Connection

RICHARD GIBBS to Polymerase Chain Reaction

This is a "connection" page, showing publications RICHARD GIBBS has written about Polymerase Chain Reaction.
Connection Strength

1.169
  1. Validation of Single-Nucleotide Mosaic Variants Through Droplet Digital PCR. Curr Protoc. 2024 May; 4(5):e1041.
    View in: PubMed
    Score: 0.167
  2. Improved ligation-anchored PCR strategy for identification of 5' ends of transcripts. Biotechniques. 1996 Jul; 21(1):34-6, 38.
    View in: PubMed
    Score: 0.097
  3. Multiplex PCR: advantages, development, and applications. PCR Methods Appl. 1994 Feb; 3(4):S65-75.
    View in: PubMed
    Score: 0.082
  4. Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products. PCR Methods Appl. 1993 May; 2(4):293-300.
    View in: PubMed
    Score: 0.078
  5. Polymerase chain reaction techniques. Curr Opin Biotechnol. 1991 Feb; 2(1):69-75.
    View in: PubMed
    Score: 0.067
  6. DNA amplification by the polymerase chain reaction. Anal Chem. 1990 Jul 01; 62(13):1202-14.
    View in: PubMed
    Score: 0.064
  7. The use of primers from highly conserved pol regions to identify uncharacterized retroviruses by the polymerase chain reaction. J Virol Methods. 1990 Apr; 28(1):33-46.
    View in: PubMed
    Score: 0.063
  8. Direct selection of human genomic loci by microarray hybridization. Nat Methods. 2007 Nov; 4(11):903-5.
    View in: PubMed
    Score: 0.053
  9. The genomic organization of Isopeptidase T-3 (ISOT-3), a new member of the ubiquitin specific protease family (UBP). Gene. 1998 Sep 14; 217(1-2):101-6.
    View in: PubMed
    Score: 0.028
  10. Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination. Genome Res. 1997 Mar; 7(3):268-80.
    View in: PubMed
    Score: 0.025
  11. Molecular and phenotypic variation in patients with severe Hunter syndrome. Hum Mol Genet. 1997 Mar; 6(3):479-86.
    View in: PubMed
    Score: 0.025
  12. Method for 96-well M13 DNA template preparations for large-scale sequencing. Biotechniques. 1996 Jun; 20(6):1022-7.
    View in: PubMed
    Score: 0.024
  13. A "double adaptor" method for improved shotgun library construction. Anal Biochem. 1996 Apr 05; 236(1):107-13.
    View in: PubMed
    Score: 0.024
  14. Analysis of human immunodeficiency virus type 1 integrase mutants. Virology. 1995 Aug 01; 211(1):332-5.
    View in: PubMed
    Score: 0.023
  15. 130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus. Genome Res. 1995 Aug; 5(1):71-8.
    View in: PubMed
    Score: 0.023
  16. Accurate determination of DNA in agarose gels using the novel algorithm GelScann(1.0). Comput Appl Biosci. 1995 Apr; 11(2):187-94.
    View in: PubMed
    Score: 0.022
  17. Analysis of HIV type 1 reverse transcriptase expression in a human cell line. AIDS Res Hum Retroviruses. 1994 Sep; 10(9):1117-24.
    View in: PubMed
    Score: 0.021
  18. Adaptor-based uracil DNA glycosylase cloning simplifies shotgun library construction for large-scale sequencing. Anal Biochem. 1994 May 01; 218(2):300-8.
    View in: PubMed
    Score: 0.021
  19. Multiplex DNA amplification and solid-phase direct sequencing for mutation analysis at the hprt locus in Chinese hamster cells. Mutat Res. 1993 Aug; 288(2):237-48.
    View in: PubMed
    Score: 0.020
  20. A human dimorphism resulting from loss of an Alu. Genomics. 1992 Nov; 14(3):590-7.
    View in: PubMed
    Score: 0.019
  21. Genomic sequencing of key genes in mouse pancreatic cancer cells. Curr Mol Med. 2012 Mar; 12(3):331-41.
    View in: PubMed
    Score: 0.018
  22. A simple protocol for the automation of DNA cycle sequencing reactions and polymerase chain reactions. DNA Seq. 1992; 3(1):17-23.
    View in: PubMed
    Score: 0.018
  23. Polymerase chain reaction-based comprehensive procedure for the analysis of the mutation spectrum at the hypoxanthine-guanine phosphoribosyltransferase locus in Chinese hamster cells. Environ Mol Mutagen. 1992; 19(4):267-73.
    View in: PubMed
    Score: 0.018
  24. Evolution of human immunodeficiency virus type 1 nucleotide sequence diversity among close contacts. Proc Natl Acad Sci U S A. 1991 Dec 15; 88(24):11236-40.
    View in: PubMed
    Score: 0.018
  25. The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNA. Gene. 1991 Dec 15; 108(2):299-304.
    View in: PubMed
    Score: 0.018
  26. Pentanucleotide repeat length polymorphism at the human CD4 locus. Nucleic Acids Res. 1991 Sep 11; 19(17):4791.
    View in: PubMed
    Score: 0.017
  27. Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus. Proc Natl Acad Sci U S A. 1991 Jul 15; 88(14):6157-61.
    View in: PubMed
    Score: 0.017
  28. Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families. Genomics. 1990 Jun; 7(2):235-44.
    View in: PubMed
    Score: 0.016
  29. PCR test for cystic fibrosis deletion. Nature. 1990 Jan 18; 343(6255):220.
    View in: PubMed
    Score: 0.016
  30. Sequencing the full-length of the phosphatase and tensin homolog (PTEN) gene in hepatocellular carcinoma (HCC) using the 454 GS20 and Illumina GA DNA sequencing platforms. World J Surg. 2009 Apr; 33(4):647-52.
    View in: PubMed
    Score: 0.015
  31. Mutation survey of known LCA genes and loci in the Saudi Arabian population. Invest Ophthalmol Vis Sci. 2009 Mar; 50(3):1336-43.
    View in: PubMed
    Score: 0.014
  32. Novel potential ALL low-risk markers revealed by gene expression profiling with new high-throughput SSH-CCS-PCR. Leukemia. 2003 Sep; 17(9):1891-900.
    View in: PubMed
    Score: 0.010
  33. Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity. Genome Res. 1997 Jun; 7(6):642-8.
    View in: PubMed
    Score: 0.006
  34. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nat Genet. 1996 May; 13(1):109-13.
    View in: PubMed
    Score: 0.006
  35. Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient. Hum Mol Genet. 1992 Nov; 1(8):645-6.
    View in: PubMed
    Score: 0.005
  36. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet. 1991 Nov; 49(5):951-60.
    View in: PubMed
    Score: 0.004
  37. Fidelity of targeted recombination in human fibroblasts and murine embryonic stem cells. Proc Natl Acad Sci U S A. 1991 Sep 15; 88(18):8067-71.
    View in: PubMed
    Score: 0.004
  38. Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome. Trans Assoc Am Physicians. 1989; 102:185-94.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.