Tangerine: A Python framework for dynamic gene regulation analysis from transcriptomic time series
Narendra, T.; Schweikert, G.
Show abstract
MotivationTime-series single-cell transcriptomics enables the study of dynamic gene regulation. However, standard computational tools frequently aggregate temporal data into static, dense topologies, obscuring the precise regulatory rewiring that drives developmental transitions. Further, navigating the inherent noise of statistical inference without losing biological interpretability remains an important bottleneck. ResultsWe present Tangerine, a Python framework for the dynamic reconstruction and interactive exploration of time-varying gene regulatory networks. Tangerine integrates time-constrained metacell aggregation with regularized linear modelling and non-parametric correlation to infer dynamic topologies. To solve the interpretability gap, it features a browser-based visual analytics engine. Tangerine empowers researchers to track macroscopic gene module evolution, interactively filter effect sizes, and link topological rewiring directly to raw transcriptomic evidence. Availability and implementationTangerine is implemented in Python and Plotly Dash. The code is available on Github at https://github.com/ntanmayee/tangerine.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- High performance single-cell gene regulatory network inference at scale: The Inferelator 3.0 95%
- Non-negative Independent Factor Analysis disentangles discrete and continuous sources of variation in scRNA-seq data 94%
- AdaLiftOver: High-resolution identification of orthologous regulatory elements with adaptive liftOver 94%
Similar papers in this journal
Similar papers in this journal
- A scalable computational framework for predicting gene expression from candidate cis-regulatory elements 94%
- Automated quality control and cell identification of droplet-based single-cell data using dropkick 93%
- Learning probabilistic protein-DNA recognition codes from DNA-binding specificities using structural mappings 93%
"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.