Evidence map›Paper›PMID 33514769›Full record

ArticleScientific reports2021

Verifying explainability of a deep learning tissue classifier trained on RNA-seq data.

Melvyn Yap, Rebecca L Johnston, Helena Foley, Samual MacDonald, Olga Kondrashova, Khoa A Tran, Katia Nones, Lambros T Koufariotis, Cameron Bean, John V Pearson and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
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  7. Spatial Modularity of Innate Immune Networks Across Bactrian Camel Tissues.Animals : an open access journal from MDPI · 2025
    Article
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  9. Article
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  11. Article
  12. Article
  13. Review
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  18. Big Data in Gastroenterology Research.International journal of molecular sciences · 2023
    Review
  19. Article
  20. 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

12 authors.

Melvyn Yap *Max Kelsen, Brisbane, QLD, 4006, Australia.
Rebecca L Johnston *QIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.
Helena Foley *Max Kelsen, Brisbane, QLD, 4006, Australia.
Samual MacDonaldMax Kelsen, Brisbane, QLD, 4006, Australia.
Olga KondrashovaQIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.
Khoa A TranMax Kelsen, Brisbane, QLD, 4006, Australia.
Katia NonesQIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.
Lambros T KoufariotisQIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.
Cameron BeanMax Kelsen, Brisbane, QLD, 4006, Australia.
John V PearsonQIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.
Maciej TrzaskowskiMax Kelsen, Brisbane, QLD, 4006, Australia. maciej.trzaskowski@maxkelsen.com.
Nicola WaddellQIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia. nic.waddell@qimrberghofer.edu.au.

Funding

NCI NIH HHS
6 · The paper itself

Abstract

For complex machine learning (ML) algorithms to gain widespread acceptance in decision making, we must be able to identify the features driving the predictions. Explainability models allow transparency of ML algorithms, however their reliability within high-dimensional data is unclear. To test the reliability of the explainability model SHapley Additive exPlanations (SHAP), we developed a convolutional neural network to predict tissue classification from Genotype-Tissue Expression (GTEx) RNA-seq data representing 16,651 samples from 47 tissues. Our classifier achieved an average F1 score of 96.1% on held-out GTEx samples. Using SHAP values, we identified the 2423 most discriminatory genes, of which 98.6% were also identified by differential expression analysis across all tissues. The SHAP genes reflected expected biological processes involved in tissue differentiation and function. Moreover, SHAP genes clustered tissue types with superior performance when compared to all genes, genes detected by differential expression analysis, or random genes. We demonstrate the utility and reliability of SHAP to explain a deep learning model and highlight the strengths of applying ML to transcriptome data.

Indexed as

Deep LearningGenotypeRNA-SeqAlgorithmsHumansMachine LearningNeural Networks, ComputerOrgan Specificity

Identifiers

PMID33514769
PMCPMC7846764

What OpenQuestion holds

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LicenceCC BY
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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.