CRISPRidentify: identification of CRISPR arrays using machine learning approach
Abstract CRISPR–Cas are adaptive immune systems that degrade foreign genetic elements in archaea and bacteria. In carrying out their immune functions, CRISPR–Cas systems heavily rely on RNA components. These CRISPR (cr) RNAs are repeat-spacer units that are produced by processing of pre-crRNA, the t...
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creator | Mitrofanov, Alexander Alkhnbashi, Omer S Shmakov, Sergey A Makarova, Kira S Koonin, Eugene V Backofen, Rolf |
description | Abstract
CRISPR–Cas are adaptive immune systems that degrade foreign genetic elements in archaea and bacteria. In carrying out their immune functions, CRISPR–Cas systems heavily rely on RNA components. These CRISPR (cr) RNAs are repeat-spacer units that are produced by processing of pre-crRNA, the transcript of CRISPR arrays, and guide Cas protein(s) to the cognate invading nucleic acids, enabling their destruction. Several bioinformatics tools have been developed to detect CRISPR arrays based solely on DNA sequences, but all these tools employ the same strategy of looking for repetitive patterns, which might correspond to CRISPR array repeats. The identified patterns are evaluated using a fixed, built-in scoring function, and arrays exceeding a cut-off value are reported. Here, we instead introduce a data-driven approach that uses machine learning to detect and differentiate true CRISPR arrays from false ones based on several features. Our CRISPR detection tool, CRISPRidentify, performs three steps: detection, feature extraction and classification based on manually curated sets of positive and negative examples of CRISPR arrays. The identified CRISPR arrays are then reported to the user accompanied by detailed annotation. We demonstrate that our approach identifies not only previously detected CRISPR arrays, but also CRISPR array candidates not detected by other tools. Compared to other methods, our tool has a drastically reduced false positive rate. In contrast to the existing tools, our approach not only provides the user with the basic statistics on the identified CRISPR arrays but also produces a certainty score as a practical measure of the likelihood that a given genomic region is a CRISPR array. |
doi_str_mv | 10.1093/nar/gkaa1158 |
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CRISPR–Cas are adaptive immune systems that degrade foreign genetic elements in archaea and bacteria. In carrying out their immune functions, CRISPR–Cas systems heavily rely on RNA components. These CRISPR (cr) RNAs are repeat-spacer units that are produced by processing of pre-crRNA, the transcript of CRISPR arrays, and guide Cas protein(s) to the cognate invading nucleic acids, enabling their destruction. Several bioinformatics tools have been developed to detect CRISPR arrays based solely on DNA sequences, but all these tools employ the same strategy of looking for repetitive patterns, which might correspond to CRISPR array repeats. The identified patterns are evaluated using a fixed, built-in scoring function, and arrays exceeding a cut-off value are reported. Here, we instead introduce a data-driven approach that uses machine learning to detect and differentiate true CRISPR arrays from false ones based on several features. Our CRISPR detection tool, CRISPRidentify, performs three steps: detection, feature extraction and classification based on manually curated sets of positive and negative examples of CRISPR arrays. The identified CRISPR arrays are then reported to the user accompanied by detailed annotation. We demonstrate that our approach identifies not only previously detected CRISPR arrays, but also CRISPR array candidates not detected by other tools. Compared to other methods, our tool has a drastically reduced false positive rate. In contrast to the existing tools, our approach not only provides the user with the basic statistics on the identified CRISPR arrays but also produces a certainty score as a practical measure of the likelihood that a given genomic region is a CRISPR array.