Piercing the dark matter: bioinformatics of long-range sequencing and mapping

Several new genomics technologies have become available that offer long-read sequencing or long-range mapping with higher throughput and higher resolution analysis than ever before. These long-range technologies are rapidly advancing the field with improved reference genomes, more comprehensive vari...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature reviews. Genetics 2018-06, Vol.19 (6), p.329-346
Hauptverfasser: Sedlazeck, Fritz J., Lee, Hayan, Darby, Charlotte A., Schatz, Michael C.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 346
container_issue 6
container_start_page 329
container_title Nature reviews. Genetics
container_volume 19
creator Sedlazeck, Fritz J.
Lee, Hayan
Darby, Charlotte A.
Schatz, Michael C.
description Several new genomics technologies have become available that offer long-read sequencing or long-range mapping with higher throughput and higher resolution analysis than ever before. These long-range technologies are rapidly advancing the field with improved reference genomes, more comprehensive variant identification and more complete views of transcriptomes and epigenomes. However, they also require new bioinformatics approaches to take full advantage of their unique characteristics while overcoming their complex errors and modalities. Here, we discuss several of the most important applications of the new technologies, focusing on both the currently available bioinformatics tools and opportunities for future research. Various genomics-related fields are increasingly taking advantage of long-read sequencing and long-range mapping technologies, but making sense of the data requires new analysis strategies. This Review discusses bioinformatics tools that have been devised to handle the numerous characteristic features of these long-range data types, with applications in genome assembly, genetic variant detection, haplotype phasing, transcriptomics and epigenomics.
doi_str_mv 10.1038/s41576-018-0003-4
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2020493842</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A572620315</galeid><sourcerecordid>A572620315</sourcerecordid><originalsourceid>FETCH-LOGICAL-c570t-1053a75e3504c28c0632dbfe1ce8176266d52f4aaf7946f9068ac201fc8290f43</originalsourceid><addsrcrecordid>eNp1kk1v1DAQhiMEoqXwA7igSEioPaSMHdtJuFVVoZWKQHycLa8zzrok9tZ2JPj3ON3SdhHIB8_Yzzsaj9-ieEngmEDdvo2M8EZUQNoKAOqKPSr2CWtIzgR7fBdzsVc8i_EKgAjS1E-LPdrxruNA9ouPny0Gbd1QpjWWvQo_ykmlhOFdubLeOuNDzq2OpTfl6N1QBeUGLCNez-huhMr1WbPZ5Ph58cSoMeKL2_2g-P7-7NvpeXX56cPF6cllpXkDqSLAa9VwrDkwTVsNoqb9yiDR2JJGUCF6Tg1TyjQdE6YD0SpNgRjd0g4Mqw-Kw23dTfC5j5jkZKPGcVQO_RwlBQqsq1tGM_r6L_TKz8Hl7jJVd5S3hPF7alAjyuXZKSi9FJUnvKEio2Shjv9B5dXjZLV3aGw-3xEc7Qgyk_BnGtQco7z4-mWXffOAXaMa0zr6cU7Wu7gLki2og48xoJGbYCcVfkkCcvGF3PpCZl_IxRdyGdir2ynMqwn7O8UfI2SAboGYr_IHh_sx_b_qb9rsvXY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2039258145</pqid></control><display><type>article</type><title>Piercing the dark matter: bioinformatics of long-range sequencing and mapping</title><source>Springer Nature - Complete Springer Journals</source><source>Nature</source><creator>Sedlazeck, Fritz J. ; Lee, Hayan ; Darby, Charlotte A. ; Schatz, Michael C.</creator><creatorcontrib>Sedlazeck, Fritz J. ; Lee, Hayan ; Darby, Charlotte A. ; Schatz, Michael C.</creatorcontrib><description>Several new genomics technologies have become available that offer long-read sequencing or long-range mapping with higher throughput and higher resolution analysis than ever before. These long-range technologies are rapidly advancing the field with improved reference genomes, more comprehensive variant identification and more complete views of transcriptomes and epigenomes. However, they also require new bioinformatics approaches to take full advantage of their unique characteristics while overcoming their complex errors and modalities. Here, we discuss several of the most important applications of the new technologies, focusing on both the currently available bioinformatics tools and opportunities for future research. Various genomics-related fields are increasingly taking advantage of long-read sequencing and long-range mapping technologies, but making sense of the data requires new analysis strategies. This Review discusses bioinformatics tools that have been devised to handle the numerous characteristic features of these long-range data types, with applications in genome assembly, genetic variant detection, haplotype phasing, transcriptomics and epigenomics.