Abstract

BackgroundClustering is a key step in the processing of Expressed Sequence Tags (ESTs). The primary goal of clustering is to put ESTs from the same transcript of a single gene into a unique cluster. Recent EST clustering algorithms mostly adopt the alignment-free distance measures, where they tend to yield acceptable clustering accuracies with reasonable computational time. Despite the fact that these clustering methods work satisfactorily on a majority of the EST datasets, they have a common weakness. They are prone to deliver unsatisfactory clustering results when dealing with ESTs from the genes derived from the same family. The root cause is the distance measures applied on them are not sensitive enough to separate these closely related genes.Methodology/Principal FindingsWe propose a hybrid distance measure that combines the global and local features extracted from ESTs, with the aim to address the clustering problem faced by ESTs derived from the same gene family. The clustering process is implemented using the DBSCAN algorithm. We test the hybrid distance measure on the ten EST datasets, and the clustering results are compared with the two alignment-free EST clustering tools, i.e. wcd and PEACE. The clustering results indicate that the proposed hybrid distance measure performs relatively better (in terms of clustering accuracy) than both EST clustering tools.Conclusions/SignificanceThe clustering results provide support for the effectiveness of the proposed hybrid distance measure in solving the clustering problem for ESTs that originate from the same gene family. The improvement of clustering accuracies on the experimental datasets has supported the claim that the sensitivity of the hybrid distance measure is sufficient to solve the clustering problem.

Highlights

  • Sequencing techniques have progressed rapidly in recent years, various types of sequence data have been produced and they are publicly available for research purpose

  • The correctness of our clustering result is evaluated based on the Expressed Sequence Tags (ESTs) libraries from the genome browser, where the libraries are constructed based on the alignment of ESTs on the human genome assembly [45]

  • The same datasets are tested with two alignment-free EST clustering tools and their clustering results are compared and discussed

Read more

Summary

Introduction

Sequencing techniques have progressed rapidly in recent years, various types of sequence data have been produced and they are publicly available for research purpose. Despite many genome assemblies are available at present, research on expressed sequence tag (EST) is still on-going, due to it is a cost-effective resource for expression data analysis [1], [2], functional analysis [3], and single-nucleotide polymorphisms [4]. One of the key steps in the EST processing pipeline is clustering. Clustering is a key step in the processing of Expressed Sequence Tags (ESTs). Despite the fact that these clustering methods work satisfactorily on a majority of the EST datasets, they have a common weakness. They are prone to deliver unsatisfactory clustering results when dealing with ESTs from the genes derived from the same family. The root cause is the distance measures applied on them are not sensitive enough to separate these closely related genes

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.