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Rafsanjani Muhammod

dblp:250/1176 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2019
0000-0001-6415-172XORCID · reported

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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
feature selection
0.412019
PyFeat: a Python-based effective feature generation tool for DNA, RNA and protein sequences · Bioinform. 2019
Bioinformatics and computational biology › sequence analysis
sequence feature extraction
0.412019
PyFeat: a Python-based effective feature generation tool for DNA, RNA and protein sequences · Bioinform. 2019

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

adaboost · 0.4
YearPublicationVenuePosition
2019 PyFeat: a Python-based effective feature generation tool for DNA, RNA and protein sequences
abstract
MOTIVATION: Extracting useful feature set which contains significant discriminatory information is a critical step in effectively presenting sequence data to predict structural, functional, interaction and expression of proteins, DNAs and RNAs. Also, being able to filter features with significant information and avoid sparsity in the extracted features require the employment of efficient feature selection techniques. Here we present PyFeat as a practical and easy to use toolkit implemented in Python for extracting various features from proteins, DNAs and RNAs. To build PyFeat we mainly focused on extracting features that capture information about the interaction of neighboring residues to be able to provide more local information. We then employ AdaBoost technique to select features with maximum discriminatory information. In this way, we can significantly reduce the number of extracted features and enable PyFeat to represent the combination of effective features from large neighboring residues. As a result, PyFeat is able to extract features from 13 different techniques and represent context free combination of effective features. The source code for PyFeat standalone toolkit and employed benchmarks with a comprehensive user manual explaining its system and workflow in a step by step manner are publicly available. RESULTS: https://github.com/mrzResearchArena/PyFeat/blob/master/RESULTS.md. AVAILABILITY AND IMPLEMENTATION: Toolkit, source code and manual to use PyFeat: https://github.com/mrzResearchArena/PyFeat/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Rafsanjani Muhammod, Sajid Ahmed, Dewan Md. Farid 0001, Swakkhar Shatabda, Alok Sharma, Abdollah Dehzangi
Bioinform.1