PT - JOURNAL ARTICLE AU - Xiaoyu Zhuo AU - Silas Hsu AU - Deepak Purushotham AU - Samuel Chen AU - Daofeng Li AU - Ting Wang TI - Comparing Genomic and Epigenomic Features across Species Using the WashU Comparative Epigenome Browser AID - 10.1101/2022.11.29.518374 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.11.29.518374 4099 - http://biorxiv.org/content/early/2022/12/02/2022.11.29.518374.short 4100 - http://biorxiv.org/content/early/2022/12/02/2022.11.29.518374.full AB - Genome browsers have become an intuitive and critical tool to visualize and analyze genomic features and data. Conventional genome browsers display data/annotations on a single reference genome/assembly; there are also genomic alignment viewer/browsers that help users visualize alignment, mismatch, and rearrangement between syntenic regions. However, there is a growing need for a comparative epigenome browser that can display genomic and epigenomic datasets across different species and enable users to compare them between syntenic regions. Here, we present the WashU Comparative Epigenome Browser (http://comparativegateway.wustl.edu). It allows users to load functional genomic datasets/annotations mapped to different genomes and display them over syntenic regions simultaneously. The browser also displays genetic differences between the genomes from single nucleotide variants (SNVs) to structural variants (SVs) to visualize the association between epigenomic differences and genetic differences. Instead of anchoring all datasets to the reference genome coordinates, it creates independent coordinates of different genome assemblies to faithfully present features and data mapped to different genomes. It uses a simple, intuitive genome-align track to illustrate the syntenic relationship between different species. It extends the widely used WashU Epigenome Browser infrastructure and can be expanded to support multiple species. This new browser function will greatly facilitate comparative genomic/epigenomic research, as well as support the recent growing needs to directly compare and benchmark the T2T CHM13 assembly and other human genome assemblies.Competing Interest StatementThe authors have declared no competing interest.