ePlant: Visualizing and Exploring Multiple Levels of Data for Hypothesis Generation in Plant Biology.

A big challenge in current systems biology research arises when different types of data must be accessed from separate sources and visualized using separate tools. The high cognitive load required to navigate such a workflow is detrimental to hypothesis generation. Accordingly, there is a need for a robust research platform that incorporates all data and provides integrated search, analysis, and visualization features through a single portal. Here, we present ePlant (http://bar.utoronto.ca/eplant), a visual analytic tool for exploring multiple levels of Arabidopsis thaliana data through a zoomable user interface. ePlant connects to several publicly available web services to download genome, proteome, interactome, transcriptome, and 3D molecular structure data for one or more genes or gene products of interest. Data are displayed with a set of visualization tools that are presented using a conceptual hierarchy from big to small, and many of the tools combine information from more than one data type. We describe the development of ePlant in this article and present several examples illustrating its integrative features for hypothesis generation. We also describe the process of deploying ePlant as an "app" on Araport. Building on readily available web services, the code for ePlant is freely available for any other biological species research.

PAN-cODE: COVID-19 forecasting using conditional latent ODEs.

The coronavirus disease 2019 (COVID-19) pandemic has caused millions of deaths around the world and revealed the need for data-driven models of pandemic spread. Accurate pandemic caseload forecasting allows informed policy decisions on the adoption of non-pharmaceutical interventions (NPIs) to reduce disease transmission. Using COVID-19 as an example, we present Pandemic conditional Ordinary Differential Equation (PAN-cODE), a deep learning method to forecast daily increases in pandemic infections and deaths. By using a deep conditional latent variable model, PAN-cODE can generate alternative caseload trajectories based on alternate adoptions of NPIs, allowing stakeholders to make policy decisions in an informed manner. PAN-cODE also allows caseload estimation for regions that are unseen during model training. We demonstrate that, despite using less detailed data and having fully automated training, PAN-cODE's performance is comparable to state-of-the-art methods on 4-week-ahead and 6-week-ahead forecasting. Finally, we highlight the ability of PAN-cODE to generate realistic alternative outcome trajectories on select US regions.

Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig.

The type and genomic context of cancer mutations depend on their causes. These causes have been characterized using signatures that represent mutation types that co-occur in the same tumours. However, it remains unclear how mutation processes change during cancer evolution due to the lack of reliable methods to reconstruct evolutionary trajectories of mutational signature activity. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole-genome sequencing data from 2658 cancers across 38 tumour types, we present TrackSig, a new method that reconstructs these trajectories using optimal, joint segmentation and deconvolution of mutation type and allele frequencies from a single tumour sample. In simulations, we find TrackSig has a 3-5% activity reconstruction error, and 12% false detection rate. It outperforms an aggressive baseline in situations with branching evolution, CNA gain, and neutral mutations. Applied to data from 2658 tumours and 38 cancer types, TrackSig permits pan-cancer insight into evolutionary changes in mutational processes.