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Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species
Next-generation sequencing technologies rely on high quality DNA that is suitable for library preparation followed by sequencing. Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction method...
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Published in: | Plant methods 2014-06, Vol.10 (1), p.21-21 |
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creator | Healey, Adam Furtado, Agnelo Cooper, Tal Henry, Robert J |
description | Next-generation sequencing technologies rely on high quality DNA that is suitable for library preparation followed by sequencing. Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction methods exist that contend with the presence of phenolics and polysaccharides, these methods rely on long incubations, multiple precipitations or commercially available kits to produce high molecular weight and contaminant-free DNA. In this protocol, we describe simple modifications to the established CTAB- based extraction method that allows for reliable isolation of high molecular weight genomic DNA from difficult to isolate plant species Corymbia (a eucalypt) and Coffea (coffee). The simplified protocol does not require multiple clean up steps or commercial based kits, and the isolated DNA passed stringent quality control standards for whole genome sequencing on Illumina HiSeq and TruSeq sequencing platforms. |
doi_str_mv | 10.1186/1746-4811-10-21 |
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Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction methods exist that contend with the presence of phenolics and polysaccharides, these methods rely on long incubations, multiple precipitations or commercially available kits to produce high molecular weight and contaminant-free DNA. In this protocol, we describe simple modifications to the established CTAB- based extraction method that allows for reliable isolation of high molecular weight genomic DNA from difficult to isolate plant species Corymbia (a eucalypt) and Coffea (coffee). The simplified protocol does not require multiple clean up steps or commercial based kits, and the isolated DNA passed stringent quality control standards for whole genome sequencing on Illumina HiSeq and TruSeq sequencing platforms.</description><identifier>ISSN: 1746-4811</identifier><identifier>EISSN: 1746-4811</identifier><identifier>DOI: 10.1186/1746-4811-10-21</identifier><identifier>PMID: 25053969</identifier><language>eng</language><publisher>England: Springer-Verlag</publisher><subject>Analysis ; Coffea ; Corymbia ; DNA ; DNA sequencing ; Eucalyptus ; genome ; high-throughput nucleotide sequencing ; leaves ; Methodology ; Methods ; molecular weight ; Nucleotide sequencing ; phenolic compounds ; Polysaccharides ; quality control ; Quality management ; recalcitrant species</subject><ispartof>Plant methods, 2014-06, Vol.10 (1), p.21-21</ispartof><rights>COPYRIGHT 2014 BioMed Central Ltd.</rights><rights>Copyright © 2014 Healey et al.; licensee BioMed Central Ltd. 2014 Healey et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b709t-9d256922c912f732c74e22822293aaf5d876987034b773820026a2c8105bf8e93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105509/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105509/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,36990,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25053969$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Healey, Adam</creatorcontrib><creatorcontrib>Furtado, Agnelo</creatorcontrib><creatorcontrib>Cooper, Tal</creatorcontrib><creatorcontrib>Henry, Robert J</creatorcontrib><title>Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species</title><title>Plant methods</title><addtitle>Plant Methods</addtitle><description>Next-generation sequencing technologies rely on high quality DNA that is suitable for library preparation followed by sequencing. Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction methods exist that contend with the presence of phenolics and polysaccharides, these methods rely on long incubations, multiple precipitations or commercially available kits to produce high molecular weight and contaminant-free DNA. In this protocol, we describe simple modifications to the established CTAB- based extraction method that allows for reliable isolation of high molecular weight genomic DNA from difficult to isolate plant species Corymbia (a eucalypt) and Coffea (coffee). The simplified protocol does not require multiple clean up steps or commercial based kits, and the isolated DNA passed stringent quality control standards for whole genome sequencing on Illumina HiSeq and TruSeq sequencing platforms.