Back

Linkage: an interactive shiny app and R package for linking of DNA regulatory peaks to genes

Liu, Z.; Chen, S.; Li, T.; Zhang, C.; Luo, Y.; Zheng, J.; Lu, Z.; Yang, J.; Xu, S.

2024-04-28 bioinformatics
10.1101/2024.04.24.590756 bioRxiv
Show abstract

SummaryExisting studies have demonstrated that the integration analysis of transcriptomic and epigenomic data can be used to better understand the onset and progression of many diseases, as well as identify new diagnostic and prognostic biomarkers. However, such investigations on large-scale sequencing data remain challenging for researchers or clinicians with limited bioinformatics knowledge. To facilitate the interpretation of gene regulatory landscape, we developed an R Shiny application and R package [Linking of atac-seq to gene expression data (Linkage)] for exploring and visualizing potential cis-regulatory elements (CREs) of genes based on ATAC-seq and RNA-seq data. Linkage offers six modules to systematically identify, annotate, and interpret potential gene regulatory elements from the whole genome step by step. Linkage can provide interactive visualization for the correlation between chromatin accessibility and gene expression. More than that, Linkage identifies transcription factors (TFs) that potentially drive the chromatin changes through identifying TF binding motifs within the CREs and constructing trans-regulatory networks of the target gene set. This powerful tool enables researchers to conduct extensive multiomics integration analysis and generate visually appealing visualizations that effectively highlight the relationship between genes and corresponding regulatory elements. With Linkage, users can obtain publishable results and gain deeper insights into the gene regulatory landscape. Availability and implementation Linkage is freely available as a Shiny web application (https://xulabgdpu.org.cn/linkage) and an R package (https://github.com/XuLab-GDPU/Linkage). The documentation is available at (https://aicplane.github.io/Linkage-tutorial/).

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.