hh.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Sequence homology score-based deep fuzzy network for identifying therapeutic peptides
University Of Electronic Science And Technology Of China, Chengdu, China; Wenzhou Medical University, Wenzhou, China; School Of Physical And Mathematical Sciences, Singapore City, Singapore.
University Of Nottingham Ningbo China, Ningbo, China.
School Of Physical And Mathematical Sciences, Singapore City, Singapore; Nanyang Technological University, Singapore City, Singapore.
University Of Electronic Science And Technology Of China, Chengdu, China; University Of Electronic Science And Technology Of China, Chengdu, China.ORCID iD: 0000-0001-6406-1142
Show others and affiliations
2024 (English)In: Neural Networks, ISSN 0893-6080, E-ISSN 1879-2782, Vol. 178, article id 106458Article in journal (Refereed) Published
Abstract [en]

The detection of therapeutic peptides is a topic of immense interest in the biomedical field. Conventional biochemical experiment-based detection techniques are tedious and time-consuming. Computational biology has become a useful tool for improving the detection efficiency of therapeutic peptides. Most computational methods do not consider the deviation caused by noise. To improve the generalization performance of therapeutic peptide prediction methods, this work presents a sequence homology score-based deep fuzzy echo-state network with maximizing mixture correntropy (SHS-DFESN-MMC) model. Our method is compared with the existing methods on eight types of therapeutic peptide datasets. The model parameters are determined by 10 fold cross-validation on their training sets and verified by independent test sets. Across the 8 datasets, the average area under the receiver operating characteristic curve (AUC) values of SHS-DFESN-MMC are the highest on both the training (0.926) and independent sets (0.923). © 2024 The Authors

Place, publisher, year, edition, pages
Kidlington: Elsevier, 2024. Vol. 178, article id 106458
Keywords [en]
Biological sequence classification, Membership function, Mixture correntropy, Therapeutic peptides
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:hh:diva-54276DOI: 10.1016/j.neunet.2024.106458ISI: 001259281900001PubMedID: 38901093Scopus ID: 2-s2.0-85196311865OAI: oai:DiVA.org:hh-54276DiVA, id: diva2:1883461
Available from: 2024-07-10 Created: 2024-07-10 Last updated: 2024-07-10Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Tiwari, Prayag

Search in DiVA

By author/editor
Zou, QuanTiwari, PrayagDing, Yijie
By organisation
School of Information Technology
In the same journal
Neural Networks
Biological Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 28 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf