Evidence map›Paper›PMID 39890780›Full record

ArticleNature communications2025

STICI: Split-Transformer with integrated convolutions for genotype imputation.

Mohammad Erfan Mowlaei, Chong Li, Oveis Jamialahmadi, Raquel Dias, Junjie Chen, Benyamin Jamialahmadi, Timothy Richard Rebbeck, Vincenzo Carnevale, Sudhir Kumar, Xinghua Shi

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. 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

10 authors.

Mohammad Erfan MowlaeiComputer & Information Sciences, College of Science and Technology, Temple University, Philadelphia, PA, USA.
Chong LiComputer & Information Sciences, College of Science and Technology, Temple University, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-1949-4074
Oveis JamialahmadiDepartment of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-7139-4738
Raquel DiasDepartment of Microbiology and Cell Science, University of Florida, Gainesville, FL, USA.
Junjie ChenSchool of Computer Science and Technology, Harbin Institute of Technology, Shenzhen, Guangdong, China.
Benyamin JamialahmadiDavid R. Cheriton School of Computer Science, University of Waterloo, Waterloo, ON, Canada.
Timothy Richard RebbeckDivision of Population Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4799-1900
Vincenzo CarnevaleInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-1918-8280
Sudhir KumarComputer & Information Sciences, College of Science and Technology, Temple University, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-9918-8212
Xinghua ShiComputer & Information Sciences, College of Science and Technology, Temple University, Philadelphia, PA, USA. mindyshi@temple.edu.ORCID http://orcid.org/0000-0003-4662-3177

Funding

Identifying and Characterizing the Full Spectrum of Haplotype-resolved Structural Variation in Human GenomesU24HG007497 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Evan Eichler, Jan Oliver Korbel · 2019 to 2026
$17.2M
Regulation of the Intestinal Ca2+ Channels TRPV6R01GM093290 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI CARNEVALE, VINCENZO, ROHACS, TIBOR · 2011 to 2025
$4.9M
Methods For Evolutionary Genomics AnalysisR35GM139540 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI Sudhir Kumar · 2021 to 2026
$2.9M
Inferring molecular evolutionary rates and divergence datesR01GM126567 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI KUMAR, SUDHIR · 2018 to 2020
$951k
NHGRI NIH HHS U24 HG007497NIGMS NIH HHS R01 GM093290NIGMS NIH HHS R01 GM126567NIGMS NIH HHS R35 GM139540
6 · The paper itself

Abstract

Despite advances in sequencing technologies, genome-scale datasets often contain missing bases and genomic segments, hindering downstream analyses. Genotype imputation addresses this issue and has been a cornerstone pre-processing step in genetic and genomic studies. Although various methods have been widely adopted for genotype imputation, it remains challenging to impute certain genomic regions and large structural variants. Here, we present a transformer-based framework, named STICI, for accurate genotype imputation. STICI models automatically learn genome-wide patterns of linkage disequilibrium, evidenced by much higher imputation accuracy in regions with highly linked variants. Our imputation results on the human 1000 Genomes Project and non-human genomes show that STICI can achieve high imputation accuracy comparable to the state-of-the-art genotype imputation methods, with the additional capability to impute multi-allelic variants and various types of genetic variants. STICI can be trained for any collection of genomes automatically using self-supervision. Moreover, STICI shows excellent performance without needing any special presuppositions about the underlying patterns in collections of non-human genomes, pointing to adaptability and applications of STICI to impute missing genotypes in any species.

Indexed as

GenomicsGenotypeAlgorithmsGenome, HumanGenome-Wide Association StudyHumansLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotideSoftware

Identifiers

PMID39890780
PMCPMC11785734

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.