Measuring Similarity among Protein Sequences Using a New Descriptor
The comparison of protein sequences according to similarity is a fundamental aspect of today’s biomedical research. With the developments of sequencing technologies, a large number of protein sequences increase exponentially in the public databases. Famous sequences’ comparison methods are alignment...
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Online Access: | http://dx.doi.org/10.1155/2019/2796971 |
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doaj-62188dfe9e814689a9f859fa494f341f2020-11-25T02:31:04ZengHindawi LimitedBioMed Research International2314-61332314-61412019-01-01201910.1155/2019/27969712796971Measuring Similarity among Protein Sequences Using a New DescriptorMervat M. Abo-Elkhier0Marwa A. Abd Elwahaab1Moheb I. Abo El Maaty2Department of Engineering Mathematics and Physics, Faculty of Engineering, Mansoura University, Mansoura 35516, EgyptDepartment of Engineering Mathematics and Physics, Faculty of Engineering, Mansoura University, Mansoura 35516, EgyptDepartment of Engineering Mathematics and Physics, Faculty of Engineering, Mansoura University, Mansoura 35516, EgyptThe comparison of protein sequences according to similarity is a fundamental aspect of today’s biomedical research. With the developments of sequencing technologies, a large number of protein sequences increase exponentially in the public databases. Famous sequences’ comparison methods are alignment based. They generally give excellent results when the sequences under study are closely related and they are time consuming. Herein, a new alignment-free method is introduced. Our technique depends on a new graphical representation and descriptor. The graphical representation of protein sequence is a simple way to visualize protein sequences. The descriptor compresses the primary sequence into a single vector composed of only two values. Our approach gives good results with both short and long sequences within a little computation time. It is applied on nine beta globin, nine ND5 (NADH dehydrogenase subunit 5), and 24 spike protein sequences. Correlation and significance analyses are also introduced to compare our similarity/dissimilarity results with others’ approaches, results, and sequence homology.http://dx.doi.org/10.1155/2019/2796971 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mervat M. Abo-Elkhier Marwa A. Abd Elwahaab Moheb I. Abo El Maaty |
spellingShingle |
Mervat M. Abo-Elkhier Marwa A. Abd Elwahaab Moheb I. Abo El Maaty Measuring Similarity among Protein Sequences Using a New Descriptor BioMed Research International |
author_facet |
Mervat M. Abo-Elkhier Marwa A. Abd Elwahaab Moheb I. Abo El Maaty |
author_sort |
Mervat M. Abo-Elkhier |
title |
Measuring Similarity among Protein Sequences Using a New Descriptor |
title_short |
Measuring Similarity among Protein Sequences Using a New Descriptor |
title_full |
Measuring Similarity among Protein Sequences Using a New Descriptor |
title_fullStr |
Measuring Similarity among Protein Sequences Using a New Descriptor |
title_full_unstemmed |
Measuring Similarity among Protein Sequences Using a New Descriptor |
title_sort |
measuring similarity among protein sequences using a new descriptor |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2019-01-01 |
description |
The comparison of protein sequences according to similarity is a fundamental aspect of today’s biomedical research. With the developments of sequencing technologies, a large number of protein sequences increase exponentially in the public databases. Famous sequences’ comparison methods are alignment based. They generally give excellent results when the sequences under study are closely related and they are time consuming. Herein, a new alignment-free method is introduced. Our technique depends on a new graphical representation and descriptor. The graphical representation of protein sequence is a simple way to visualize protein sequences. The descriptor compresses the primary sequence into a single vector composed of only two values. Our approach gives good results with both short and long sequences within a little computation time. It is applied on nine beta globin, nine ND5 (NADH dehydrogenase subunit 5), and 24 spike protein sequences. Correlation and significance analyses are also introduced to compare our similarity/dissimilarity results with others’ approaches, results, and sequence homology. |
url |
http://dx.doi.org/10.1155/2019/2796971 |
work_keys_str_mv |
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