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Bolzan, D.

Publications and source records attributed to Bolzan, D..

2 recordsLinked to original sources

Soffritto: a deep-learning model for predicting high-resolution replication timing

MotivationReplication Timing (RT) refers to the order by which DNA loci are replicated during S phase. RT is cell-type specific and implicated in cellular processes including transcription, differentiation, and disease. RT is typically quantified genome-wide using two-fraction assays (e.g., Repli-Seq) which sort cells into early and late S phase fractions followed by DNA sequencing yielding a ratio as the RT signal. While two-fraction RT data is widely available in multiple cell lines, it is limited in its ability to capture high-resolution RT features. To address this, high-resolution Repli-Seq, which quantifies RT across 16 fractions, was developed, but it is costly and technically challenging with very limited data generated to date. ResultsHere we developed Soffritto, a deep learning model that predicts high-resolution RT data using two-fraction RT data, histone ChIP-seq data, GC content, and gene density as input. Soffritto is composed of a Long Short Term Memory (LSTM) module and a prediction module. The LSTM module learns long- and short-range interactions between genomic bins while the prediction module is composed of a fully connected layer that outputs a 16-fraction probability vector for each bin using the LSTM modules embeddings as input. By performing both within cell line and cross cell line training and testing for five human and mouse cell lines, we show that Soffritto is able to capture experimental 16-fraction RT signals with high accuracy and the predicted signals allow detection of high-resolution RT patterns. AvailabilitySoffritto is available at https://github.com/ay-lab/Soffritto.

bioinformatics↗

A multi-tiered map of EMT defines major transition points and identifies vulnerabilities

Epithelial to mesenchymal transition (EMT) is a complex cellular program proceeding through a hybrid E/M state linked to cancer-associated stemness, migration and chemoresistance. Deeper molecular understanding of this dynamic physiological landscape is needed to define events which regulate the transition and entry into and exit from the E/M state. Here, we quantified >60,000 molecules across ten time points and twelve omic layers in human mammary epithelial cells undergoing TGF{beta}-induced EMT. Deep proteomic profiles of whole cells, nuclei, extracellular vesicles, secretome, membrane and phosphoproteome defined state-specific signatures and major transition points. Parallel metabolomics showed metabolic reprogramming preceded changes in other layers, while single-cell RNA sequencing identified transcription factors controlling entry into E/M. Covariance analysis exposed unexpected discordance between the molecular layers. Integrative causal modeling revealed co-dependencies governing entry into E/M that were verified experimentally using combinatorial inhibition. Overall, this dataset provides an unprecedented resource on TGF{beta} signaling, EMT and cancer.

systems biology↗