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ARTICLES

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  Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA.

  • M Lagerström,
  • J Parik,
  • H Malmgren,
  • J Stewart,
  • U Pettersson,
  • and U Landegren

  Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111
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  Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase.

  • P E Nisson,
  • A Rashtchian,
  • and P C Watkins

  Genome Res. November 1991 1: 120-123; doi:10.1101/gr.1.2.120
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  OSP: a computer program for choosing PCR and DNA sequencing primers.

  • L Hillier and
  • P Green

  Genome Res. November 1991 1: 124-128; doi:10.1101/gr.1.2.124
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  Use of a simplified single-site PCR to facilitate cloning of genomic DNA sequences flanking a transgene integration site.

  • G R MacGregor and
  • P A Overbeek

  Genome Res. November 1991 1: 129-135; doi:10.1101/gr.1.2.129
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  Generation of competitor DNA fragments for quantitative PCR.

  • K Uberla,
  • C Platzer,
  • T Diamantstein,
  • and T Blankenstein

  Genome Res. November 1991 1: 136-139; doi:10.1101/gr.1.2.136
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• Rapid and reliable cloning of PCR products.

  • J B Lorens

  Genome Res. November 1991 1: 140-141; doi:10.1101/gr.1.2.140
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• Slow inactivation of dry PCR templates by UV light.

  • M R Fairfax,
  • M A Metcalf,
  • and R W Cone

  Genome Res. November 1991 1: 142-143; doi:10.1101/gr.1.2.142
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• A simple and rapid method to analyze specific mRNAs from few cells in a semi-quantitative way using the polymerase chain reaction.

  • J Golay,
  • F Passerini,
  • and M Introna

  Genome Res. November 1991 1: 144-145; doi:10.1101/gr.1.2.144
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• Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA)

  • D R Jacobson and
  • T Moskovits

  Genome Res. November 1991 1: 146-148; doi:10.1101/gr.1.2.146
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