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 *

105 related articles for article (PubMed ID: 28120836)

  • 1. From exomes to genomes: challenges and solutions in population-based genetic association studies.
    Auer PL; Leal SM
    Eur J Hum Genet; 2017 Apr; 25(4):395-396. PubMed ID: 28120836
    [No Abstract]   [Full Text] [Related]  

  • 2. Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.
    Richardson R; Sowden J; Gerth-Kahlert C; Moore AT; Moosajee M
    Eur J Hum Genet; 2017 Apr; 25(4):. PubMed ID: 28098148
    [No Abstract]   [Full Text] [Related]  

  • 3. Genome-Wide Copy Number Alteration Detection in Preimplantation Genetic Diagnosis.
    Deleye L; De Coninck D; Deforce D; Van Nieuwerburgh F
    Methods Mol Biol; 2018; 1712():27-42. PubMed ID: 29224066
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Applications of the 1000 Genomes Project resources.
    Zheng-Bradley X; Flicek P
    Brief Funct Genomics; 2017 May; 16(3):163-170. PubMed ID: 27436001
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enabling genome-wide association testing with multiple diseases and no healthy controls.
    Tom J; Chang D; Wuster A; Mukhyala K; Cuenco K; Cowgill A; Vogel J; Reeder J; Yaspan B; Hunkapiller J; Brauer M; Behrens T; Forrest W; Bhangale T
    Gene; 2019 Feb; 684():118-123. PubMed ID: 30366082
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Population-specific genetic variation in large sequencing data sets: why more data is still better.
    van Rooij JGJ; Jhamai M; Arp PP; Nouwens SCA; Verkerk M; Hofman A; Ikram MA; Verkerk AJ; van Meurs JBJ; Rivadeneira F; Uitterlinden AG; Kraaij R
    Eur J Hum Genet; 2017 Oct; 25(10):1173-1175. PubMed ID: 28905877
    [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. Rapid and affordable genome-wide bisulfite DNA sequencing by XmaI-reduced representation bisulfite sequencing.
    Tanas AS; Borisova ME; Kuznetsova EB; Rudenko VV; Karandasheva KO; Nemtsova MV; Izhevskaya VL; Simonova OA; Larin SS; Zaletaev DV; Strelnikov VV
    Epigenomics; 2017 Jun; 9(6):833-847. PubMed ID: 28488887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
    Kornilov SA; Rakhlin N; Koposov R; Lee M; Yrigollen C; Caglayan AO; Magnuson JS; Mane S; Chang JT; Grigorenko EL
    Pediatrics; 2016 Apr; 137(4):. PubMed ID: 27016271
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.
    Qiao D; Lange C; Beaty TH; Crapo JD; Barnes KC; Bamshad M; Hersh CP; Morrow J; Pinto-Plata VM; Marchetti N; Bueno R; Celli BR; Criner GJ; Silverman EK; Cho MH; ; ;
    Am J Respir Crit Care Med; 2016 Jun; 193(12):1353-63. PubMed ID: 26736064
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Accurate whole genome sequencing as the ultimate genetic test.
    Drmanac R; Peters BA; Church GM; Reid CA; Xu X
    Clin Chem; 2015 Jan; 61(1):305-6. PubMed ID: 25479756
    [No Abstract]   [Full Text] [Related]  

  • 12. Baby genome screening: paving the way to genetic discrimination?
    Seidel MG
    BMJ; 2017 Jul; 358():j3294. PubMed ID: 28729238
    [No Abstract]   [Full Text] [Related]  

  • 13. Reference genotype and exome data from an Australian Aboriginal population for health-based research.
    Tang D; Anderson D; Francis RW; Syn G; Jamieson SE; Lassmann T; Blackwell JM
    Sci Data; 2016 Apr; 3():160023. PubMed ID: 27070114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A New Reference Genome Assembly for the Microcrustacean
    Ye Z; Xu S; Spitze K; Asselman J; Jiang X; Ackerman MS; Lopez J; Harker B; Raborn RT; Thomas WK; Ramsdell J; Pfrender ME; Lynch M
    G3 (Bethesda); 2017 May; 7(5):1405-1416. PubMed ID: 28235826
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.
    Smith LD; Willig LK; Kingsmore SF
    Cold Spring Harb Perspect Med; 2015 Dec; 6(2):a023168. PubMed ID: 26684335
    [TBL] [Abstract][Full Text] [Related]  

  • 16. From genome-wide association studies to next-generation sequencing: lessons from the past and planning for the future.
    Sharma M; Krüger R; Gasser T
    JAMA Neurol; 2014 Jan; 71(1):5-6. PubMed ID: 24190229
    [No Abstract]   [Full Text] [Related]  

  • 17. From Pine Cones to Read Clouds: Rescaffolding the Megagenome of Sugar Pine (
    Crepeau MW; Langley CH; Stevens KA
    G3 (Bethesda); 2017 May; 7(5):1563-1568. PubMed ID: 28341701
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide significance testing of variation from single case exomes.
    Wilfert AB; Chao KR; Kaushal M; Jain S; Zöllner S; Adams DR; Conrad DF
    Nat Genet; 2016 Dec; 48(12):1455-1461. PubMed ID: 27776118
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of copy number variation in French dairy and beef breeds using next-generation sequencing.
    Letaief R; Rebours E; Grohs C; Meersseman C; Fritz S; Trouilh L; Esquerré D; Barbieri J; Klopp C; Philippe R; Blanquet V; Boichard D; Rocha D; Boussaha M
    Genet Sel Evol; 2017 Oct; 49(1):77. PubMed ID: 29065859
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Findings in genome-wide association studies on asthma lack generalisation.
    Zhang G; Goldblatt J; Lesouëf P
    Clin Respir J; 2010 Oct; 4(4):e8-9. PubMed ID: 20887339
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.