Evidence map›Paper›PMID 42627343›Full record

ArticleBioinformatics (Oxford, England)2026

Base-pair resolution conservation data improves cell type specific sequence-to-expression prediction.

Pooja Kathail, Forest Yang, Gabriel B Loeb, Nilah M Ioannidis

Abstract read
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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Pooja KathailCenter for Computational Biology, University of California, Berkeley, Berkeley, CA 94720, United States.
Forest YangHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Gabriel B LoebDivision of Nephrology, Department of Medicine, Institute for Human Genetics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, United States.
Nilah M IoannidisCenter for Computational Biology, University of California, Berkeley, Berkeley, CA 94720, United States.ORCID 0000-0001-9628-8229

Funding

Regulation of GLIS3, a Ciliary Transcription Factor that Prevents Kidney CystsK08DK143339 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Gabriel B Loeb · 2025 to 2026
$351k
NIDDK NIH HHS K08 DK143339UC Noyce Initiative for Computational Transformation, and KidneyCureU.S. National Institutes of Health K08DK143339
6 · The paper itself

Abstract

motivationGenomic sequence-to-activity models can decipher gene regulatory mechanisms and predict the functional impact of regulatory variants. However, current models struggle to integrate information from sequences outside promoters, especially information from cell type specific regulatory elements.

resultsHere, we propose incorporating base-pair resolution evolutionary conservation data into genomic sequence-to-expression predictors. We explore two training strategies-training from scratch or fine-tuning an existing sequence-only model with additional conservation input. We find that in both cases, base-pair resolution conservation data improves cell type specific sequence-to-expression prediction, with training from scratch yielding the greatest benefit. The improvement in cell type specific expression prediction can be attributed in part to the fact that models trained on sequence and conservation data learn to better recognize cell type specific regulatory elements than models trained on sequence alone. AVAILABILITY: Code is available at https://github.com/ni-lab/basenji-phyloP.

Indexed as

Computational BiologyConserved SequenceGenomicsBase PairingSequence Analysis, DNA

Identifiers

PMID42627343
PMCPMC13574364

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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.