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 *

76 related articles for article (PubMed ID: 21697130)

  • 21. Genotype calling in tetraploid species from bi-allelic marker data using mixture models.
    Voorrips RE; Gort G; Vosman B
    BMC Bioinformatics; 2011 May; 12():172. PubMed ID: 21595880
    [TBL] [Abstract][Full Text] [Related]  

  • 22. High-throughput genotyping with single nucleotide polymorphisms.
    Ranade K; Chang MS; Ting CT; Pei D; Hsiao CF; Olivier M; Pesich R; Hebert J; Chen YD; Dzau VJ; Curb D; Olshen R; Risch N; Cox DR; Botstein D
    Genome Res; 2001 Jul; 11(7):1262-8. PubMed ID: 11435409
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Refinement of single-nucleotide polymorphism genotyping methods on human genomic DNA: amplifluor allele-specific polymerase chain reaction versus ligation detection reaction-TaqMan.
    Rickert AM; Borodina TA; Kuhn EJ; Lehrach H; Sperling S
    Anal Biochem; 2004 Jul; 330(2):288-97. PubMed ID: 15203335
    [TBL] [Abstract][Full Text] [Related]  

  • 24. LinkImputeR: user-guided genotype calling and imputation for non-model organisms.
    Money D; Migicovsky Z; Gardner K; Myles S
    BMC Genomics; 2017 Jul; 18(1):523. PubMed ID: 28693460
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Discrimination of SNPs in GC-rich regions using a modified hydrolysis probe chemistry protocol.
    Mowjoodi A; Paton TA; Scherer SW
    Biotechniques; 2014 Dec; 57(6):313-6. PubMed ID: 25495732
    [TBL] [Abstract][Full Text] [Related]  

  • 26. ACCUSA--accurate SNP calling on draft genomes.
    Fröhler S; Dieterich C
    Bioinformatics; 2010 May; 26(10):1364-5. PubMed ID: 20363730
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Enhanced discrimination of single nucleotide polymorphism in genotyping by phosphorothioate proofreading allele-specific amplification.
    Hu YJ; Li ZF; Diamond AM
    Anal Biochem; 2007 Oct; 369(1):54-9. PubMed ID: 17631854
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Design of an allele-specific PCR assay to genotype the rs12255372 SNP in a pilot study of association between common TCF7L2 polymorphisms and type 2 diabetes in Venezuelans.
    Moran Y; Labrador L; Camargo ME; Fernández D; Chiurillo MA
    Arch Endocrinol Metab; 2015 Jul; 60(3):246-51. PubMed ID: 26201011
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Comparison of high-resolution melting analysis, TaqMan Allelic discrimination assay, and sanger sequencing for Clopidogrel efficacy genotyping in routine molecular diagnostics.
    Zhang L; Cui G; Li Z; Wang H; Ding H; Wang DW
    J Mol Diagn; 2013 Sep; 15(5):600-6. PubMed ID: 23810503
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Characteristic and influencing factors of Taqman genotyping calling error.
    Yu S; Li X; Liu X; Wang Y; Yu F; Xue Y; Mao Z; Wang C; Li W
    J Clin Lab Anal; 2018 Nov; 32(9):e22613. PubMed ID: 29943492
    [TBL] [Abstract][Full Text] [Related]  

  • 31. SNP genotyping using KASPar assays.
    Smith SM; Maughan PJ
    Methods Mol Biol; 2015; 1245():243-56. PubMed ID: 25373762
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Simple SNP-based minimal marker genotyping for Humulus lupulus L. identification and variety validation.
    Henning JA; Coggins J; Peterson M
    BMC Res Notes; 2015 Oct; 8():542. PubMed ID: 26438052
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data.
    Burkett KM; McNeney B; Graham J
    Bioinformatics; 2016 May; 32(10):1580-2. PubMed ID: 26787665
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Whole Blood PCR Amplification with Pfu DNA Polymerase and Its Application in Single-Nucleotide Polymorphism Analysis.
    Liu EP; Wang Y; He XH; Guan JJ; Wang J; Qin ZH; Sun WP
    Genet Test Mol Biomarkers; 2015 Nov; 19(11):610-6. PubMed ID: 26360116
    [TBL] [Abstract][Full Text] [Related]  

  • 35. High-throughput SNP genotyping by single-tube PCR with Tm-shift primers.
    Wang J; Chuang K; Ahluwalia M; Patel S; Umblas N; Mirel D; Higuchi R; Germer S
    Biotechniques; 2005 Dec; 39(6):885-93. PubMed ID: 16382908
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y; Segal MR; Yang YH; Yeh RF
    Bioinformatics; 2007 Jun; 23(12):1459-67. PubMed ID: 17459966
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Homogeneous scoring of single-nucleotide polymorphisms: comparison of the 5'-nuclease TaqMan assay and Molecular Beacon probes.
    Täpp I; Malmberg L; Rennel E; Wik M; Syvänen AC
    Biotechniques; 2000 Apr; 28(4):732-8. PubMed ID: 10769752
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two-temperature LATE-PCR endpoint genotyping.
    Sanchez JA; Abramowitz JD; Salk JJ; Reis AH; Rice JE; Pierce KE; Wangh LJ
    BMC Biotechnol; 2006 Dec; 6():44. PubMed ID: 17144924
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Algorithm for the Automated Evaluation of NAT2 Genotypes.
    Michael G; Thier R; Blaszkewicz M; Selinski S; Golka K
    Methods Mol Biol; 2018; 1655():77-96. PubMed ID: 28889379
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Development of a rapid clinical TPMT genotyping assay.
    Burchard PR; Abou Tayoun AN; Lefferts JA; Lewis LD; Tsongalis GJ; Cervinski MA
    Clin Biochem; 2014 Oct; 47(15):126-9. PubMed ID: 25093923
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.