</description><subject>Analysis</subject><subject>Coffea</subject><subject>Corymbia</subject><subject>DNA</subject><subject>DNA sequencing</subject><subject>Eucalyptus</subject><subject>genome</subject><subject>high-throughput nucleotide sequencing</subject><subject>leaves</subject><subject>Methodology</subject><subject>Methods</subject><subject>molecular weight</subject><subject>Nucleotide sequencing</subject><subject>phenolic compounds</subject><subject>Polysaccharides</subject><subject>quality control</subject><subject>Quality management</subject><subject>recalcitrant species</subject><issn>1746-4811</issn><issn>1746-4811</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkt1v1iAUxhujcXN67Z2SeKMX3YAWKLsweZ1fSxY1zl0TynvaYVrooFX330vT-WZNZhQSIJwfDyfPOVn2lOBDQip-RETJ87IiJCc4p-Retr-7uX_rvJc9ivE7xiWhBX-Y7VGGWSG53M9-fgl-9MZ3x0ijaPuhA9TDeOm3qPEBwa8xaDNa1yKXznkLDoIerXcowtUEzsyhq0l3drxGKep7a9DbTxvUBN-jAEZ3xiYNN6Khm9c4gLEQH2cPGt1FeHKzH2QX7999O_mYn33-cHqyOctrgeWYyy1lXFJqJKGNKKgRJVBaUUploXXDtpXgshK4KGshiopiTLmmpiKY1U0FsjjIXi-6w1T3sDXgUjKdGoLtdbhWXlu1jjh7qVr_Q5VJguFZ4M0iUFv_F4F1xPhezcar2XhFsKIkiby8ySL45FocVW-jgS45An6KinBeMCYqWv4bZRwTLDCu_gNNKUjK2JzAiwVtdQfKusbPdZ1xtWEl5iWRbP778A4qzS2ksnoHjU33qwevVg8SM6Y2afUUozo9_7pmjxbWBB9jgGbnYfJobuY7XHt2u3Y7_k_3JuD5AjTaK90GG9XFOcWE4TRKIXjxGyDw9sk</recordid><startdate>20140627</startdate><enddate>20140627</enddate><creator>Healey, Adam</creator><creator>Furtado, Agnelo</creator><creator>Cooper, Tal</creator><creator>Henry, Robert J</creator><general>Springer-Verlag</general><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7X8</scope><scope>7TM</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20140627</creationdate><title>Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species</title><author>Healey, Adam ; Furtado, Agnelo ; Cooper, Tal ; Henry, Robert J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b709t-9d256922c912f732c74e22822293aaf5d876987034b773820026a2c8105bf8e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analysis</topic><topic>Coffea</topic><topic>Corymbia</topic><topic>DNA</topic><topic>DNA sequencing</topic><topic>Eucalyptus</topic><topic>genome</topic><topic>high-throughput nucleotide sequencing</topic><topic>leaves</topic><topic>Methodology</topic><topic>Methods</topic><topic>molecular weight</topic><topic>Nucleotide sequencing</topic><topic>phenolic compounds</topic><topic>Polysaccharides</topic><topic>quality control</topic><topic>Quality management</topic><topic>recalcitrant species</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Healey, Adam</creatorcontrib><creatorcontrib>Furtado, Agnelo</creatorcontrib><creatorcontrib>Cooper, Tal</creatorcontrib><creatorcontrib>Henry, Robert J</creatorcontrib><collection>AGRIS</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Healey, Adam</au><au>Furtado, Agnelo</au><au>Cooper, Tal</au><au>Henry, Robert J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species</atitle><jtitle>Plant methods</jtitle><addtitle>Plant Methods</addtitle><date>2014-06-27</date><risdate>2014</risdate><volume>10</volume><issue>1</issue><spage>21</spage><epage>21</epage><pages>21-21</pages><issn>1746-4811</issn><eissn>1746-4811</eissn><abstract>Next-generation sequencing technologies rely on high quality DNA that is suitable for library preparation followed by sequencing. Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction methods exist that contend with the presence of phenolics and polysaccharides, these methods rely on long incubations, multiple precipitations or commercially available kits to produce high molecular weight and contaminant-free DNA. In this protocol, we describe simple modifications to the established CTAB- based extraction method that allows for reliable isolation of high molecular weight genomic DNA from difficult to isolate plant species Corymbia (a eucalypt) and Coffea (coffee). The simplified protocol does not require multiple clean up steps or commercial based kits, and the isolated DNA passed stringent quality control standards for whole genome sequencing on Illumina HiSeq and TruSeq sequencing platforms.</abstract><cop>England</cop><pub>Springer-Verlag</pub><pmid>25053969</pmid><doi>10.1186/1746-4811-10-21</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Coffea Corymbia DNA DNA sequencing Eucalyptus genome high-throughput nucleotide sequencing leaves Methodology Methods molecular weight Nucleotide sequencing phenolic compounds Polysaccharides quality control Quality management recalcitrant species |
title | Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species |
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