An intermediate grade of finished genomic sequence suitable for comparative analyses

Robert W. Blakesley(National Institutes of Health), Nancy F. Hansen(Office of Extramural Research), James C. Mullikin(National Institutes of Health), Pamela J. Thomas(Office of Extramural Research), Jennifer C. McDowell(Office of Extramural Research), Baishali Maskeri(Office of Extramural Research), Alice Young(Office of Extramural Research), Beatrice Benjamin(Office of Extramural Research), Shelise Brooks(Office of Extramural Research), Bradley I. Coleman(Office of Extramural Research), Jyoti Gupta(Office of Extramural Research), Shi-ling Ho, Eric Karlins(Office of Extramural Research), Quino Maduro(Office of Extramural Research), Sirintorn Stantripop(Office of Extramural Research), Cyrus Tsurgeon(Office of Extramural Research), Jennifer Vogt(Office of Extramural Research), Michelle Walker(Office of Extramural Research), Catherine A. Masiello(Office of Extramural Research), Xiaobin Guan(Office of Extramural Research), NISC Comparative Sequencing Program(National Institutes of Health), Gerard G. Bouffard(National Institutes of Health), Eric D. Green(National Institutes of Health)
Genome Research
October 12, 2004
Cited by 75Open Access
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Abstract

Although the cost of generating draft-quality genomic sequence continues to decline, refining that sequence by the process of "sequence finishing" remains expensive. Near-perfect finished sequence is an appropriate goal for the human genome and a small set of reference genomes; however, such a high-quality product cannot be cost-justified for large numbers of additional genomes, at least for the foreseeable future. Here we describe the generation and quality of an intermediate grade of finished genomic sequence (termed comparative-grade finished sequence), which is tailored for use in multispecies sequence comparisons. Our analyses indicate that this sequence is very high quality (with the residual gaps and errors mostly falling within repetitive elements) and reflects 99% of the total sequence. Importantly, comparative-grade sequence finishing requires approximately 40-fold less reagents and approximately 10-fold less personnel effort compared to the generation of near-perfect finished sequence, such as that produced for the human genome. Although applied here to finishing sequence derived from individual bacterial artificial chromosome (BAC) clones, one could envision establishing routines for refining sequences emanating from whole-genome shotgun sequencing projects to a similar quality level. Our experience to date demonstrates that comparative-grade sequence finishing represents a practical and affordable option for sequence refinement en route to comparative analyses.


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