Abstract
Next Generation Sequencing (NGS) technologies produce massive amount of low cost data that is very much useful in genomic study and research. However, data produced by NGS is affected by different errors such as substitutions, deletions or insertion. It is essential to differentiate between true biological variants and alterations occurred due to errors for accurate downstream analysis. Many types of methods and tools have been developed for NGS error correction. Some of these methods only correct substitutions errors whereas others correct multi types of data errors. In this article, a comprehensive evaluation of three types of methods (k-spectrum based, Multi- sequencing alignment and Hybrid based) is presented which are implemented and adopted by different tools. Experiments have been conducted to compare the performance based on runtime and error correction rate. Two different computing platforms have been used for the experiments to evaluate effectiveness of runtime and error correction rate. The mission and aim of this comparative evaluation is to provide recommendations for selection of suitable tools to cope with the specific needs of users and practitioners. It has been noticed that k-mer spectrum based methodology generated superior results as compared to other methods. Amongst all the tools being utilized, Racer has shown eminent performance in terms of error correction rate and execution time for both small as well as large data sets. In multisequence alignment based tools, Karect depicts excellent error correction rate whereas Coral shows better execution time for all data sets. In hybrid based tools, Jabba shows better error correction rate and execution time as compared to brownie. Computing platforms mostly affect execution time but have no general effect on error correction rate.
Highlights
Gigantic amount of data is originated with the help of generation sequencing technologies at lowest cost and high throughput
Next Generation Sequencing (NGS) demands high-power CPU and various algorithms that can work in parallel mode for bioinformatics studies
Most of the tools and methods focus on removing the substitution errors [3]
Summary
Gigantic amount of data is originated with the help of generation sequencing technologies at lowest cost and high throughput. As compared to old generation of sequencing data (the first-generation technology) for example Sanger NGS data faces high challenges of error rate. NGS demands high-power CPU and various algorithms that can work in parallel mode for bioinformatics studies. It needs the spacious memory and execution time for total data that may cause issues for data management. NGS technologies produce different tools such as Illumina and Solid to induce the substitution error, whereas the Roche 454 and Ion torrent create the insertion and deletion error. It is key step to remove the data error before any analysis can be made These errors disturb the accuracy of algorithm it is beneficial to rectify data before analysis to conclude better results in downstream analysis [4]
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: International Journal of Advanced Computer Science and Applications
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.