Evidence map›Paper›PMID 42319798›Full record

ArticleGigaScience2026

ChatMDV: reducing technical barriers in bioinformatics analysis using large language models.

Maria Kiourlappou, Peter Todd, Yaxuan Kong, Jayesh Hire, Sibgathullah Furquan Nawab Mohammed, Devika Agarwal, Martin Sergeant, Stefan Zohren, Brian Marsden, Jim Hughes and 1 more

Abstract read
In one paragraph

Article in GigaScience, 2026. 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

11 authors.

Maria KiourlappouCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.ORCID 0000-0003-1792-9206
Peter ToddCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.ORCID 0009-0001-2137-930X
Yaxuan KongDepartment of Engineering Science, University of Oxford, Oxford, OX1 3PJ, UK.ORCID 0009-0006-8284-0055
Jayesh HireCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.
Sibgathullah Furquan Nawab MohammedCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.ORCID 0009-0008-8307-4211
Devika AgarwalKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Science, University of Oxford, Oxford, OX3 7FY, UK.ORCID 0000-0002-5203-307X
Martin SergeantWeatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, OX3 9DS, UK.ORCID 0000-0001-7264-2668
Stefan ZohrenDepartment of Engineering Science, University of Oxford, Oxford, OX1 3PJ, UK.ORCID 0000-0002-3392-0394
Brian MarsdenCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.ORCID 0000-0002-1937-4091
Jim HughesWeatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, OX3 9DS, UK.ORCID 0000-0002-8955-7256
Stephen TaylorCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7BN, UK.ORCID 0000-0002-3559-4334

Funding

University of Oxford
6 · The paper itself

Abstract

backgroundThe rapid advancement in single-cell, spatial omics, imaging, and genomic technologies requires robust analytical and visualisation platforms capable of managing complex biological data. Tools such as Multi-Dimensional Viewer (MDV) offer comprehensive interfaces for data exploration but often require advanced computational expertise and manual configuration to generate visualisation outputs, limiting accessibility for many users.

resultsWe present ChatMDV, a natural language interface integrated with MDV that enables users to generate high-quality, interactive visualisations and analyses through natural language commands. ChatMDV employs a retrieval-augmented generation pipeline in combination with large language models to translate user queries into executable, reproducible Python code and interactive output. This conversational layer facilitates both exploratory and targeted analyses in diverse biological domains. We demonstrate ChatMDV's capabilities using 3 datasets of increasing complexity: the Peripheral Blood Mononuclear Cells 3K single-cell RNA-sequencing (scRNA-seq) dataset, the lung cancer atlas scRNA-seq dataset included in the Human Cell Atlas, and the longitudinal TAURUS study scRNA-seq dataset. Across all use cases, ChatMDV produced high-quality, reproducible visualisations from simple natural language queries, achieving a high semantic success rate between 79% and 97% when visualising the datasets.

conclusionsBy bridging the gap between natural language processing and bioinformatics visualisation, ChatMDV reduces technical barriers, enhances reproducibility, and supports more inclusive scientific inquiry. Its modular design and adherence to Findability, Accessibility, Interoperability, and Reuse (FAIR) principles make it a scalable and adaptable framework for accelerating biological data analysis.

Indexed as

Computational BiologySoftwareHumansLarge Language ModelsNatural Language ProcessingSingle-Cell AnalysisUser-Computer Interfacebioinformaticsdata visualisationFAIR principleslarge language modelsnatural language interfaces

Identifiers

PMID42319798
PMCPMC13452166

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.