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Rathod, Y.

Publications and source records attributed to Rathod, Y..

2 recordsLinked to original sources

Muon Reduces the Training Cost of Regulatory DNA Transformers

Gene-therapy design depends on identifying regulatory sequences that drive the right level, timing, and cell-type specificity of expression. Regulatory DNA models offer a way to prioritize such sequences computationally before committing candidates to biological testing. Biological validation involves DNA synthesis, cloning, cell culture, sequencing, and functional screening, so training compute is part of the same constrained discovery pipeline rather than an isolated modeling expense. Reducing the compute required to reach a target pretraining quality could shift time and budget toward larger candidate screens, additional assays, more cell contexts, and broader follow-up validation. Given that Adam-style optimizers are widely used for training genomic sequence models, we study whether Muon can provide a more compute-efficient alternative for regulatory DNA pretraining. We provide an in-depth analysis by training Transformer models (26M-420M parameters) on ENCODE cis-regulatory sequences with Adam and Muon while holding architecture, data, and non-optimizer hyperparameters fixed and varying optimizer family, norm-control scheme, learning rate, and model width. In the largest-scale matched-target comparison, Muon reaches Adam-matched perplexity targets with a median FLOP reduction of 35.4% and a median wall-clock time reduction of 38.5%. The analysis further shows that optimizer rankings depend on norm control: independent weight decay pairs more favorably with Muon than Hyperball in this setting. These findings indicate that optimizer update structure and norm-control choices are practical levers for reducing the training resources required to reach matched perplexity targets in regulatory DNA pretraining.

genomics↗

Identification of Prospective PETases Across Prokaryotes Using an in silico Approach

BackgroundPlastics count as one of the most potent threats to the habitats and survival of global flora and fauna. Reports keep accumulating globally about the ever-exploding load of plastic wastes, but the need and economics of multiple industrial and household processes compels the production of more plastic materials. It has always been imperative to look for natural sources of degradation of plastic. The identification of plastic-degrading microbes, therefore remains a major focus of the microbial fraternity. While the discoveries of Ideonella sakaiensis or later, Rhizobacter gummiphilus were more out of providence, the structure determination of the enzyme responsible for PET degradation does provide a fillip to efforts towards identification of more such prokaryotic entities. ResultsIn this work, a comprehensive profiling of prokaryotic sequences has been undertaken to look for the presence of similar plastic-degradation abilities across the kingdom. The identification of twenty-seven such hits across different bacterial species led us to believe in the natural diversity of plastic-degradation enzymes. Moreover, there seems to be conservation of the structural motif that renders such ability as has been observed from the constructed models and analysis of their interfaces. Docking of BHET, one of the key products of PET, against these 27 entities showed considerable interactions with the above and pointed towards the possible roles of these bacteria as natural plastic degradation models. Eight of these proteins have very close similarity in binding interactions and surface properties to the PETase from I. sakaiensis and were shortlisted as prospective candidates. ConclusionsOf these eight, three PETases from Halopseudomonas pertucinogena Halopseudomonas bauzanensis and Ketobacter sp. revealed significant similarity in structure and conformational stability to the PETase from I. sakaiensis as was evident from the analysis of their molecular dynamics parameters. Principal Component Analysis and the free energy landscape during binding to BHET also validated the hypothesis and these three PETases could be immediately explored for possible plastic degradation activity.

bioinformatics↗