The discovery rate of optical transients will explode to 10 million public alerts per night once the Vera C. Rubin Observatory’s Legacy Survey of Space and Time comes online, overwhelming the traditional physics-based inference pipelines. A continuous-time forecasting AI model is of interest because it can deliver millisecond-scale inference for thousands of objects per day, whereas legacy MCMC codes need hours per object. In this paper, we propose SELDON, a new continuous-time variational autoencoder for panels of sparse and irregularly time-sampled (gappy) astrophysical light curves that are nonstationary, heteroscedastic, and inherently dependent. SELDON combines a masked GRU-ODE encoder with a latent neural ODE propagator and an interpretable Gaussian-basis decoder. The encoder learns to summarize panels of imbalanced and correlated data even when only a handful of points are observed. The neural ODE then integrates this hidden state forward in continuous time, extrapolating to future unseen epochs. This extrapolated time series is further encoded by deep sets to a latent distribution that is decoded to a weighted sum of Gaussian basis functions, the parameters of which are physically meaningful. Such parameters (e.g., rise time, decay rate, peak flux) directly drive downstream prioritization of spectroscopic follow-up for astrophysical surveys. Beyond astronomy, the architecture of SELDON offers a generic recipe for interpretable and continuous-time sequence modeling in any time domain where data are multivariate, sparse, heteroscedastic, and irregularly spaced.

BACKGROUND: The variant call format (VCF) file is a structured and comprehensive text file crucial for researchers and clinicians in interpreting and understanding genomic variation data. It contains essential information about variant positions in the genome, along with alleles, genotype calls, and quality scores. Analyzing and visualizing these files, however, poses significant challenges due to the need for diverse resources and robust features for in-depth exploration. RESULTS: To address these challenges, we introduce variant graph craft (VGC), a VCF file visualization and analysis tool. VGC offers a wide range of features for exploring genetic variations, including extraction of variant data, intuitive visualization, and graphical representation of samples with genotype information. VGC is designed primarily for the analysis of patient cohorts, but it can also be adapted for use with individual probands or families. It integrates seamlessly with external resources, providing insights into gene function and variant frequencies in sample data. VGC includes gene function and pathway information from Molecular Signatures Database (MSigDB) for GO terms, KEGG, Biocarta, Pathway Interaction Database, and Reactome. Additionally, it dynamically links to gnomAD for variant information and incorporates ClinVar data for pathogenic variant information. VGC supports the Human Genome Assembly Hg37 and Hg38, ensuring compatibility with a wide range of data sets, and accommodates various approaches to exploring genetic variation data. It can be tailored to specific user needs with optional phenotype input data. CONCLUSIONS: In summary, VGC provides a comprehensive set of features tailored to researchers working with genomic variation data. Its intuitive interface, rapid filtering capabilities, and the flexibility to perform queries using custom groups make it an effective tool in identifying variants potentially associated with diseases. VGC operates locally, ensuring data security and privacy by eliminating the need for cloud-based VCF uploads, making it a secure and user-friendly tool. It is freely available at https://github.com/alperuzun/VGC .