eVITTA: a web-based visualization and inference toolbox for transcriptome analysis.
Xuanjin ChengJunran YanYongxing LiuJiahe WangStefan TaubertPublished in: Nucleic acids research (2021)
Transcriptome profiling is essential for gene regulation studies in development and disease. Current web-based tools enable functional characterization of transcriptome data, but most are restricted to applying gene-list-based methods to single datasets, inefficient in leveraging up-to-date and species-specific information, and limited in their visualization options. Additionally, there is no systematic way to explore data stored in the largest transcriptome repository, NCBI GEO. To fill these gaps, we have developed eVITTA (easy Visualization and Inference Toolbox for Transcriptome Analysis; https://tau.cmmt.ubc.ca/eVITTA/). eVITTA provides modules for analysis and exploration of studies published in NCBI GEO (easyGEO), detailed molecular- and systems-level functional profiling (easyGSEA), and customizable comparisons among experimental groups (easyVizR). We tested eVITTA on transcriptomes of SARS-CoV-2 infected human nasopharyngeal swab samples, and identified a downregulation of olfactory signal transducers, in line with the clinical presentation of anosmia in COVID-19 patients. We also analyzed transcriptomes of Caenorhabditis elegans worms with disrupted S-adenosylmethionine metabolism, confirming activation of innate immune responses and feedback induction of one-carbon cycle genes. Collectively, eVITTA streamlines complex computational workflows into an accessible interface, thus filling the gap of an end-to-end platform capable of capturing both broad and granular changes in human and model organism transcriptomes.
Keyphrases
- single cell
- rna seq
- sars cov
- immune response
- high throughput
- endothelial cells
- genome wide
- electronic health record
- big data
- cell proliferation
- signaling pathway
- gene expression
- genome wide identification
- toll like receptor
- randomized controlled trial
- dna methylation
- systematic review
- cerebrospinal fluid
- inflammatory response
- ionic liquid
- dendritic cells
- health information
- resting state
- artificial intelligence
- machine learning
- genetic diversity