Evidence map›Paper›PMID 41283814›Full record

ArticleBriefings in bioinformatics2025

Introducing a foundational sequence transformer for range adaptive nucleotide decoding (STRAND).

Shant Ayanian, Collin Osborne, Clark Xu, Carl Molnar, Pravat Das, Xoab Perez, Natalia Vassilieva, Vinay Pondenkandath, Bhargav Kanakiya, Ganesh Venkatesh and 9 more

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Shant AyanianMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.ORCID 0000-0001-9319-9001
Collin OsborneMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Clark XuMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Carl MolnarMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Pravat DasMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Xoab PerezMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Natalia VassilievaCerebras Systems, Inc., 1237 E. Arques Ave, Sunnyvale 94085, CA, United States.
Vinay PondenkandathCerebras Systems, Inc., 1237 E. Arques Ave, Sunnyvale 94085, CA, United States.
Bhargav KanakiyaCerebras Systems, Inc., 1237 E. Arques Ave, Sunnyvale 94085, CA, United States.
Ganesh VenkateshCerebras Systems, Inc., 1237 E. Arques Ave, Sunnyvale 94085, CA, United States.
May LevinCerebras Systems, Inc., 1237 E. Arques Ave, Sunnyvale 94085, CA, United States.
Matt RedlonMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Marc BlasiMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Vijay H ShahMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Matthew CallstromMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Konstantinos N LazaridisMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Panos KorfiatisMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.
Alexander RyuMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.ORCID 0000-0002-0138-5112
Elena MyasoedovaMayo Clinic, 200 1st St SW, Rochester 55905, MN, United States.ORCID 0000-0003-2006-1436

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of high-throughput sequencing has led to an exponential increase in genomic data, highlighting the need for efficient and accurate models to analyze and interpret this information. In this study, we introduce a novel, exomic foundational model that leverages a combination of the human reference genome and multispecies data to improve variant detection and interpretation. Our model utilizes a short-range transformer architecture and is trained on a large dataset of human exomic sequences derived from the Tapestry study. Through a series of ablation studies and scaling experiments, we demonstrate the effectiveness of our model in predicting next token accuracy and identifying clinically pathogenic variants. We also show that our model outperforms existing models in a range of downstream tasks, including variant effect prediction and disease state identification. In fact, our largest sequence transformer for range adaptive nucleotide decoding variant (1B parameters) surpassed previous benchmarks, demonstrating a mean accuracy of 0.880 [an 8.2% improvement over the original nucleotide transformer (NT) and a 7% improvement over NT-v2]. Furthermore, we construct a unique exomic ClinVar dataset to evaluate the model's performance on pathogenicity and disease states. Our results highlight the potential of this model to improve our understanding of the human exome and its role in disease. The model and its applications have significant implications for genomics-based diagnosis and personalized medicine, including tailored therapeutic development.

Indexed as

Genome, HumanGenomicsHigh-Throughput Nucleotide SequencingNucleotidesSequence Analysis, DNAAlgorithmsComputational BiologyHumansNucleotidesbenchmarkingexomemachine learningrheumatoid arthritistransformer architecture

Identifiers

PMID41283814
PMCPMC12641612

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LicenceCC BY
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.