expert Rev Mol Diagn; 2011 May; 11(4):425-44. PubMed ID: 21545259
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.
    Lin X; Tang W; Ahmad S; Lu J; Colby CC; Zhu J; Yu Q
    Hear Res; 2012 Jun; 288(1-2):67-76. PubMed ID: 22269275
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of Genetic Rearrangements in the Regulators of Complement Activation RCA Cluster by High-Throughput Sequencing and MLPA.
    García-Fernández J; Vilches-Arroyo S; Olavarrieta L; Pérez-Pérez J; Rodríguez de Córdoba S
    Methods Mol Biol; 2021; 2227():159-178. PubMed ID: 33847941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.
    Dong Z; Jiang L; Yang C; Hu H; Wang X; Chen H; Choy KW; Hu H; Dong Y; Hu B; Xu J; Long Y; Cao S; Chen H; Wang WJ; Jiang H; Xu F; Yao H; Xu X; Liang Z
    Hum Mutat; 2014 May; 35(5):625-36. PubMed ID: 24610732
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
    Hu P; Qiao F; Wang Y; Meng L; Ji X; Luo C; Xu T; Zhou R; Zhang J; Yu B; Wang L; Wang T; Pan Q; Ma D; Liang D; Xu Z
    Ultrasound Obstet Gynecol; 2018 Aug; 52(2):205-211. PubMed ID: 29536580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.
    Hochstenbach R; van Binsbergen E; Schuring-Blom H; Buijs A; Ploos van Amstel HK
    Eur J Med Genet; 2019 Sep; 62(9):103543. PubMed ID: 30248410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detecting rare variants for psychiatric disorders using next generation sequencing: a methods primer.
    Altmann A; Quast C; Weber P
    Curr Psychiatry Rep; 2013 Jan; 15(1):333. PubMed ID: 23250814
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Next-generation sequencing analysis of lung and colon carcinomas reveals a variety of genetic alterations.
    Chevrier S; Arnould L; Ghiringhelli F; Coudert B; Fumoleau P; Boidot R
    Int J Oncol; 2014 Sep; 45(3):1167-74. PubMed ID: 24990411
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.