# Co-LncRNA: investigating the lncRNA combinatorial effects in GO annotations and KEGG pathways based on human RNA-Seq data

**Authors:** Zheng Zhao, Jing Bai, Aiwei Wu, Yuan Wang, Jinwen Zhang, Zishan Wang, Yongsheng Li, Juan Xu, Xia Li

PMC · DOI: 10.1093/database/bav082 · Database: The Journal of Biological Databases and Curation · 2015-09-10

## TL;DR

Co-LncRNA is a web tool that helps researchers explore how combinations of long non-coding RNAs affect biological functions and pathways using RNA-Seq data.

## Contribution

The tool introduces a method to analyze the combinatorial effects of lncRNAs on GO annotations and KEGG pathways through co-expressed genes.

## Key findings

- Co-LncRNA identifies co-expressed protein-coding genes of lncRNAs across 241 RNA-Seq datasets.
- The tool enables enrichment analysis of multiple lncRNAs in user-selected datasets to reveal combinatorial effects.
- It provides visual pathway overviews and network displays between lncRNAs and their co-expressed genes.

## Abstract

Long non-coding RNAs (lncRNAs) are emerging as key regulators of diverse biological processes and diseases. However, the combinatorial effects of these molecules in a specific biological function are poorly understood. Identifying co-expressed protein-coding genes of lncRNAs would provide ample insight into lncRNA functions. To facilitate such an effort, we have developed Co-LncRNA, which is a web-based computational tool that allows users to identify GO annotations and KEGG pathways that may be affected by co-expressed protein-coding genes of a single or multiple lncRNAs. LncRNA co-expressed protein-coding genes were first identified in publicly available human RNA-Seq datasets, including 241 datasets across 6560 total individuals representing 28 tissue types/cell lines. Then, the lncRNA combinatorial effects in a given GO annotations or KEGG pathways are taken into account by the simultaneous analysis of multiple lncRNAs in user-selected individual or multiple datasets, which is realized by enrichment analysis. In addition, this software provides a graphical overview of pathways that are modulated by lncRNAs, as well as a specific tool to display the relevant networks between lncRNAs and their co-expressed protein-coding genes. Co-LncRNA also supports users in uploading their own lncRNA and protein-coding gene expression profiles to investigate the lncRNA combinatorial effects. It will be continuously updated with more human RNA-Seq datasets on an annual basis. Taken together, Co-LncRNA provides a web-based application for investigating lncRNA combinatorial effects, which could shed light on their biological roles and could be a valuable resource for this community.

Database URL: http://www.bio-bigdata.com/Co-LncRNA/

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TUG1 (taurine up-regulated 1) [NCBI Gene 55000] {aka LINC00080, NCRNA00080, TI-227H}, MALAT1 (metastasis associated lung adenocarcinoma transcript 1) [NCBI Gene 378938] {aka HCN, LINC00047, NCRNA00047, NEAT2, PRO2853, miPEP-52}
- **Diseases:** lung cancer (MESH:D008175), NSCLC (MESH:D002289), cancer (MESH:D009369), neurological disease (MESH:D020271), lung adenocarcinomas (MESH:D000077192)
- **Chemicals:** poly(A)+ (MESH:D011061)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4565967/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC4565967/full.md

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Source: https://tomesphere.com/paper/PMC4565967