Building the sequence map of the human pan-genome
Here we integrate the de novo assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified ∼5 Mb of novel sequences not present in the reference genome in each of these assemblies. Most novel sequences are individu...
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Veröffentlicht in: | Nature biotechnology 2010, Vol.28 (1), p.57-63 |
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creator | Li, Ruiqiang Li, Yingrui Zheng, Hancheng Luo, Ruibang Zhu, Hongmei Li, Qibin Qian, Wubin Ren, Yuanyuan Tian, Geng Li, Jinxiang Zhou, Guangyu Zhu, Xuan Wu, Honglong Qin, Junjie Jin, Xin Li, Dongfang Cao, Hongzhi Hu, Xueda Blanche, Hélène Cann, Howard Zhang, Xiuqing Li, Songgang Bolund, Lars Kristiansen, Karsten Yang, Huanming Wang, Jun Wang, Jian |
description | Here we integrate the
de novo
assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified ∼5 Mb of novel sequences not present in the reference genome in each of these assemblies. Most novel sequences are individual or population specific, as revealed by their comparison to all available human DNA sequence and by PCR validation using the human genome diversity cell line panel. We found novel sequences present in patterns consistent with known human migration paths. Cross-species conservation analysis of predicted genes indicated that the novel sequences contain potentially functional coding regions. We estimate that a complete human pan-genome would contain ∼19–40 Mb of novel sequence not present in the extant reference genome. The extensive amount of novel sequence contributing to the genetic variation of the pan-genome indicates the importance of using complete genome sequencing and
de novo
assembly. |
doi_str_mv | 10.1038/nbt.1596 |
format | Article |
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de novo
assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified ∼5 Mb of novel sequences not present in the reference genome in each of these assemblies. Most novel sequences are individual or population specific, as revealed by their comparison to all available human DNA sequence and by PCR validation using the human genome diversity cell line panel. We found novel sequences present in patterns consistent with known human migration paths. Cross-species conservation analysis of predicted genes indicated that the novel sequences contain potentially functional coding regions. We estimate that a complete human pan-genome would contain ∼19–40 Mb of novel sequence not present in the extant reference genome. The extensive amount of novel sequence contributing to the genetic variation of the pan-genome indicates the importance of using complete genome sequencing and
de novo
assembly.</description><identifier>ISSN: 1087-0156</identifier><identifier>EISSN: 1546-1696</identifier><identifier>DOI: 10.1038/nbt.1596</identifier><identifier>PMID: 19997067</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Agriculture ; analysis ; Animals ; Base Sequence ; Bioinformatics ; Biomedical Engineering/Biotechnology ; Biomedicine ; Biotechnology ; Deoxyribonucleic acid ; Disease susceptibility ; DNA ; Genetic aspects ; Genetic diversity ; Genetic variation ; Genetics, Population ; Genome, Human - genetics ; Genomics ; Human genome ; Humans ; Life Sciences ; Migratory species ; Population genetics ; Sequence Alignment ; Sequence Analysis, DNA - methods ; Species Specificity</subject><ispartof>Nature biotechnology, 2010, Vol.28 (1), p.57-63</ispartof><rights>Springer Nature Limited 2010</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jan 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c612t-5e16081d97c703e268cd32ec403839e75662c721094f328f7bcee41830566e1d3</citedby><cites>FETCH-LOGICAL-c612t-5e16081d97c703e268cd32ec403839e75662c721094f328f7bcee41830566e1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nbt.1596$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nbt.1596$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19997067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ruiqiang</creatorcontrib><creatorcontrib>Li, Yingrui</creatorcontrib><creatorcontrib>Zheng, Hancheng</creatorcontrib><creatorcontrib>Luo, Ruibang</creatorcontrib><creatorcontrib>Zhu, Hongmei</creatorcontrib><creatorcontrib>Li, Qibin</creatorcontrib><creatorcontrib>Qian, Wubin</creatorcontrib><creatorcontrib>Ren, Yuanyuan</creatorcontrib><creatorcontrib>Tian, Geng</creatorcontrib><creatorcontrib>Li, Jinxiang</creatorcontrib><creatorcontrib>Zhou, Guangyu</creatorcontrib><creatorcontrib>Zhu, Xuan</creatorcontrib><creatorcontrib>Wu, Honglong</creatorcontrib><creatorcontrib>Qin, Junjie</creatorcontrib><creatorcontrib>Jin, Xin</creatorcontrib><creatorcontrib>Li, Dongfang</creatorcontrib><creatorcontrib>Cao, Hongzhi</creatorcontrib><creatorcontrib>Hu, Xueda</creatorcontrib><creatorcontrib>Blanche, Hélène</creatorcontrib><creatorcontrib>Cann, Howard</creatorcontrib><creatorcontrib>Zhang, Xiuqing</creatorcontrib><creatorcontrib>Li, Songgang</creatorcontrib><creatorcontrib>Bolund, Lars</creatorcontrib><creatorcontrib>Kristiansen, Karsten</creatorcontrib><creatorcontrib>Yang, Huanming</creatorcontrib><creatorcontrib>Wang, Jun</creatorcontrib><creatorcontrib>Wang, Jian</creatorcontrib><title>Building the sequence map of the human pan-genome</title><title>Nature biotechnology</title><addtitle>Nat Biotechnol</addtitle><addtitle>Nat Biotechnol</addtitle><description>Here we integrate the
de novo
assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified ∼5 Mb of novel sequences not present in the reference genome in each of these assemblies. Most novel sequences are individual or population specific, as revealed by their comparison to all available human DNA sequence and by PCR validation using the human genome diversity cell line panel. We found novel sequences present in patterns consistent with known human migration paths. Cross-species conservation analysis of predicted genes indicated that the novel sequences contain potentially functional coding regions. We estimate that a complete human pan-genome would contain ∼19–40 Mb of novel sequence not present in the extant reference genome. The extensive amount of novel sequence contributing to the genetic variation of the pan-genome indicates the importance of using complete genome sequencing and
de novo
assembly.</description><subject>Agriculture</subject><subject>analysis</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Bioinformatics</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Deoxyribonucleic acid</subject><subject>Disease susceptibility</subject><subject>DNA</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic variation</subject><subject>Genetics, Population</subject><subject>Genome, Human - genetics</subject><subject>Genomics</subject><subject>Human genome</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Migratory species</subject><subject>Population genetics</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA - methods</subject><subject>Species 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de novo
assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified ∼5 Mb of novel sequences not present in the reference genome in each of these assemblies. Most novel sequences are individual or population specific, as revealed by their comparison to all available human DNA sequence and by PCR validation using the human genome diversity cell line panel. We found novel sequences present in patterns consistent with known human migration paths. Cross-species conservation analysis of predicted genes indicated that the novel sequences contain potentially functional coding regions. We estimate that a complete human pan-genome would contain ∼19–40 Mb of novel sequence not present in the extant reference genome. The extensive amount of novel sequence contributing to the genetic variation of the pan-genome indicates the importance of using complete genome sequencing and
de novo
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source | MEDLINE; Springer Nature - Complete Springer Journals; Nature |
subjects | Agriculture analysis Animals Base Sequence Bioinformatics Biomedical Engineering/Biotechnology Biomedicine Biotechnology Deoxyribonucleic acid Disease susceptibility DNA Genetic aspects Genetic diversity Genetic variation Genetics, Population Genome, Human - genetics Genomics Human genome Humans Life Sciences Migratory species Population genetics Sequence Alignment Sequence Analysis, DNA - methods Species Specificity |
title | Building the sequence map of the human pan-genome |
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