Evidence map›Paper›PMID 29940843›Full record

ArticleBMC bioinformatics2018

Semi-supervised machine learning for automated species identification by collagen peptide mass fingerprinting.

Muxin Gu, Michael Buckley

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
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  7. Article
  8. Paleoproteomics.Chemical reviews · 2022
    Review
  9. Article
  10. Review
  11. A primer for ZooMS applications in archaeology.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Review
  12. Article
  13. 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

2 authors.

Muxin GuMichael Smith Building, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PT, UK.
Michael BuckleyManchester Institute of Biotechnology, School of Earth and Environmental Sciences, The University of Manchester, 131 Princess Street, Manchester, M1 7DN, UK. m.buckley@manchester.ac.uk.ORCID 0000-0002-4166-8213

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiomolecular methods for species identification are increasingly being utilised in the study of changing environments, both at the microscopic and macroscopic levels. High-throughput peptide mass fingerprinting has been largely applied to bacterial identification, but increasingly used to identify archaeological and palaeontological skeletal material to yield information on past environments and human-animal interaction. However, as applications move away from predominantly domesticate and the more abundant wild fauna to a much wider range of less common taxa that do not yet have genetically-derived sequence information, robust methods of species identification and biomarker selection need to be determined.

resultsHere we developed a supervised machine learning algorithm for classifying the species of ancient remains based on collagen fingerprinting. The aim was to minimise requirements on prior knowledge of known species while yielding satisfactory sensitivity and specificity. The algorithm uses iterations of a modified random forest classifier with a similarity scoring system to expand its identified samples. We tested it on a set of 6805 spectra and found that a high level of accuracy can be achieved with a training set of five identified specimens per taxon.

conclusionsThis method consistently achieves higher accuracy than two-dimensional principal component analysis and similar accuracy with hierarchical clustering using optimised parameters, which greatly reduces requirements for human input. Within the vertebrata, we demonstrate that this method was able to achieve the taxonomic resolution of family or sub-family level whereas the genus- or species-level identification may require manual interpretation or further experiments. In addition, it also identifies additional species biomarkers than those previously published.

Indexed as

CollagenDNA FingerprintingHumansPeptidesSpecies SpecificitySupervised Machine LearningCollagenPeptidesAncient bone identificationCollagen fingerprintingHierarchical clusteringHigh-throughput species identificationPCASpecies biomarker identification

Identifiers

PMID29940843
PMCPMC6019507

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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.