</description><identifier>ISSN: 1471-0056</identifier><identifier>EISSN: 1471-0064</identifier><identifier>DOI: 10.1038/s41576-018-0003-4</identifier><identifier>PMID: 29599501</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/39 ; 631/1647/48 ; 631/208/212/2302 ; 631/208/514/2254 ; 631/208/726 ; Agriculture ; Animal Genetics and Genomics ; Bioinformatics ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Chromosome mapping ; Computational biology ; DNA sequencing ; Gene Function ; Gene mapping ; Genetic research ; Genomes ; Genomics ; Human Genetics ; Review Article ; Technology</subject><ispartof>Nature reviews. Genetics, 2018-06, Vol.19 (6), p.329-346</ispartof><rights>Macmillan Publishers Ltd., part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jun 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-1053a75e3504c28c0632dbfe1ce8176266d52f4aaf7946f9068ac201fc8290f43</citedby><cites>FETCH-LOGICAL-c570t-1053a75e3504c28c0632dbfe1ce8176266d52f4aaf7946f9068ac201fc8290f43</cites><orcidid>0000-0003-0571-3192 ; 0000-0003-2195-5300 ; 0000-0001-6040-2691</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41576-018-0003-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41576-018-0003-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29599501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sedlazeck, Fritz J.</creatorcontrib><creatorcontrib>Lee, Hayan</creatorcontrib><creatorcontrib>Darby, Charlotte A.</creatorcontrib><creatorcontrib>Schatz, Michael C.</creatorcontrib><title>Piercing the dark matter: bioinformatics of long-range sequencing and mapping</title><title>Nature reviews. Genetics</title><addtitle>Nat Rev Genet</addtitle><addtitle>Nat Rev Genet</addtitle><description>Several new genomics technologies have become available that offer long-read sequencing or long-range mapping with higher throughput and higher resolution analysis than ever before. These long-range technologies are rapidly advancing the field with improved reference genomes, more comprehensive variant identification and more complete views of transcriptomes and epigenomes. However, they also require new bioinformatics approaches to take full advantage of their unique characteristics while overcoming their complex errors and modalities. Here, we discuss several of the most important applications of the new technologies, focusing on both the currently available bioinformatics tools and opportunities for future research. Various genomics-related fields are increasingly taking advantage of long-read sequencing and long-range mapping technologies, but making sense of the data requires new analysis strategies. This Review discusses bioinformatics tools that have been devised to handle the numerous characteristic features of these long-range data types, with applications in genome assembly, genetic variant detection, haplotype phasing, transcriptomics and epigenomics.</description><subject>38/39</subject><subject>631/1647/48</subject><subject>631/208/212/2302</subject><subject>631/208/514/2254</subject><subject>631/208/726</subject><subject>Agriculture</subject><subject>Animal Genetics and Genomics</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Chromosome mapping</subject><subject>Computational biology</subject><subject>DNA sequencing</subject><subject>Gene Function</subject><subject>Gene mapping</subject><subject>Genetic research</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Human Genetics</subject><subject>Review Article</subject><subject>Technology</subject><issn>1471-0056</issn><issn>1471-0064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp1kk1v1DAQhiMEoqXwA7igSEioPaSMHdtJuFVVoZWKQHycLa8zzrok9tZ2JPj3ON3SdhHIB8_Yzzsaj9-ieEngmEDdvo2M8EZUQNoKAOqKPSr2CWtIzgR7fBdzsVc8i_EKgAjS1E-LPdrxruNA9ouPny0Gbd1QpjWWvQo_ykmlhOFdubLeOuNDzq2OpTfl6N1QBeUGLCNez-huhMr1WbPZ5Ph58cSoMeKL2_2g-P7-7NvpeXX56cPF6cllpXkDqSLAa9VwrDkwTVsNoqb9yiDR2JJGUCF6Tg1TyjQdE6YD0SpNgRjd0g4Mqw-Kw23dTfC5j5jkZKPGcVQO_RwlBQqsq1tGM_r6L_TKz8Hl7jJVd5S3hPF7alAjyuXZKSi9FJUnvKEio2Shjv9B5dXjZLV3aGw-3xEc7Qgyk_BnGtQco7z4-mWXffOAXaMa0zr6cU7Wu7gLki2og48xoJGbYCcVfkkCcvGF3PpCZl_IxRdyGdir2ynMqwn7O8UfI2SAboGYr_IHh_sx_b_qb9rsvXY</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Sedlazeck, Fritz J.</creator><creator>Lee, Hayan</creator><creator>Darby, Charlotte A.</creator><creator>Schatz, Michael C.