Generative model designs working disordered protein segments from scratch
A biophysical generative algorithm designed functional intrinsically disordered regions from scratch for the developmental transcription factor RUNX2.
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Thursday, October 15, 2026Thu, Oct 15
Updated 5:32 PM PT
A biophysical generative algorithm designed functional intrinsically disordered regions from scratch for the developmental transcription factor RUNX2.
Researchers built CellChain, an evaluation benchmark spanning 590 biological cases and 2,360 matched conditions across gene dependency, cytokine signaling, and drug sensitivity.
Researchers introduced an optimization and Bayesian inference framework that penalizes parameter sets violating thermodynamic detailed balance, rather than strictly reparameterizing complex reaction networks.
Computational biologists introduced NetMap, a software pipeline that jointly infers single-cell gene regulatory networks and clusters cell populations without needing pre-assigned cell annotations.
Genentech researchers developed CellMAPP and an analytical framework called CHART to track organelle changes across 524 genetic knockdowns in breast cancer cells.
Researchers built LabCompass, an active-learning system that pairs a flow-matching generative model with a surrogate predictor to design continuous chemical recipes that push stem cells toward specific fates.
Researchers combined two-dimensional melanoma cell cultures with mechanical particle simulations to study how spatial crowding drives drug-resistant tumor cells to break free.
Researchers introduced MD-LLM-2, a transferable language model that generates protein motion trajectories conditioned on sequence, temperature, and structural history.
Researchers introduced latent causal diffusion (LCD), a generative diffusion framework designed to model single-cell perturbation responses while accounting for measurement noise.
The Chan Zuckerberg Biohub has unveiled an expanded $1.8 billion Virtual Biology Initiative in collaboration with Meta, Google DeepMind, Isomorphic Labs, the Department of Energy, and the National Institutes of Health.
CardamomOT combines optimal transport mathematics with a mechanistic model of gene expression to infer gene regulatory networks and reconstruct unmeasured protein trajectories across single-cell RNA sequencing time series.
A computational framework called scBOLT simplifies the process of turning single-cell RNA sequencing data across multiple experimental conditions into Boolean logic models of gene regulation.
Researchers introduced scEGFlow, a framework combining conditional flow matching with energy guidance to model how individual cells shift in appearance and gene expression following biological perturbations.
Computational biologists developed SCITRAM, a desktop tool that infers gene regulatory networks from single-cell RNA sequencing and simulates transcription factor activation cascades to identify master control proteins.
OmniVCBench introduces 6,077 question-and-answer pairs based on published figures to evaluate whether multimodal AI models can interpret wet-lab data and formulate biological hypotheses.
KoopCell uses dynamical systems theory to infer cell development over time from unpaired single-cell RNA sequencing snapshots.
A team created GEMOT, an AI agent framework designed to infer explicit, modular mathematical equations and hidden biological states from sparse experimental data.
Researchers introduced SHERLOCK, a deep generative model that treats single-cell genetic and drug perturbations as structured interventions on a baseline cellular state within a causal framework.
An automated modeling pipeline uses biophysical simulations of neurons to identify how adjusting normal ion channels can restore healthy firing patterns without directly targeting the mutated channel.
DeepSCENIC transfers representations from sequence-to-function deep learning models, such as Enformer and Borzoi, to single-cell multiomic atlases to reconstruct causal gene regulatory networks.
StressNET, a graph neural network, estimates physical forces between neighboring cells directly from microscopy images without relying on pre-specified physical formulas.
Computational biologists developed SPHERE-PCA, a method that maps the first three principal components of single-cell RNA sequencing data onto a three-dimensional unit sphere to create an interpretable coordinate framework.
Researchers built CELL-FM, a bidirectional generative AI framework that predicts fluorescence microscopy images directly from protein sequences and cellular context, and can also work in reverse.
Researchers built a mechanistic computational model combining chromatin dynamics, in vitro response data, and drug distribution kinetics to simulate how triple-negative breast cancer responds to combination epigenetic therapy.
Therna Biosciences has released public datasets from its Chronos platform profiling roughly 60,000 synthetic regulatory elements across approximately 50 pooled cell lines.
Computational biologists introduced PHAROS, an algorithmic framework that chains predictions from existing single-cell perturbation models to simulate and search for synergistic two-drug combinations.
A systematic evaluation of 13 computational methods across 25 perturbation datasets found that current models struggle to generalize cellular drug and gene responses across different cell types.
Scientists developed ProteinTalks, an operational virtual cell model pretrained on more than 38 million time-resolved protein abundance measurements from perturbed breast cancer cell lines.
The computational tool IRIS uses transfer learning to infer in vivo signaling dynamics and cellular histories from single-cell gene expression atlases.