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de Lima Camillo, L. P.

Publications and source records attributed to de Lima Camillo, L. P..

2 recordsLinked to original sources

pyaging: a Python-based compendium of GPU-optimized aging clocks

MotivationAging is intricately linked to diseases and mortality and is reflected in molecular changes across various tissues. The development and refinement of biomarkers of aging, healthspan, and lifespan using machine learning models, known as aging clocks, leverage epigenetic and other molecular signatures. Despite advancements, as noted by the Biomarkers of Aging Consortium, the field grapples with challenges, notably the lack of robust software tools for integrating and comparing these diverse models. ResultsI introduce pyaging, a comprehensive Python package, designed to bridge the gap in aging research software tools. pyaging integrates over 30 aging clocks, with plans to expand to more than 100, covering a range of molecular data types including DNA methylation, transcriptomics, histone mark ChIP-Seq, and ATAC-Seq. The package features a variety of model types, from linear and principal component models to neural networks and automatic relevance determination models. Utilizing a PyTorch-based backend for GPU acceleration, pyaging ensures rapid inference even with large datasets and complex models. The package supports multi-species analysis, currently including humans, various mammals, and C. elegans. Availability and Implementationpyaging is accessible at https://github.com/rsinghlab/pyaging. The package is structured to facilitate ease of use and integration into existing research workflows, supporting the flexible anndata data format. Supplementary InformationSupplementary materials, including detailed documentation and usage examples, are available online at the pyaging documentation site (https://pyaging.readthedocs.io/en/latest/index.html).

bioinformatics↗

Histone mark age of human tissues and cells

BackgroundAging involves intricate epigenetic changes, with histone modifications playing a pivotal role in dynamically regulating gene expression. Our research comprehensively analyzes seven key histone modifications across various tissues to understand their behavior during human aging and formulate age prediction models. ResultsThese histone-centric prediction models exhibit remarkable accuracy and resilience against experimental and artificial noise. They showcase comparable efficacy when compared with DNA methylation age predictors through simulation experiments. Intriguingly, our gene set enrichment analysis pinpoints vital developmental pathways crucial for age prediction. Unlike in DNA methylation age predictors, genes previously recognized in animal studies as integral to aging are amongst the most important features of our models. We also introduce a pan-histone-mark, pan-tissue age predictor that operates across multiple tissues and histone marks, reinforcing that age-related epigenetic markers are not restricted to particular histone modifications. ConclusionOur findings underscore the potential of histone marks in crafting robust age predictors and shed light on the intricate tapestry of epigenetic alterations in aging.

systems biology↗