Evidence map›Paper›PMID 35639633›Full record

ArticleGigaScience2022

Profiling the baseline performance and limits of machine learning models for adaptive immune receptor repertoire classification.

Chakravarthi Kanduri, Milena Pavlović, Lonneke Scheffer, Keshav Motwani, Maria Chernigovskaya, 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  5. Forum on immune digital twins: a meeting report.NPJ systems biology and applications · 2024
    Review
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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

7 authors.

Chakravarthi KanduriCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo 0373, Norway.ORCID 0000-0002-4783-9060
Milena PavlovićCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo 0373, Norway.ORCID 0000-0002-2484-3868
Lonneke SchefferCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo 0373, Norway.ORCID 0000-0001-8900-075X
Keshav MotwaniDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida, FL 32610, USA.ORCID 0000-0003-1457-2731
Maria ChernigovskayaDepartment of Immunology and Oslo University Hospital, University of Oslo, Oslo, 0372, Norway.ORCID 0000-0002-1507-4171
Victor GreiffDepartment of Immunology and Oslo University Hospital, University of Oslo, Oslo, 0372, Norway.ORCID 0000-0003-2622-5032
Geir K SandveCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo 0373, Norway.ORCID 0000-0002-4959-1409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMachine learning (ML) methodology development for the classification of immune states in adaptive immune receptor repertoires (AIRRs) has seen a recent surge of interest. However, so far, there does not exist a systematic evaluation of scenarios where classical ML methods (such as penalized logistic regression) already perform adequately for AIRR classification. This hinders investigative reorientation to those scenarios where method development of more sophisticated ML approaches may be required.

resultsTo identify those scenarios where a baseline ML method is able to perform well for AIRR classification, we generated a collection of synthetic AIRR benchmark data sets encompassing a wide range of data set architecture-associated and immune state-associated sequence patterns (signal) complexity. We trained ≈1,700 ML models with varying assumptions regarding immune signal on ≈1,000 data sets with a total of ≈250,000 AIRRs containing ≈46 billion TCRβ CDR3 amino acid sequences, thereby surpassing the sample sizes of current state-of-the-art AIRR-ML setups by two orders of magnitude. We found that L1-penalized logistic regression achieved high prediction accuracy even when the immune signal occurs only in 1 out of 50,000 AIR sequences.

conclusionsWe provide a reference benchmark to guide new AIRR-ML classification methodology by (i) identifying those scenarios characterized by immune signal and data set complexity, where baseline methods already achieve high prediction accuracy, and (ii) facilitating realistic expectations of the performance of AIRR-ML models given training data set properties and assumptions. Our study serves as a template for defining specialized AIRR benchmark data sets for comprehensive benchmarking of AIRR-ML methods.

Indexed as

Machine LearningReceptors, ImmunologicReceptors, Immunologicadaptive immune receptor repertoiresAIRRbaseline performancebenchmarkingmachine learningML

Identifiers

PMID35639633
PMCPMC9154052

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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.