<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(2)</volume><submitter>Han Y</submitter><pubmed_abstract>N6-methyladenosine (m⁶A) has been identified in various biological processes and plays important regulatory functions in diverse cells. However, there is still no visualization database for exploring global m⁶A patterns across cell lines. Here we collected all available MeRIP-Seq and m⁶A-CLIP-Seq datasets from public databases and identified 340,950 and 179,201 m⁶A peaks dependent on 23 human and eight mouse cell lines respectively. Those m⁶A peaks were further classified into mRNA and lncRNA groups. To better understand the potential function of m⁶A, we then mapped m⁶A peaks in different subcellular components and gene regions. Among those human m⁶A modification, 190,050 and 150,900 peaks were identified in cancer and non-cancer cells, respectively. Finally, all results were integrated an</pubmed_abstract><journal>Cells</journal><pagination>E168</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6406471</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CVm6A: A Visualization and Exploration Database for m⁶As in Cell Lines.</pubmed_title><pmcid>PMC6406471</pmcid><pubmed_authors>He C</pubmed_authors><pubmed_authors>Feng J</pubmed_authors><pubmed_authors>Xia L</pubmed_authors><pubmed_authors>Dong X</pubmed_authors><pubmed_authors>Zuo Z</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Miao Y</pubmed_authors><pubmed_authors>Han Y</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors></additional><is_claimable>false</is_claimable><name>CVm6A: A Visualization and Exploration Database for m⁶As in Cell Lines.</name><description>N6-methyladenosine (m⁶A) has been identified in various biological processes and plays important regulatory functions in diverse cells. However, there is still no visualization database for exploring global m⁶A patterns across cell lines. Here we collected all available MeRIP-Seq and m⁶A-CLIP-Seq datasets from public databases and identified 340,950 and 179,201 m⁶A peaks dependent on 23 human and eight mouse cell lines respectively. Those m⁶A peaks were further classified into mRNA and lncRNA groups. To better understand the potential function of m⁶A, we then mapped m⁶A peaks in different subcellular components and gene regions. Among those human m⁶A modification, 190,050 and 150,900 peaks were identified in cancer and non-cancer cells, respectively. Finally, all results were integrated an</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2026-04-15T13:24:01.944Z</modification><creation>2025-05-29T21:05:49.388Z</creation></dates><accession>S-EPMC6406471</accession><cross_references><pubmed>30781586</pubmed><doi>10.3390/cells8020168</doi></cross_references></HashMap>