Evidence map›Paper›PMID 40662815›Full record

ArticleBioinformatics (Oxford, England)2025

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

Dante Bolzan, Ferhat Ay

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Dante BolzanCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, CA 92037, United States.ORCID 0000-0002-1004-4213
Ferhat AyCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, CA 92037, United States.ORCID 0000-0002-0708-6914

Funding

Studying the function of human genetic variation in the light of 3D genome organizationR35GM128938 · NIGMS · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Ferhat Ay · 2018 to 2026
$4.6M
NIGMS NIH HHS R35 GM128938NIH HHS R35-GM128938
6 · The paper itself

Abstract

motivationReplication timing (RT) refers to the order in 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 are 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 module's 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. AVAILABILITY AND IMPLEMENTATION: Soffritto is available at https://github.com/ay-lab/Soffritto.

Indexed as

Deep LearningDNA Replication TimingSoftwareAnimalsComputational BiologyHumansSequence Analysis, DNA

Identifiers

PMID40662815
PMCPMC12261407

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.