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 *

88 related articles for article (PubMed ID: 10723859)

  • 1. New technologies and DNA resources for high throughput biology.
    Spurr N; Darvasi A; Terrett J; Jazwinska L
    Br Med Bull; 1999; 55(2):309-24. PubMed ID: 10723859
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Digital genotyping using molecular affinity and mass spectrometry.
    Kim S; Ruparel HD; Gilliam TC; Ju J
    Nat Rev Genet; 2003 Dec; 4(12):1001-8. PubMed ID: 14631360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SNP and mutation analysis.
    Wang L; Luhm R; Lei M
    Adv Exp Med Biol; 2007; 593():105-16. PubMed ID: 17265721
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA sequencing and genotyping in miniaturized electrophoresis systems.
    Kan CW; Fredlake CP; Doherty EA; Barron AE
    Electrophoresis; 2004 Nov; 25(21-22):3564-88. PubMed ID: 15565709
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Applications of ultra-high-throughput sequencing.
    Fox S; Filichkin S; Mockler TC
    Methods Mol Biol; 2009; 553():79-108. PubMed ID: 19588102
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Using next-generation sequencing approaches to isolate simple sequence repeat (SSR) loci in the plant sciences.
    Zalapa JE; Cuevas H; Zhu H; Steffan S; Senalik D; Zeldin E; McCown B; Harbut R; Simon P
    Am J Bot; 2012 Feb; 99(2):193-208. PubMed ID: 22186186
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Critical review of NGS analyses for de novo genotyping multigene families.
    Lighten J; van Oosterhout C; Bentzen P
    Mol Ecol; 2014 Aug; 23(16):3957-72. PubMed ID: 24954669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SNP genotyping: technologies and biomedical applications.
    Kim S; Misra A
    Annu Rev Biomed Eng; 2007; 9():289-320. PubMed ID: 17391067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preparation of normalized cDNA libraries for 454 Titanium transcriptome sequencing.
    Lai Z; Zou Y; Kane NC; Choi JH; Wang X; Rieseberg LH
    Methods Mol Biol; 2012; 888():119-33. PubMed ID: 22665279
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Next-generation sequencing in childhood disorders.
    Schnekenberg RP; Németh AH
    Arch Dis Child; 2014 Mar; 99(3):284-90. PubMed ID: 24170689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements.
    Parson W; Ballard D; Budowle B; Butler JM; Gettings KB; Gill P; Gusmão L; Hares DR; Irwin JA; King JL; Knijff P; Morling N; Prinz M; Schneider PM; Neste CV; Willuweit S; Phillips C
    Forensic Sci Int Genet; 2016 May; 22():54-63. PubMed ID: 26844919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Generating unigene collections of expressed sequence tag sequences for use in mass spectrometry identification.
    Emmersen J
    Methods Mol Biol; 2007; 367():77-86. PubMed ID: 17185771
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microsatellite DNA capture from enriched libraries.
    Gonzalez EG; Zardoya R
    Methods Mol Biol; 2013; 1006():67-87. PubMed ID: 23546784
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Target enrichment sequencing in cultivated peanut (Arachis hypogaea L.) using probes designed from transcript sequences.
    Peng Z; Fan W; Wang L; Paudel D; Leventini D; Tillman BL; Wang J
    Mol Genet Genomics; 2017 Oct; 292(5):955-965. PubMed ID: 28492983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular engineering approaches for DNA sequencing and analysis.
    Bai X; Edwards J; Ju J
    Expert Rev Mol Diagn; 2005 Sep; 5(5):797-808. PubMed ID: 16149881
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new MALDI-TOF based mini-sequencing assay for genotyping of SNPS.
    Sun X; Ding H; Hung K; Guo B
    Nucleic Acids Res; 2000 Jun; 28(12):E68. PubMed ID: 10871391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Large scale DNA sequencing: new challenges emerge--the 2007 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2008 May; 29(5):765-8. PubMed ID: 18348287
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A glimpse into past, present, and future DNA sequencing.
    Morey M; Fernández-Marmiesse A; Castiñeiras D; Fraga JM; Couce ML; Cocho JA
    Mol Genet Metab; 2013; 110(1-2):3-24. PubMed ID: 23742747
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo assembly and genomic structural variation analysis with genome sequencer FLX 3K long-tag paired end reads.
    Jarvie T; Harkins T
    Biotechniques; 2008 May; 44(6):829-31. PubMed ID: 18476839
    [No Abstract]   [Full Text] [Related]  

  • 20. An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data.
    Jun G; Wing MK; Abecasis GR; Kang HM
    Genome Res; 2015 Jun; 25(6):918-25. PubMed ID: 25883319
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.