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Eran Barash

dblp:243/3563 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · none

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 · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics › microbial genomics
bacterial genome analysis
0.412019
BacPaCS - Bacterial Pathogenicity Classification via Sparse-SVM · Bioinform. 2019
Bioinformatics and computational biology
genomics
0.412019
BacPaCS - Bacterial Pathogenicity Classification via Sparse-SVM · Bioinform. 2019
Bioinformatics and computational biology
feature selection
0.112019
BacPaCS - Bacterial Pathogenicity Classification via Sparse-SVM · Bioinform. 2019
Bioinformatics and computational biology › genomics
machine learning for genomics
0.112019
BacPaCS - Bacterial Pathogenicity Classification via Sparse-SVM · Bioinform. 2019

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

sparse support vector machine · 0.4
YearPublicationVenuePosition
2019 BacPaCS - Bacterial Pathogenicity Classification via Sparse-SVM
abstract
MOTIVATION: Bacterial infections are a major cause of illness worldwide. However, most bacterial strains pose no threat to human health and may even be beneficial. Thus, developing powerful diagnostic bioinformatic tools that differentiate pathogenic from commensal bacteria are critical for effective treatment of bacterial infections. RESULTS: We propose a machine-learning approach for classifying human-hosted bacteria as pathogenic or non-pathogenic based on their genome-derived proteomes. Our approach is based on sparse Support Vector Machines (SVM), which autonomously selects a small set of genes that are related to bacterial pathogenicity. We implement our approach as a tool-'Bacterial Pathogenicity Classification via sparse-SVM' (BacPaCS)-which is fully automated and handles datasets significantly larger than those previously used. BacPaCS shows high accuracy in distinguishing pathogenic from non-pathogenic bacteria, in a clinically relevant dataset, comprising only human-hosted bacteria. Among the genes that received the highest positive weight in the resulting classifier, we found genes that are known to be related to bacterial pathogenicity, in addition to novel candidates, whose involvement in bacterial virulence was never reported. AVAILABILITY AND IMPLEMENTATION: The code and the resulting model are available at: https://github.com/barashe/bacpacs. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Eran Barash, Neta Sal-Man, Sivan Sabato, Michal Ziv-Ukelson
Bioinform.1