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PCR Template Preparation for Capillary DNA Sequencing
Author(s) -
Wilson A. Silva,
María Costa,
Valéria Valente,
Josane F. Sousa,
Maria Luisa PaçóLarson,
Enilza Maria Espreáfico,
Solange Soares de Camargo,
Emily Rodrigues Monteiro,
Adriano de Jesus Holanda,
Marco A. Zago,
Andrew J.G. Simpson,
Emmanuel DiasNeto
Publication year - 2001
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/01303st05
Subject(s) - template , capillary electrophoresis , protocol (science) , dna sequencing , dna sequencer , computational biology , biology , standardization , polymerase chain reaction , limiting , dna , capillary action , chromatography , computer science , microbiology and biotechnology , genetics , chemistry , gene , programming language , materials science , medicine , alternative medicine , pathology , operating system , mechanical engineering , engineering , composite material
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 large-scale Human Open Reading Frame EST project involving 30 laboratories feeding 11 MegaBace 1000 capillary sequencers. The group has already produced more than 300,000 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 10,848 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.

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