Evidence map›Paper›PMID 37848619›Full record

ArticleGigaScience2022

simAIRR: simulation of adaptive immune repertoires with realistic receptor sequence sharing for benchmarking of immune state prediction methods.

Chakravarthi Kanduri, Lonneke Scheffer, Milena Pavlović, Knut Dagestad Rand, Maria Chernigovskaya, Oz Pirvandy, Gur Yaari, Victor Greiff, Geir K Sandve

Abstract read
In one paragraph

Article in GigaScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

9 authors.

Chakravarthi KanduriCentre for Bioinformatics, Department of Informatics, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0002-4783-9060
Lonneke SchefferCentre for Bioinformatics, Department of Informatics, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0001-8900-075X
Milena PavlovićCentre for Bioinformatics, Department of Informatics, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0002-2484-3868
Knut Dagestad RandCentre for Bioinformatics, Department of Informatics, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0003-3359-7619
Maria ChernigovskayaDepartment of Immunology and Oslo University Hospital, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0002-1507-4171
Oz PirvandyFaculty of Engineering, Bar-Ilan University, 5290002, Israel.ORCID 0000-0001-7213-2043
Gur YaariFaculty of Engineering, Bar-Ilan University, 5290002, Israel.ORCID 0000-0001-9311-9884
Victor GreiffDepartment of Immunology and Oslo University Hospital, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0003-2622-5032
Geir K SandveCentre for Bioinformatics, Department of Informatics, University of Oslo, 0373 Oslo, Norway.ORCID 0000-0002-4959-1409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMachine learning (ML) has gained significant attention for classifying immune states in adaptive immune receptor repertoires (AIRRs) to support the advancement of immunodiagnostics and therapeutics. Simulated data are crucial for the rigorous benchmarking of AIRR-ML methods. Existing approaches to generating synthetic benchmarking datasets result in the generation of naive repertoires missing the key feature of many shared receptor sequences (selected for common antigens) found in antigen-experienced repertoires.

resultsWe demonstrate that a common approach to generating simulated AIRR benchmark datasets can introduce biases, which may be exploited for undesired shortcut learning by certain ML methods. To mitigate undesirable access to true signals in simulated AIRR datasets, we devised a simulation strategy (simAIRR) that constructs antigen-experienced-like repertoires with a realistic overlap of receptor sequences. simAIRR can be used for constructing AIRR-level benchmarks based on a range of assumptions (or experimental data sources) for what constitutes receptor-level immune signals. This includes the possibility of making or not making any prior assumptions regarding the similarity or commonality of immune state-associated sequences that will be used as true signals. We demonstrate the real-world realism of our proposed simulation approach by showing that basic ML strategies perform similarly on simAIRR-generated and real-world experimental AIRR datasets.

conclusionsThis study sheds light on the potential shortcut learning opportunities for ML methods that can arise with the state-of-the-art way of simulating AIRR datasets. simAIRR is available as a Python package: https://github.com/KanduriC/simAIRR.

Indexed as

Computer Simulationadaptive immune receptor repertoiresAIRRbenchmarking of machine learning methodsMLshortcut learningsimulation of AIRR data

Identifiers

PMID37848619
PMCPMC10580376

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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.