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkaa1158</identifier><identifier>PMID: 33290505</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Clustered Regularly Interspaced Short Palindromic Repeats ; Genome, Archaeal ; Genome, Bacterial ; Machine Learning ; Methods Online ; Software</subject><ispartof>Nucleic acids research, 2021-02, Vol.49 (4), p.e20-e20</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. 2021</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-5ccea99ce6ac031cd0c820448f1b466de437596629cd79dc53073a41001625b93</citedby><cites>FETCH-LOGICAL-c416t-5ccea99ce6ac031cd0c820448f1b466de437596629cd79dc53073a41001625b93</cites><orcidid>0000-0001-8088-590X ; 0000-0003-3943-8299 ; 0000-0001-8231-3323 ; 0000-0002-8174-2844</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913763/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913763/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1604,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33290505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitrofanov, Alexander</creatorcontrib><creatorcontrib>Alkhnbashi, Omer S</creatorcontrib><creatorcontrib>Shmakov, Sergey A</creatorcontrib><creatorcontrib>Makarova, Kira S</creatorcontrib><creatorcontrib>Koonin, Eugene V</creatorcontrib><creatorcontrib>Backofen, Rolf</creatorcontrib><title>CRISPRidentify: identification of CRISPR arrays using machine learning approach</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
CRISPR–Cas are adaptive immune systems that degrade foreign genetic elements in archaea and bacteria. In carrying out their immune functions, CRISPR–Cas systems heavily rely on RNA components. These CRISPR (cr) RNAs are repeat-spacer units that are produced by processing of pre-crRNA, the transcript of CRISPR arrays, and guide Cas protein(s) to the cognate invading nucleic acids, enabling their destruction. Several bioinformatics tools have been developed to detect CRISPR arrays based solely on DNA sequences, but all these tools employ the same strategy of looking for repetitive patterns, which might correspond to CRISPR array repeats. The identified patterns are evaluated using a fixed, built-in scoring function, and arrays exceeding a cut-off value are reported. Here, we instead introduce a data-driven approach that uses machine learning to detect and differentiate true CRISPR arrays from false ones based on several features. Our CRISPR detection tool, CRISPRidentify, performs three steps: detection, feature extraction and classification based on manually curated sets of positive and negative examples of CRISPR arrays. The identified CRISPR arrays are then reported to the user accompanied by detailed annotation. We demonstrate that our approach identifies not only previously detected CRISPR arrays, but also CRISPR array candidates not detected by other tools. Compared to other methods, our tool has a drastically reduced false positive rate. In contrast to the existing tools, our approach not only provides the user with the basic statistics on the identified CRISPR arrays but also produces a certainty score as a practical measure of the likelihood that a given genomic region is a CRISPR array.</description><subject>Clustered Regularly Interspaced Short Palindromic Repeats</subject><subject>Genome, Archaeal</subject><subject>Genome, Bacterial</subject><subject>Machine Learning</subject><subject>Methods Online</subject><subject>Software</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kUlPwzAQhS0EoqVw44xygwOhdrwk5oCEKpZKlYoKnK2p47SGNA52g9R_T6ouggunGc18erM8hM4JviFY0n4Fvj_7BCCEZweoS6hIYiZFcoi6mGIeE8yyDjoJ4QNjwghnx6hDaSIxx7yLxoPJ8PVlYnNTLW2xuo22mdWwtK6KXBFtiAi8h1WImmCrWbQAPbeViUoDvloXoK69a4un6KiAMpizbeyh98eHt8FzPBo_DQf3o1gzIpYx19qAlNoI0JgSnWOdJZixrCBTJkRuGE25FCKROk9lrjnFKQVG2hNEwqeS9tDdRrdupguT63ZpD6WqvV2AXykHVv3tVHauZu5bpZLQVNBW4Gor4N1XY8JSLWzQpiyhMq4JKmEiEzyjlLXo9QbV3oXgTbEfQ7Bae6BaD9TOgxa_-L3aHt49vQUuN4Br6v-lfgC8W5D-</recordid><startdate>20210226</startdate><enddate>20210226</enddate><creator>Mitrofanov, Alexander</creator><creator>Alkhnbashi, Omer S</creator><creator>Shmakov, Sergey A</creator><creator>Makarova, Kira S</creator><creator>Koonin, Eugene V</creator><creator>Backofen, Rolf</creator><general>Oxford University