An intermediate grade of finished genomic sequence suitable for comparative analyses

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, su...

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Veröffentlicht in:Genome research 2004-11, Vol.14 (11), p.2235-2244
Hauptverfasser: Blakesley, Robert W, Hansen, Nancy F, Mullikin, James C, Thomas, Pamela J, McDowell, Jennifer C, Maskeri, Baishali, Young, Alice C, Benjamin, Beatrice, Brooks, Shelise Y, Coleman, Bradley I, Gupta, Jyoti, Ho, Shi-Ling, Karlins, Eric M, Maduro, Quino L, Stantripop, Sirintorn, Tsurgeon, Cyrus, Vogt, Jennifer L, Walker, Michelle A, Masiello, Catherine A, Guan, Xiaobin, Bouffard, Gerard G, Green, Eric D
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container_end_page 2244
container_issue 11
container_start_page 2235
container_title Genome research
container_volume 14
creator Blakesley, Robert W
Hansen, Nancy F
Mullikin, James C
Thomas, Pamela J
McDowell, Jennifer C
Maskeri, Baishali
Young, Alice C
Benjamin, Beatrice
Brooks, Shelise Y
Coleman, Bradley I
Gupta, Jyoti
Ho, Shi-Ling
Karlins, Eric M
Maduro, Quino L
Stantripop, Sirintorn
Tsurgeon, Cyrus
Vogt, Jennifer L
Walker, Michelle A
Masiello, Catherine A
Guan, Xiaobin
Bouffard, Gerard G
Green, Eric D
description 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.
doi_str_mv 10.1101/gr.2648404
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subjects Animals
Base Sequence
Chromosomes, Artificial, Bacterial - genetics
Cloning, Molecular
Computational Biology
Contig Mapping - economics
Contig Mapping - methods
Costs and Cost Analysis
Databases, Genetic
Exons - genetics
Genome
Lemur - genetics
Letters
Molecular Sequence Data
Papio - genetics
Rats
Repetitive Sequences, Nucleic Acid
Sequence Analysis, DNA - economics
Sequence Homology, Nucleic Acid
Software - economics
title An intermediate grade of finished genomic sequence suitable for comparative analyses
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