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 |
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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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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.</description><identifier>ISSN: 1088-9051</identifier><identifier>EISSN: 1549-5469</identifier><identifier>DOI: 10.1101/gr.2648404</identifier><identifier>PMID: 15479945</identifier><language>eng</language><publisher>United States: Cold Spring Harbor Laboratory Press</publisher><subject>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</subject><ispartof>Genome research, 2004-11, Vol.14 (11), p.2235-2244</ispartof><rights>Copyright © 2004, Cold Spring Harbor Laboratory Press 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-45a30acd239c792b98a6f6d0f72606f91c4bf42bda533e7880121b3000f9a8fb3</citedby><cites>FETCH-LOGICAL-c404t-45a30acd239c792b98a6f6d0f72606f91c4bf42bda533e7880121b3000f9a8fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC525681/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC525681/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15479945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blakesley, Robert W</creatorcontrib><creatorcontrib>Hansen, Nancy F</creatorcontrib><creatorcontrib>Mullikin, James C</creatorcontrib><creatorcontrib>Thomas, Pamela J</creatorcontrib><creatorcontrib>McDowell, Jennifer C</creatorcontrib><creatorcontrib>Maskeri, Baishali</creatorcontrib><creatorcontrib>Young, Alice C</creatorcontrib><creatorcontrib>Benjamin, Beatrice</creatorcontrib><creatorcontrib>Brooks, Shelise Y</creatorcontrib><creatorcontrib>Coleman, Bradley I</creatorcontrib><creatorcontrib>Gupta, Jyoti</creatorcontrib><creatorcontrib>Ho, Shi-Ling</creatorcontrib><creatorcontrib>Karlins, Eric M</creatorcontrib><creatorcontrib>Maduro, Quino L</creatorcontrib><creatorcontrib>Stantripop, Sirintorn</creatorcontrib><creatorcontrib>Tsurgeon, Cyrus</creatorcontrib><creatorcontrib>Vogt, Jennifer L</creatorcontrib><creatorcontrib>Walker, Michelle A</creatorcontrib><creatorcontrib>Masiello, Catherine A</creatorcontrib><creatorcontrib>Guan, Xiaobin</creatorcontrib><creatorcontrib>Bouffard, Gerard G</creatorcontrib><creatorcontrib>Green, Eric D</creatorcontrib><creatorcontrib>NISC Comparative Sequencing Program</creatorcontrib><title>An intermediate grade of finished genomic sequence suitable for comparative analyses</title><title>Genome research</title><addtitle>Genome Res</addtitle><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.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Chromosomes, Artificial, Bacterial - genetics</subject><subject>Cloning, Molecular</subject><subject>Computational Biology</subject><subject>Contig Mapping - economics</subject><subject>Contig Mapping - methods</subject><subject>Costs and Cost Analysis</subject><subject>Databases, Genetic</subject><subject>Exons - genetics</subject><subject>Genome</subject><subject>Lemur - genetics</subject><subject>Letters</subject><subject>Molecular Sequence Data</subject><subject>Papio - genetics</subject><subject>Rats</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>Sequence Analysis, DNA - economics</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Software - economics</subject><issn>1088-9051</issn><issn>1549-5469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtr3TAQhUVpaR7tJj-gaNVFwalkS5a06CKE5gGBbJK1GMsjR8WWbiTfQP59FHJJ0lVWMzDfGc7hEHLE2THnjP-e8nHbCy2Y-ET2uRSmkaI3n-vOtG4Mk3yPHJTyjzHWCa2_kr0KKWOE3Cc3J5GGuGJecAywIp0yjEiTpz7EUO5wpBPGtARHC95vMTqkZRtWGGakPmXq0rKBDGt4QAoR5seC5Rv54mEu-H03D8nt2d-b04vm6vr88vTkqnHV69oICR0DN7adccq0g9HQ-35kXrU9673hTgxetMMIsutQac14y4euxvAGtB-6Q_Ln5e9mO1T_DuOaYbabHBbIjzZBsP9fYrizU3qwspW95lX_c6fPqWYrq11CcTjPEDFti-0Va5US-kOQK8WM0LKCv15Al1MpGf2rGc7sc1l2ynZXVoV_vLf_hu7a6Z4AOdmRUA</recordid><startdate>200411</startdate><enddate>200411</enddate><creator>Blakesley, Robert W</creator><creator>Hansen, Nancy F</creator><creator>Mullikin, James C</creator><creator>Thomas, Pamela J</creator><creator>McDowell, Jennifer C</creator><creator>Maskeri, Baishali</creator><creator>Young, Alice C</creator><creator>Benjamin, Beatrice</creator><creator>Brooks, Shelise Y</creator><creator>Coleman, Bradley I</creator><creator>Gupta, Jyoti</creator><creator>Ho, Shi-Ling</creator><creator>Karlins, Eric M</creator><creator>Maduro, Quino L</creator><creator>Stantripop, Sirintorn</creator><creator>Tsurgeon, Cyrus</creator><creator>Vogt, Jennifer L</creator><creator>Walker, Michelle A</creator><creator>Masiello, Catherine A</creator><creator>Guan, Xiaobin</creator><creator>Bouffard, Gerard G</creator><creator>Green, Eric D</creator><general>Cold Spring Harbor Laboratory Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200411</creationdate><title>An intermediate grade of finished genomic sequence suitable for comparative analyses</title><author>Blakesley, Robert W ; 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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.</abstract><cop>United States</cop><pub>Cold Spring Harbor Laboratory Press</pub><pmid>15479945</pmid><doi>10.1101/gr.2648404</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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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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