Evidence map›Paper›PMID 25017736›Full record

ArticleBMC bioinformatics2014

Dataset size and composition impact the reliability of performance benchmarks for peptide-MHC binding predictions.

Yohan Kim, John Sidney, Søren Buus, Alessandro Sette, Morten Nielsen, Bjoern Peters

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Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

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42citing papers in PubMed
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3 · Its place in the literature

Who cites it

42 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Energy landscapes of peptide-MHC binding.PLoS computational biology · 2024
    Article
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  18. T Cell Epitope Predictions.Annual review of immunology · 2020
    Review
  19. Article
  20. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yohan Kim
John Sidney
Søren Buus
Alessandro Sette
Morten Nielsen
Bjoern PetersLa Jolla Institute for Allergy & Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA. bpeters@liai.org.

Funding

NIAID NIH HHS HHSN272201200010C
6 · The paper itself

Abstract

backgroundIt is important to accurately determine the performance of peptide:MHC binding predictions, as this enables users to compare and choose between different prediction methods and provides estimates of the expected error rate. Two common approaches to determine prediction performance are cross-validation, in which all available data are iteratively split into training and testing data, and the use of blind sets generated separately from the data used to construct the predictive method. In the present study, we have compared cross-validated prediction performances generated on our last benchmark dataset from 2009 with prediction performances generated on data subsequently added to the Immune Epitope Database (IEDB) which served as a blind set.

resultsWe found that cross-validated performances systematically overestimated performance on the blind set. This was found not to be due to the presence of similar peptides in the cross-validation dataset. Rather, we found that small size and low sequence/affinity diversity of either training or blind datasets were associated with large differences in cross-validated vs. blind prediction performances. We use these findings to derive quantitative rules of how large and diverse datasets need to be to provide generalizable performance estimates.

conclusionIt has long been known that cross-validated prediction performance estimates often overestimate performance on independently generated blind set data. We here identify and quantify the specific factors contributing to this effect for MHC-I binding predictions. An increasing number of peptides for which MHC binding affinities are measured experimentally have been selected based on binding predictions and thus are less diverse than historic datasets sampling the entire sequence and affinity space, making them more difficult benchmark data sets. This has to be taken into account when comparing performance metrics between different benchmarks, and when deriving error estimates for predictions based on benchmark performance.

Indexed as

AllelesAnimalsBenchmarkingComputational BiologyEpitopesHLA AntigensHumansMiceOligopeptidesProtein BindingReproducibility of ResultsEpitopesHLA AntigensMHC binding peptideOligopeptides

Identifiers

PMID25017736
PMCPMC4111843

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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.