Melola Discovery

← Melola Discovery

Open access Jurnal SINTA 1

Towards enhancing the user experience of ChIP-Seq data analysis web tools

International Journal of Electrical and Computer Engineering (IJECE) · Vol. 12 No. 5 (2022)

DOI
10.11591/ijece.v12i5.pp5236-5247
ISSN
2722-2578, 2088-8708
Published
2022-10-01
Publisher
Institute of Advanced Engineering and Science
License
creativecommons.org/licenses/by-sa/4.0

Abstract

Deoxyribonucleic acid (DNA) sequencing is the process of locating the sequence of the main chemical bases in the DNA. Next-generation sequencing (NGS) is the state-of-the-art DNA sequencing technique. The NGS technique advanced the biological science in analyzing human DNA due to its scalability, high throughput, and speed. Analyzing human DNA is crucial to determine the ability of a person to develop certain diseases and his ability to respond to certain medications. ChIP-sequencing is a method that combines chromatin immunoprecipitation (ChIP) with NGS sequencing to analyze protein interactions with DNA to identify binding sites. Many online web tools have been developed to conduct ChIP-Seq data analysis to either discover or find motifs, i.e., patterns of binding sites. Since these ChIP-Seq web tools need to be used by clinical practitioners, they must comply to the web-related usability tasks including effectiveness, efficiency and satisfaction to enhance the user experience (UX). To that end, we have conducted an empirical study to understand their UX design. Specifically, we have evaluated the usability of 8 widely used ChIP-Seq web tools against 6 known usability quality metrics. Our study shows that the design of the studied ChIP-Seq web tools does not follow the UX design principles.

Collaboration network of the authors

11 authors · 27 co-authorship links · 8 across different organisations

Hover or tap a name to highlight its co-authors. Double-click to open the author's page.

  • Jordan University of Science and Technology
  • Yarmouk University
  • Al-Zaytoonah University of Jordan
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
  • Thicker line = more joint articles · bigger circle = more articles
Show as table
Co-authorOrganisationJoint articles
Sa’ad A. Al-ZboonJordan University of Science and Technology9
Saja Khaled TawalbehJordan University of Science and Technology3
Asma’a Al-MnayyisYarmouk University2
Sanaa Abu AlasalJordan University of Science and Technology2
Mohammad A. AlsmiratJordan University of Science and Technology2
Shadi Mahmoud Faleh AlZu’biAl-Zaytoonah University of Jordan1
Mahmoud Al‐AyyoubJordan University of Science and Technology1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

This record comes from Crossref (what the publisher deposited), because the journal's own OAI-PMH endpoint could not be harvested.

Metadata source: Crossref API (cadangan, berdasarkan ISSN) https://api.crossref.org/journals/2088-8708/works, first harvested 27 Okt 2026, last seen 27 Okt 2026.
Metadata as oai_dc, converted from Crossref
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/"><dc:title>Towards enhancing the user experience of ChIP-Seq data analysis web tools</dc:title><dc:creator>Hammad, Mahmoud</dc:creator><dc:creator>Baker, Qanita Bani</dc:creator><dc:creator>Al-Smadi, Mohammed</dc:creator><dc:creator>Alrashdan, Wesam</dc:creator><dc:description>&lt;jats:p&gt;&amp;lt;p&amp;gt;Deoxyribonucleic acid (DNA) sequencing is the process of locating the sequence of the main chemical bases in the DNA. Next-generation sequencing (NGS) is the state-of-the-art DNA sequencing technique. The NGS technique advanced the biological science in analyzing human DNA due to its scalability, high throughput, and speed. Analyzing human DNA is crucial to determine the ability of a person to develop certain diseases and his ability to respond to certain medications. ChIP-sequencing is a method that combines chromatin immunoprecipitation (ChIP) with NGS sequencing to analyze protein interactions with DNA to identify binding sites. Many online web tools have been developed to conduct ChIP-Seq data analysis to either discover or find motifs, i.e., patterns of binding sites. Since these ChIP-Seq web tools need to be used by clinical practitioners, they must comply to the web-related usability tasks including effectiveness, efficiency and satisfaction to enhance the user experience (UX). To that end, we have conducted an empirical study to understand their UX design. Specifically, we have evaluated the usability of 8 widely used ChIP-Seq web tools against 6 known usability quality metrics. Our study shows that the design of the studied ChIP-Seq web tools does not follow the UX design principles.&amp;lt;/p&amp;gt;&lt;/jats:p&gt;</dc:description><dc:publisher>Institute of Advanced Engineering and Science</dc:publisher><dc:date>2022-10-01</dc:date><dc:type>info:eu-repo/semantics/article</dc:type><dc:format>application/pdf</dc:format><dc:identifier>https://doi.org/10.11591/ijece.v12i5.pp5236-5247</dc:identifier><dc:identifier>10.11591/ijece.v12i5.pp5236-5247</dc:identifier><dc:source>International Journal of Electrical and Computer Engineering (IJECE); Vol 12 No 5 (2022); 5236</dc:source><dc:source>2722-2578</dc:source><dc:source>2088-8708</dc:source><dc:relation>https://ijece.iaescore.com/index.php/IJECE/article/viewFile/27159/15951</dc:relation><dc:rights>http://creativecommons.org/licenses/by-sa/4.0</dc:rights></oai_dc:dc>