<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Revil T</submitter><funding>Canadian Institutes of Health Research</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Alternative splicing is known to increase the complexity of mammalian transcriptomes since nearly all mammalian genes express multiple pre-mRNA isoforms. However, our knowledge of the extent and function of alternative splicing in early embryonic development is based mainly on a few isolated examples. High throughput technologies now allow us to study genome-wide alternative splicing during mouse development.&lt;h4>Results&lt;/h4>A genome-wide analysis of alternative isoform expression in embryonic day 8.5, 9.5 and 11.5 mouse embryos and placenta was carried out using a splicing-sensitive exon microarray. We show that alternative splicing and isoform expression is frequent across developmental stages and tissues, and is comparable in frequency to the variation in whole-transcr</pubmed_abstract><journal>BMC genomics</journal><pagination>399</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2898759</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Alternative splicing is frequent during early embryonic development in mouse.</pubmed_title><pmcid>PMC2898759</pmcid><pubmed_authors>Revil T</pubmed_authors><pubmed_authors>Dias C</pubmed_authors><pubmed_authors>Gaffney D</pubmed_authors><pubmed_authors>Jerome-Majewska LA</pubmed_authors><pubmed_authors>Majewski J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alternative splicing is frequent during early embryonic development in mouse.</name><description>&lt;h4>Background&lt;/h4>Alternative splicing is known to increase the complexity of mammalian transcriptomes since nearly all mammalian genes express multiple pre-mRNA isoforms. However, our knowledge of the extent and function of alternative splicing in early embryonic development is based mainly on a few isolated examples. High throughput technologies now allow us to study genome-wide alternative splicing during mouse development.&lt;h4>Results&lt;/h4>A genome-wide analysis of alternative isoform expression in embryonic day 8.5, 9.5 and 11.5 mouse embryos and placenta was carried out using a splicing-sensitive exon microarray. We show that alternative splicing and isoform expression is frequent across developmental stages and tissues, and is comparable in frequency to the variation in whole-transcr</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2026-04-15T03:14:18.412Z</modification><creation>2026-04-15T03:09:32.31Z</creation></dates><accession>S-EPMC2898759</accession><cross_references><pubmed>20573213</pubmed><doi>10.1186/1471-2164-11-399</doi></cross_references></HashMap>