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0571-3192</orcidid><orcidid>https://orcid.org/0000-0003-2195-5300</orcidid><orcidid>https://orcid.org/0000-0001-6040-2691</orcidid></search><sort><creationdate>20180601</creationdate><title>Piercing the dark matter: bioinformatics of long-range sequencing and mapping</title><author>Sedlazeck, Fritz J. ; Lee, Hayan ; Darby, Charlotte A. ; Schatz, Michael C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-1053a75e3504c28c0632dbfe1ce8176266d52f4aaf7946f9068ac201fc8290f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>38/39</topic><topic>631/1647/48</topic><topic>631/208/212/2302</topic><topic>631/208/514/2254</topic><topic>631/208/726</topic><topic>Agriculture</topic><topic>Animal Genetics and Genomics</topic><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Chromosome mapping</topic><topic>Computational biology</topic><topic>DNA sequencing</topic><topic>Gene Function</topic><topic>Gene mapping</topic><topic>Genetic research</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Human Genetics</topic><topic>Review Article</topic><topic>Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sedlazeck, Fritz J.</creatorcontrib><creatorcontrib>Lee, Hayan</creatorcontrib><creatorcontrib>Darby, Charlotte A.</creatorcontrib><creatorcontrib>Schatz, Michael C.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Proquest Nursing &amp; Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sedlazeck, Fritz J.</au><au>Lee, Hayan</au><au>Darby, Charlotte A.</au><au>Schatz, Michael C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Piercing the dark matter: bioinformatics of long-range sequencing and mapping</atitle><jtitle>Nature reviews. Genetics</jtitle><stitle>Nat Rev Genet</stitle><addtitle>Nat Rev Genet</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>19</volume><issue>6</issue><spage>329</spage><epage>346</epage><pages>329-346</pages><issn>1471-0056</issn><eissn>1471-0064</eissn><abstract>Several new genomics technologies have become available that offer long-read sequencing or long-range mapping with higher throughput and higher resolution analysis than ever before. These long-range technologies are rapidly advancing the field with improved reference genomes, more comprehensive variant identification and more complete views of transcriptomes and epigenomes. However, they also require new bioinformatics approaches to take full advantage of their unique characteristics while overcoming their complex errors and modalities. Here, we discuss several of the most important applications of the new technologies, focusing on both the currently available bioinformatics tools and opportunities for future research. Various genomics-related fields are increasingly taking advantage of long-read sequencing and long-range mapping technologies, but making sense of the data requires new analysis strategies. This Review discusses bioinformatics tools that have been devised to handle the numerous characteristic features of these long-range data types, with applications in genome assembly, genetic variant detection, haplotype phasing, transcriptomics and epigenomics.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29599501</pmid><doi>10.1038/s41576-018-0003-4</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-0571-3192</orcidid><orcidid>https://orcid.org/0000-0003-2195-5300</orcidid><orcidid>https://orcid.org/0000-0001-6040-2691</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1471-0056
ispartof Nature reviews. Genetics, 2018-06, Vol.19 (6), p.329-346
issn 1471-0056
1471-0064
language eng
recordid cdi_proquest_miscellaneous_2020493842
source Springer Nature - Complete Springer Journals; Nature
subjects 38/39
631/1647/48
631/208/212/2302
631/208/514/2254
631/208/726
Agriculture
Animal Genetics and Genomics
Bioinformatics
Biomedical and Life Sciences
Biomedicine
Cancer Research
Chromosome mapping
Computational biology
DNA sequencing
Gene Function
Gene mapping
Genetic research
Genomes
Genomics
Human Genetics
Review Article
Technology
title Piercing the dark matter: bioinformatics of long-range sequencing and mapping
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T03%3A01%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Piercing%20the%20dark%20matter:%20bioinformatics%20of%20long-range%20sequencing%20and%20mapping&rft.jtitle=Nature%20reviews.%20Genetics&rft.au=Sedlazeck,%20Fritz%20J.&rft.date=2018-06-01&rft.volume=19&rft.issue=6&rft.spage=329&rft.epage=346&rft.pages=329-346&rft.issn=1471-0056&rft.eissn=1471-0064&rft_id=info:doi/10.1038/s41576-018-0003-4&rft_dat=%3Cgale_proqu%3EA572620315%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2039258145&rft_id=info:pmid/29599501&rft_galeid=A572620315&rfr_iscdi=true