Searching journal content for articles similar to McClelland and Welsh 4 (1): S66.

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  1. REVIEW: DNA fingerprinting by arbitrarily primed PCR.
    • M McClelland and
    • J Welsh
    Genome Res. August 1994 4: S59-S65
    ...amplified polymorphic DNA (RAPD) analysis. In Methods in plant molecular biology and technology (ed. B.R. Glick and J.E. Thompson). CRC Press, Inc., Boca Rotan, Fl, USA; London, U.K. 8.. McClelland, M. , Welsh. J. McClelland, M. and Welsh. J. 1994 . RNA fingerprinting by arbitrarily primed PCR. PCR Methods...
  2. ARTICLE: DNA fingerprinting of crude bacterial lysates using degenerate RAPD primers.
    • S A Sakallah,
    • R W Lanning,
    • and D L Cooper
    Genome Res. April 1995 4: 265-268
    ....-G. Sonntag, and M.V.K. Doeberitz. 1994. Characteriza- tion of contaminating DNA in Taq poly- merase which occurs during amplifica- tion with a primer set for legionella 5S ribosomal RNA. Mol. Cell. Probes 8: 11-14. Received January 9, 1995; accepted in revised form February 15, 1995. 268 PCR Methods...
  3. ARTICLES: Detection and differential display of expressed genes by DDRT-PCR.
    • D Bauer,
    • P Warthoe,
    • M Rohde,
    • and M Strauss
    Genome Res. October 1994 4: S97-S108
    ..., J., , Chada, K. , Dalai, S.S. , Cheng, R. , Ralph, D. , McClelland. M. Welsh, J., Chada, K. Dalai, S.S. Cheng, R. Ralph, D. and McClelland. M. 1992 . Arbitrarily primed PCR fingerprinting of RNA. Nucleic Acids Res. 20 : 4965 – 4970 . 7.. Bauer, D., , M‡ller, H. , Reich, J. , Ahrenkiel, V. , Warthoe...
  4. ARTICLES: Ligation-mediated PCR of restriction fragments from large DNA molecules.
    • D R Smith
    Genome Res. August 1992 2: 21-27; doi:10.1101/gr.2.1.21
    ...of small amounts of undefined RNA. Gene 81 : 295 – 306 . 16.. Timblin, C., , Battey, J. , Kuehl. W.M. Timblin, C., Battey, J. and Kuehl. W.M. 1990 . Application for PCR technology to subtractive cDNA cloning: Identification of genes expressed specifically in murine plasmacytoma cells. Nucleic Acids Res. 18...
  5. ARTICLE: Effect of PCR conditions on the formation of heteroduplex and single-stranded DNA products in the amplification of bacterial ribosomal DNA spacer regions.
    • M A Jensen and
    • N Straus
    Genome Res. December 1993 3: 186-194
    ...of the spacer regions be- tween the 16S and 23S rRNA genetic loci PCR Methods and Applications 187 tRNA Hy~rvariable Spac~ Regions FIGURE 1 Schematic representation f an rRNA operon showing the approximate priming sites for the PCR amplification ofthe 16S/23S spacer egion. The number of tRNA genes...
  6. Research: Divergence patterns of genic copy number variation in natural populations of the house mouse (Mus musculus domesticus) reveal three conserved genes with major population-specific expansions
    • Željka Pezer,
    • Bettina Harr,
    • Meike Teschke,
    • Hiba Babiker,
    • and Diethard Tautz
    Genome Res. August 2015 25: 1114-1124; Published in Advance July 6, 2015, doi:10.1101/gr.187187.114
    ...to a nonredundant list of coordinates that corresponded to 26,756 unique transcription units (defined by transcription start and end sites).Droplet digital PCR validationTo validate the CNVs detected by CNVnator, PrimeTime qPCR assays (Integrated DNA Technologies) were used in duplex reactions to measure the copy...
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  7. Method: Identification of the shortest species-specific oligonucleotide sequences
    • Ioannis Mouratidis,
    • Maxwell A. Konnaris,
    • Nikol Chantzi,
    • Candace S.Y. Chan,
    • Michail Patsakis,
    • Kimonas Provatas,
    • Austin Montgomery,
    • Fotis A. Baltoumas,
    • Congzhou M. Sha,
    • Manvita Mareboina,
    • Georgios A. Pavlopoulos,
    • Dionysios V. Chartoumpekis,
    • and Ilias Georgakopoulos-Soares
    Genome Res. February 2025 35: 279-295; Published in Advance January 2, 2025, doi:10.1101/gr.280070.124
    ...al. 2021b) and have biological significance. Additionally, primes could serve practical purposes, such as PCR primers, highly specific platforms in CRISPR construct designs, genomic barcodes, and sample labeling. Previous studies examined a limited number of s and derived 60,370 15 bp nucleic prime...
    OPEN ACCESS ARTICLE
  8. LETTER: Characterization of Nonfunctional V1R-like Pheromone Receptor Sequences in Human
    • Dominique Giorgi,
    • Cynthia Friedman,
    • Barbara J. Trask,
    • and Sylvie Rouquier
    Genome Res. December 1, 2000 10: 1979-1985; doi:10.1101/gr.146700
    ...; Rouquier et al. 1998 ). The seven rat V1Rs form one family, which is divided into three subfamilies. The two human sequences assort into two subfamilies of a second family. To identify any additional V1R-like sequences among the 46 clones that were generated with the degenerate-primed PCR but not sequenced...
  9. RESEARCH: Strategies for Mutational Analysis of the Large Multiexon ATM Gene Using High-Density Oligonucleotide Arrays
    • Joseph G. Hacia,
    • Bryan Sun,
    • Nathaniel Hunt,
    • Keith Edgemon,
    • Deborah Mosbrook,
    • Christiane Robbins,
    • Stephen P.A. Fodor,
    • Danilo A. Tagle,
    • and Francis S. Collins
    Genome Res. December 1, 1998 8: 1245-1258; doi:10.1101/gr.8.12.1245
    ...for complete analysis of the entire ATM genomic coding and splice junction sequences in a single reaction, and most require gel electrophoresis, which complicates scale-up and automation. The RT–PCR methods carry a further risk of missing mutations that result in unstable RNA. Significant evidence exists...
  10. ARTICLE: Metastable single-strand DNA conformational polymorphism analysis results in enhanced polymorphism detection.
    • T Kasuga,
    • J Cheng,
    • and K R Mitchelson
    Genome Res. February 1995 4: 227-233
    ..., H., Yoshimoto, K. Mizusawa, N. Kudo, E. and Itakura. M. 1994 . Multiple fluorescence-based PCR-SSCP analysis. BioTechniques 16 : 296 – 305 . 19.. Sarkar, G., , Yoon, H-S. , Sommer. S.S. Sarkar, G., Yoon, H-S. and Sommer. S.S. 1992 . Screening for mutations by RNA single-strand conformation...
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