Although we now have a rich toolset for genome editing, an equivalent framework for manipulating the proteome with a comparable flexibility and specificity remains elusive. A promising strategy for “proteome editing” is to use bifunctional molecules ...
Understanding whole-brain circuitry development is essential for uncovering the origins of disorders linked to abnormal neural wiring, yet progress has been limited by the lack of tools for accurate, comprehensive analysis. Brain development is highl...
The discovery of therapeutic antibodies is a traditionally arduous process. Today, the lab-based process of antibody discovery consists of several time-consuming steps that involve live animal immunization, B-cell harvesting, hybridoma creation, and ...
The statistics of correlations are central quantities characterizing the collective dynamics of recurrent neural networks. We derive exact expressions for the statistics of correlations of nonlinear recurrent networks in the limit of a large number N...
Large rare copy number variants (CNVs) are a main source of genetic variation in the genome and are important in both evolution and disease risk. CNVs can be detected using different data sources, including genome sequencing, genotyping arrays and qu...
Identifying protein binding sites is central to drug discovery, yet many computational approaches still trade off precision, recall, or throughput when scaled. We introduce PickPocket, a deep learning model that fuses evolutionary information from pr...
Attention is a fundamental mechanism enabling the brain to overcome its limited capacity for parallel processing. In non-human primates, invasive electrophysiology has shown that attentional selection operates rhythmically, primarily within the alpha...
Training and deploying large-scale protein language models typically requires deep machine learning expertise — a barrier for researchers outside this field. SaprotHub overcomes this challenge by offering an intuitive platform that facilitates traini...
Thoracic aortic aneurysms (TAAs) arise from a combination of biological and mechanical factors. Current clinical guidelines use size and rate of expansion to stratify risk, but such metrics do not predict if an aneurysm will stabilize, grow, dissect,...
Predicting the transcriptional effects of genetic perturbations across diverse contexts is a central challenge in functional genomics. While single-cell perturbational assays such as Perturb-seq have generated valuable datasets, exhaustively profilin...
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