Evidence map›Paper›PMID 41484786›Full record

ArticleAlgorithms for molecular biology : AMB2026

Improving spliced alignment by modeling splice sites with deep learning.

Siying Yang, Neng Huang, Heng Li

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2026. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Siying YangDepartment of Biomedical Informatics, Harvard Medical School, 10 Shattuck St, Boston, MA, 02215, USA.
Neng HuangDepartment of Biomedical Informatics, Harvard Medical School, 10 Shattuck St, Boston, MA, 02215, USA.
Heng LiDepartment of Biomedical Informatics, Harvard Medical School, 10 Shattuck St, Boston, MA, 02215, USA. hli@ds.dfci.harvard.edu.

Funding

Advanced computational methods in analyzing high-throughput sequencing dataR01HG010040 · NHGRI · DANA-FARBER CANCER INST · PI Heng Li · 2018 to 2026
$3.7M
Calling germline and mosaic variants from long genomic and RNA-seq readsR01HG014175 · NHGRI · DANA-FARBER CANCER INST · PI Heng Li · 2025 to 2026
$1.0M
NHGRI NIH HHS R01 HG010040NHGRI NIH HHS R01HG010040NHGRI NIH HHS R01 HG014175
6 · The paper itself

Abstract

motivationSpliced alignment refers to the alignment of messenger RNA (mRNA) or protein sequences to eukaryotic genomes. It plays a critical role in gene annotation and the study of gene functions. Accurate spliced alignment demands sophisticated modeling of splice sites, but current aligners use simple models, which may affect their accuracy given dissimilar sequences.

resultsWe implemented minisplice to learn splice signals with a one-dimensional convolutional neural network (1D-CNN) and trained a model with 7026 parameters for vertebrate and insect genomes. It captures conserved splice signals across phyla and reveals GC-rich introns specific to mammals and birds. We used this model to estimate the empirical splicing probability for every GT and AG in genomes, and modified minimap2 and miniprot to leverage pre-computed splicing probability during alignment. Evaluation on human long-read RNA-seq data and cross-species protein datasets showed our method greatly improves the junction accuracy especially for noisy long RNA-seq reads and proteins of distant homology. AVAILABILITY AND IMPLEMENTATION: https://github.com/lh3/minisplice.

Identifiers

PMID41484786
PMCPMC12766944

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Registered trials

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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.