Evidence map›Paper›PMID 37217837›Full record

ArticleGenome biology and evolution2023

Unsupervised Deep Learning Can Identify Protein Functional Groups from Unaligned Sequences.

Kyle T David, Kenneth M Halanych

Abstract read
In one paragraph

Article in Genome biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Computational function prediction of bacteria and phage proteins.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  3. Article
  4. Article
  5. Article
4 · The record

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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.

Kyle T DavidDepartment of Biological Sciences, Auburn University, Auburn, AL, USA.ORCID 0000-0001-9907-789X
Kenneth M HalanychCenter for Marine Sciences, University of North Carolina Wilmington, NC, USA.ORCID 0000-0002-8658-9674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interpreting protein function from sequence data is a fundamental goal of bioinformatics. However, our current understanding of protein diversity is bottlenecked by the fact that most proteins have only been functionally validated in model organisms, limiting our understanding of how function varies with gene sequence diversity. Thus, accuracy of inferences in clades without model representatives is questionable. Unsupervised learning may help to ameliorate this bias by identifying highly complex patterns and structure from large datasets without external labels. Here we present DeepSeqProt, an unsupervised deep learning program for exploring large protein sequence datasets. DeepSeqProt is a clustering tool capable of distinguishing between broad classes of proteins while learning local and global structure of functional space. DeepSeqProt is capable of learning salient biological features from unaligned, unannotated sequences. DeepSeqProt is more likely to capture complete protein families and statistically significant shared ontologies within proteomes than other clustering methods. We hope this framework will prove of use to researchers and provide a preliminary step in further developing unsupervised deep learning in molecular biology.

Indexed as

BioinformaticsMachine LearningProtein Annotation

Identifiers

PMID37217837
PMCPMC10231473

What OpenQuestion holds

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LicenceCC BY-NC
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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.