<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Prince S</submitter><pubmed_abstract>Mitochondrial genomes-in particular those of fungi-often encode genes with a large number of Group I and Group II introns that are conserved at both the sequence and the RNA structure level. They provide a rich resource for the investigation of intron and gene structure, self- and protein-guided splicing mechanisms, and intron evolution. Yet, the degree of sequence conservation of introns is limited, and the primary sequence differs considerably among the distinct intron sub-groups. It makes intron identification, classification, structural modeling, and the inference of gene models a most challenging and error-prone task-frequently passed on to an "expert" for manual intervention. To reduce the need for manual curation of intron structures and mitochondrial gene models, computational meth</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>866187</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8971849</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Refining Mitochondrial Intron Classification With ERPIN: Identification Based on Conservation of Sequence Plus Secondary Structure Motifs.</pubmed_title><pmcid>PMC8971849</pmcid><pubmed_authors>Prince S</pubmed_authors><pubmed_authors>Sarrasin M</pubmed_authors><pubmed_authors>Rioux P</pubmed_authors><pubmed_authors>Filion-Bienvenue F</pubmed_authors><pubmed_authors>Lang BF</pubmed_authors><pubmed_authors>Munoz C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Refining Mitochondrial Intron Classification With ERPIN: Identification Based on Conservation of Sequence Plus Secondary Structure Motifs.</name><description>Mitochondrial genomes-in particular those of fungi-often encode genes with a large number of Group I and Group II introns that are conserved at both the sequence and the RNA structure level. They provide a rich resource for the investigation of intron and gene structure, self- and protein-guided splicing mechanisms, and intron evolution. Yet, the degree of sequence conservation of introns is limited, and the primary sequence differs considerably among the distinct intron sub-groups. It makes intron identification, classification, structural modeling, and the inference of gene models a most challenging and error-prone task-frequently passed on to an "expert" for manual intervention. To reduce the need for manual curation of intron structures and mitochondrial gene models, computational meth</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T12:57:52.901Z</modification><creation>2025-04-04T12:57:52.901Z</creation></dates><accession>S-EPMC8971849</accession><cross_references><pubmed>35369492</pubmed><doi>10.3389/fmicb.2022.866187</doi></cross_references></HashMap>