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Md-Nafiz Hamid

dblp:230/8367 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 75% Computational social science and digital humanities · 25%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein function prediction
antimicrobial peptide prediction
0.412019
Identifying antimicrobial peptides using word embedding with deep recurrent neural networks · Bioinform. 2019
Bioinformatics and computational biology › proteomics › peptide analysis
peptide classification
0.412019
Identifying antimicrobial peptides using word embedding with deep recurrent neural networks · Bioinform. 2019
Bioinformatics and computational biology › protein sequence analysis
protein sequence representation
0.412019
Identifying antimicrobial peptides using word embedding with deep recurrent neural networks · Bioinform. 2019
Computational social science and digital humanities › computational linguistics
word embedding
0.412019
Identifying antimicrobial peptides using word embedding with deep recurrent neural networks · Bioinform. 2019

Methods — techniques the papers use, named apart from their topics

word embeddings · 0.4recurrent neural network · 0.4
YearPublicationVenuePosition
2019 Identifying antimicrobial peptides using word embedding with deep recurrent neural networks
abstract
MOTIVATION: Antibiotic resistance constitutes a major public health crisis, and finding new sources of antimicrobial drugs is crucial to solving it. Bacteriocins, which are bacterially produced antimicrobial peptide products, are candidates for broadening the available choices of antimicrobials. However, the discovery of new bacteriocins by genomic mining is hampered by their sequences' low complexity and high variance, which frustrates sequence similarity-based searches. RESULTS: Here we use word embeddings of protein sequences to represent bacteriocins, and apply a word embedding method that accounts for amino acid order in protein sequences, to predict novel bacteriocins from protein sequences without using sequence similarity. Our method predicts, with a high probability, six yet unknown putative bacteriocins in Lactobacillus. Generalized, the representation of sequences with word embeddings preserving sequence order information can be applied to peptide and protein classification problems for which sequence similarity cannot be used. AVAILABILITY AND IMPLEMENTATION: Data and source code for this project are freely available at: https://github.com/nafizh/NeuBI. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Md-Nafiz Hamid, Iddo Friedberg
Bioinform.1