<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Munoz-Amatriain M</submitter><funding>NSF Plant Genome Research Program</funding><funding>Office of Science of the US Department of Energy</funding><funding>UC Riverside Agricultural Experiment Station Hatch Project</funding><funding>NSF-ABI</funding><funding>USDA Initiative for Future Agriculture and Food Systems</funding><funding>North American Barley Genome Project</funding><funding>National Program of Sustainability I</funding><funding>USDA-CSREES National Research Initiative (NRI)</funding><funding>BarleyCAP</funding><funding>TriticeaeCAP</funding><pagination>216-27</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5014227</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>84(1)</volume><pubmed_abstract>Barley (Hordeum vulgare L.) possesses a large and highly repetitive genome of 5.1 Gb that has hindered the development of a complete sequence. In 2012, the International Barley Sequencing Consortium released a resource integrating whole-genome shotgun sequences with a physical and genetic framework. However, because only 6278 bacterial artificial chromosome (BACs) in the physical map were sequenced, fine structure was limited. To gain access to the gene-containing portion of the barley genome at high resolution, we identified and sequenced 15 622 BACs representing the minimal tiling path of 72 052 physical-mapped gene-bearing BACs. This generated ~1.7 Gb of genomic sequence containing an estimated 2/3 of all Morex barley genes. Exploration of these sequenced BACs revealed that although dis</pubmed_abstract><journal>The Plant journal : for cell and molecular biology</journal><pubmed_title>Sequencing of 15 622 gene-bearing BACs clarifies the gene-dense regions of the barley genome.</pubmed_title><pmcid>PMC5014227</pmcid><funding_grant_id>CA-R-BPS-5306-H</funding_grant_id><funding_grant_id>USDA-NIFA 2010-15718-10</funding_grant_id><funding_grant_id>DE-AC02-05CH11231</funding_grant_id><funding_grant_id>USDA-CSREES-NRI 2006-55606-16722</funding_grant_id><funding_grant_id>DBI-0321756</funding_grant_id><funding_grant_id>01-52100-11346</funding_grant_id><funding_grant_id>DBI-1062301</funding_grant_id><funding_grant_id>LO1204</funding_grant_id><funding_grant_id>2002-35300-12548</funding_grant_id><funding_grant_id>USDA-AFRI-NIFA 2009-85606-05701</funding_grant_id><funding_grant_id>USDA-AFRI-NIFA 2009-65300-05645</funding_grant_id><funding_grant_id>USDA-CSREES 2001-34213-10511</funding_grant_id><pubmed_authors>Cooper L</pubmed_authors><pubmed_authors>Dilbirligi M</pubmed_authors><pubmed_authors>Heinen S</pubmed_authors><pubmed_authors>Bozdag S</pubmed_authors><pubmed_authors>Simkova H</pubmed_authors><pubmed_authors>Dolezel J</pubmed_authors><pubmed_authors>Madishetty K</pubmed_authors><pubmed_authors>Kleinhofs A</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Muehlbauer GJ</pubmed_authors><pubmed_authors>Moscou MJ</pubmed_authors><pubmed_authors>Schmutz J</pubmed_authors><pubmed_authors>Condamine P</pubmed_authors><pubmed_authors>Mirebrahim H</pubmed_authors><pubmed_authors>Beccuti M</pubmed_authors><pubmed_authors>Bhat PR</pubmed_authors><pubmed_authors>Ounit R</pubmed_authors><pubmed_authors>Graner A</pubmed_authors><pubmed_authors>Lemaux P</pubmed_authors><pubmed_authors>Close TJ</pubmed_authors><pubmed_authors>Duma D</pubmed_authors><pubmed_authors>Falk A</pubmed_authors><pubmed_authors>Lonardi S</pubmed_authors><pubmed_authors>Resnik J</pubmed_authors><pubmed_authors>Feiz L</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Rodriguez E</pubmed_authors><pubmed_authors>Jiang T</pubmed_authors><pubmed_authors>Stein N</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Wanamaker S</pubmed_authors><pubmed_authors>Chao S</pubmed_authors><pubmed_authors>Grimwood J</pubmed_authors><pubmed_authors>Alpert M</pubmed_authors><pubmed_authors>Kudrna D</pubmed_authors><pubmed_authors>Hayes PM</pubmed_authors><pubmed_authors>Munoz-Amatriain M</pubmed_authors><pubmed_authors>Svensson JT</pubmed_authors><pubmed_authors>Blake T</pubmed_authors><pubmed_authors>Wing R</pubmed_authors><pubmed_authors>Mammadov J</pubmed_authors><pubmed_authors>Bregitzer P</pubmed_authors><pubmed_authors>Cordero F</pubmed_authors><pubmed_authors>Luo M</pubmed_authors><pubmed_authors>Witt HN</pubmed_authors><pubmed_authors>Wise RP</pubmed_authors><pubmed_authors>Altschmied L</pubmed_authors><pubmed_authors>Gustafson P</pubmed_authors><pubmed_authors>You F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequencing of 15 622 gene-bearing BACs clarifies the gene-dense regions of the barley genome.</name><description>Barley (Hordeum vulgare L.) possesses a large and highly repetitive genome of 5.1 Gb that has hindered the development of a complete sequence. In 2012, the International Barley Sequencing Consortium released a resource integrating whole-genome shotgun sequences with a physical and genetic framework. However, because only 6278 bacterial artificial chromosome (BACs) in the physical map were sequenced, fine structure was limited. To gain access to the gene-containing portion of the barley genome at high resolution, we identified and sequenced 15 622 BACs representing the minimal tiling path of 72 052 physical-mapped gene-bearing BACs. This generated ~1.7 Gb of genomic sequence containing an estimated 2/3 of all Morex barley genes. Exploration of these sequenced BACs revealed that although dis</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Oct</publication><modification>2026-04-30T03:42:33.298Z</modification><creation>2019-03-27T02:23:41Z</creation></dates><accession>S-EPMC5014227</accession><cross_references><pubmed>26252423</pubmed><doi>10.1111/tpj.12959</doi></cross_references></HashMap>