Press</general><scope>TOX</scope><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8088-590X</orcidid><orcidid>https://orcid.org/0000-0003-3943-8299</orcidid><orcidid>https://orcid.org/0000-0001-8231-3323</orcidid><orcidid>https://orcid.org/0000-0002-8174-2844</orcidid></search><sort><creationdate>20210226</creationdate><title>CRISPRidentify: identification of CRISPR arrays using machine learning approach</title><author>Mitrofanov, Alexander ; Alkhnbashi, Omer S ; Shmakov, Sergey A ; Makarova, Kira S ; Koonin, Eugene V ; Backofen, Rolf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-5ccea99ce6ac031cd0c820448f1b466de437596629cd79dc53073a41001625b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Clustered Regularly Interspaced Short Palindromic Repeats</topic><topic>Genome, Archaeal</topic><topic>Genome, Bacterial</topic><topic>Machine Learning</topic><topic>Methods Online</topic><topic>Software</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitrofanov, Alexander</creatorcontrib><creatorcontrib>Alkhnbashi, Omer S</creatorcontrib><creatorcontrib>Shmakov, Sergey A</creatorcontrib><creatorcontrib>Makarova, Kira S</creatorcontrib><creatorcontrib>Koonin, Eugene V</creatorcontrib><creatorcontrib>Backofen, Rolf</creatorcontrib><collection>Oxford University Press Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitrofanov, Alexander</au><au>Alkhnbashi, Omer S</au><au>Shmakov, Sergey A</au><au>Makarova, Kira S</au><au>Koonin, Eugene V</au><au>Backofen, Rolf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CRISPRidentify: identification of CRISPR arrays using machine learning approach</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2021-02-26</date><risdate>2021</risdate><volume>49</volume><issue>4</issue><spage>e20</spage><epage>e20</epage><pages>e20-e20</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
CRISPR–Cas are adaptive immune systems that degrade foreign genetic elements in archaea and bacteria. In carrying out their immune functions, CRISPR–Cas systems heavily rely on RNA components. These CRISPR (cr) RNAs are repeat-spacer units that are produced by processing of pre-crRNA, the transcript of CRISPR arrays, and guide Cas protein(s) to the cognate invading nucleic acids, enabling their destruction. Several bioinformatics tools have been developed to detect CRISPR arrays based solely on DNA sequences, but all these tools employ the same strategy of looking for repetitive patterns, which might correspond to CRISPR array repeats. The identified patterns are evaluated using a fixed, built-in scoring function, and arrays exceeding a cut-off value are reported. Here, we instead introduce a data-driven approach that uses machine learning to detect and differentiate true CRISPR arrays from false ones based on several features. Our CRISPR detection tool, CRISPRidentify, performs three steps: detection, feature extraction and classification based on manually curated sets of positive and negative examples of CRISPR arrays. The identified CRISPR arrays are then reported to the user accompanied by detailed annotation. We demonstrate that our approach identifies not only previously detected CRISPR arrays, but also CRISPR array candidates not detected by other tools. Compared to other methods, our tool has a drastically reduced false positive rate. In contrast to the existing tools, our approach not only provides the user with the basic statistics on the identified CRISPR arrays but also produces a certainty score as a practical measure of the likelihood that a given genomic region is a CRISPR array.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>33290505</pmid><doi>10.1093/nar/gkaa1158</doi><orcidid>https://orcid.org/0000-0001-8088-590X</orcidid><orcidid>https://orcid.org/0000-0003-3943-8299</orcidid><orcidid>https://orcid.org/0000-0001-8231-3323</orcidid><orcidid>https://orcid.org/0000-0002-8174-2844</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Clustered Regularly Interspaced Short Palindromic Repeats Genome, Archaeal Genome, Bacterial Machine Learning Methods Online Software |
title | CRISPRidentify: identification of CRISPR arrays using machine learning approach |
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