<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bickhart DM</submitter><funding>USDA-ARS</funding><pagination>gigabyte42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9650271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2022</volume><pubmed_abstract>Relative to other crops, red clover (&lt;i>Trifolium pratense&lt;/i> L.) has various favorable traits making it an ideal forage crop. Conventional breeding has improved varieties, but modern genomic methods could accelerate progress and facilitate gene discovery. Existing short-read-based genome assemblies of the ∼420 megabase pair (Mbp) genome are fragmented into >135,000 contigs, with numerous order and orientation errors within scaffolds, probably associated with the plant's biology, which displays gametophytic self-incompatibility resulting in inherent high heterozygosity. Here, we present a high-quality long-read-based assembly of red clover with a more than 500-fold reduction in contigs, improved per-base quality, and increased contig N50 by three orders of magnitude. The 413.5 Mbp assembly is nearly 20% longer than the 350 Mbp short-read assembly, closer to the predicted genome size. We also present quality measures and full-length isoform RNA transcript sequences for assessing accuracy and future genome annotation. The assembly accurately represents the seven main linkage groups in an allogamous (outcrossing), highly heterozygous plant genome.</pubmed_abstract><journal>GigaByte (Hong Kong, China)</journal><pubmed_title>Chromosome-scale assembly of the highly heterozygous genome of red clover (&lt;i>Trifolium pratense&lt;/i> L.), an allogamous forage crop species.</pubmed_title><pmcid>PMC9650271</pmcid><funding_grant_id>3040-31000-100-00D</funding_grant_id><funding_grant_id>5090-21000-071-00D</funding_grant_id><funding_grant_id>5090-21000-001-00D</funding_grant_id><funding_grant_id>5090-31000-026-00D</funding_grant_id><pubmed_authors>Sullivan ML</pubmed_authors><pubmed_authors>Riday H</pubmed_authors><pubmed_authors>Koch LM</pubmed_authors><pubmed_authors>Smith TPL</pubmed_authors><pubmed_authors>Bickhart DM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chromosome-scale assembly of the highly heterozygous genome of red clover (&lt;i>Trifolium pratense&lt;/i> L.), an allogamous forage crop species.</name><description>Relative to other crops, red clover (&lt;i>Trifolium pratense&lt;/i> L.) has various favorable traits making it an ideal forage crop. Conventional breeding has improved varieties, but modern genomic methods could accelerate progress and facilitate gene discovery. Existing short-read-based genome assemblies of the ∼420 megabase pair (Mbp) genome are fragmented into >135,000 contigs, with numerous order and orientation errors within scaffolds, probably associated with the plant's biology, which displays gametophytic self-incompatibility resulting in inherent high heterozygosity. Here, we present a high-quality long-read-based assembly of red clover with a more than 500-fold reduction in contigs, improved per-base quality, and increased contig N50 by three orders of magnitude. The 413.5 Mbp assembly is nearly 20% longer than the 350 Mbp short-read assembly, closer to the predicted genome size. We also present quality measures and full-length isoform RNA transcript sequences for assessing accuracy and future genome annotation. The assembly accurately represents the seven main linkage groups in an allogamous (outcrossing), highly heterozygous plant genome.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T14:17:53.803Z</modification><creation>2025-02-19T02:24:08.269Z</creation></dates><accession>S-EPMC9650271</accession><cross_references><pubmed>36824517</pubmed><doi>10.46471/gigabyte.42</doi></cross_references></HashMap>