<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Coughlin DJ</submitter><funding>NIGMS NIH HHS</funding><funding>CIHR</funding><pagination>195-202</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2783191</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Transfer RNA (tRNA) gene predictions are complicated by challenges such as structural variation, limited sequence conservation and the presence of highly reiterated short interspersed sequences (SINEs) that originally derived from tRNA genes or tRNA-like transcription units. Annotation of "tRNA genes" in sequenced genomes generally have not been accompanied by experimental verification of the expression status of predicted sequences.&lt;h4>Results&lt;/h4>To address this for mouse tRNA genes, we have employed two programs, tRNAScan-SE and ARAGORN, to predict the tRNA genes in the nuclear genome, resulting in diverse but overlapping predicted gene sets. From these, we removed known SINE repeats and sorted the genes into predicted families and single-copy genes. In particular, fo</pubmed_abstract><journal>RNA biology</journal><pubmed_title>Prediction and verification of mouse tRNA gene families.</pubmed_title><pmcid>PMC2783191</pmcid><funding_grant_id>R01 GM082875</funding_grant_id><funding_grant_id>R01 GM034869</funding_grant_id><funding_grant_id>GM082875</funding_grant_id><funding_grant_id>MOP-49451</funding_grant_id><funding_grant_id>T32 GM007767</funding_grant_id><pubmed_authors>Engelke DR</pubmed_authors><pubmed_authors>Hughes TR</pubmed_authors><pubmed_authors>Babak T</pubmed_authors><pubmed_authors>Nihranz C</pubmed_authors><pubmed_authors>Coughlin DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction and verification of mouse tRNA gene families.</name><description>&lt;h4>Background&lt;/h4>Transfer RNA (tRNA) gene predictions are complicated by challenges such as structural variation, limited sequence conservation and the presence of highly reiterated short interspersed sequences (SINEs) that originally derived from tRNA genes or tRNA-like transcription units. Annotation of "tRNA genes" in sequenced genomes generally have not been accompanied by experimental verification of the expression status of predicted sequences.&lt;h4>Results&lt;/h4>To address this for mouse tRNA genes, we have employed two programs, tRNAScan-SE and ARAGORN, to predict the tRNA genes in the nuclear genome, resulting in diverse but overlapping predicted gene sets. From these, we removed known SINE repeats and sorted the genes into predicted families and single-copy genes. In particular, fo</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Apr-Jun</publication><modification>2026-05-02T23:39:10.853Z</modification><creation>2026-04-07T18:37:15.717Z</creation></dates><accession>S-EPMC2783191</accession><cross_references><pubmed>19246989</pubmed><doi>10.4161/rna.6.2.8050</doi></cross_references></HashMap>