<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu H</submitter><funding>Ningbo Top Medical and Health Research Program</funding><funding>Project of National Key Clinical Specialty</funding><funding>Ningbo Leading Medical&amp;Health Discipline</funding><funding>National Natural Science Foundation of China</funding><pagination>D239-D246</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12807645</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(D1)</volume><pubmed_abstract>The rapid advancement of single-cell multi-omics technologies, typified by single-cell RNA sequencing (scRNA-seq), has provided systematic methodologies for dissecting gene expression heterogeneity within cell populations. However, long noncoding RNAs (lncRNAs) research is hindered by a lack of databases covering diverse tissues, disease contexts, and integrated multi-dimensional single-cell annotations. To address this gap, we updated NONCODE v7.0 (available at https://v7.noncode.org/) through the integration of scRNA-seq data, enabling systematic analysis of lncRNA expression. NONCODE v7.0 incorporates 2061 human scRNA-seq samples from 229 datasets, covering a spectrum of 6 categories, with 3 core ones including Physiological Control as an immune baseline, Physiological Development, and </pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>NONCODE v7.0: updated lncRNA resource integrating scRNA-seq data encompassing immune baseline, development, and disease.</pubmed_title><pmcid>PMC12807645</pmcid><funding_grant_id>92474204</funding_grant_id><funding_grant_id>2022-S02</funding_grant_id><funding_grant_id>2023030615</funding_grant_id><funding_grant_id>2024017</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Fan Y</pubmed_authors><pubmed_authors>Le X</pubmed_authors><pubmed_authors>Gao K</pubmed_authors><pubmed_authors>Zeng X</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>NONCODE v7.0: updated lncRNA resource integrating scRNA-seq data encompassing immune baseline, development, and disease.</name><description>The rapid advancement of single-cell multi-omics technologies, typified by single-cell RNA sequencing (scRNA-seq), has provided systematic methodologies for dissecting gene expression heterogeneity within cell populations. However, long noncoding RNAs (lncRNAs) research is hindered by a lack of databases covering diverse tissues, disease contexts, and integrated multi-dimensional single-cell annotations. To address this gap, we updated NONCODE v7.0 (available at https://v7.noncode.org/) through the integration of scRNA-seq data, enabling systematic analysis of lncRNA expression. NONCODE v7.0 incorporates 2061 human scRNA-seq samples from 229 datasets, covering a spectrum of 6 categories, with 3 core ones including Physiological Control as an immune baseline, Physiological Development, and </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-02T03:16:11.05Z</modification><creation>2026-06-02T03:10:41.105Z</creation></dates><accession>S-EPMC12807645</accession><cross_references><pubmed>41261731</pubmed><doi>10.1093/nar/gkaf1132</doi></cross_references></HashMap>