We use cookies to improve your experience. By continuing to browse this site, you accept our cookie policy.×
Short Technical ReportsOpen Accesscc iconby icon

PCR Template Preparation for Capillary DNA Sequencing

    W.A. Silva

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    M.C.R. Costa

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    V. Valente

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    J. de Freitas Sousa

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    M.L. Paçó-Larson

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    E.M. Espreafico

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    S.S. Camargo

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    E. Monteiro

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    A. de Jesus Holanda

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    M.A. Zago

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    ,
    A.J.G. Simpson

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    &
    E.D. Neto

    *Address correspondence to Dr. Emmanuel Dias Neto, Ludwig Institute for Cancer Research, R. Prof. Antônio Prudente, 109-4th floor, 01509-010, São Paulo, SP Brazil. e-mail:

    E-mail Address: emmanuel@ludwig.org.br

    Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil

    Published Online:https://doi.org/10.2144/01303st05

    Fluorescence-based capillary DNA sequencing has facilitated the early completion of several complex sequencing projects. While capillary systems offer great benefits in terms of ease of use and automation, we find that they are sufficiently different from slab gel separation methodologies, demanding re-examination of the protocols used to generate and use DNA sequencing templates. We have recently initiated a largescale Human Open Reading Frame™ EST project involving 30 laboratories feeding 11 MegaBace™ 1000 capillary sequencers. The group has already produced more than 300000 valid sequences. The most successful template preparation protocol we have found is described here. We have found that a crucial step is the standardization of the quantity and quality of the templates, which have been achieved by overnight bacterial culture followed by PCR using limiting amounts of primers. Using this protocol, there is no need for post-PCR purification, and the final preparation cost is US $0.09/template. After sequencing 10848 templates using this protocol, 78% of the reads were accepted (after discarding vectors without inserts and inserts smaller than 100 nucleotides), and 85% of the total number of bases had Phred scores of 15 or above.