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BiSpark: a Spark-based highly scalable aligner for bisulfite sequencing data.


ABSTRACT: BACKGROUND:Bisulfite sequencing is one of the major high-resolution DNA methylation measurement method. Due to the selective nucleotide conversion on unmethylated cytosines after treatment with sodium bisulfite, processing bisulfite-treated sequencing reads requires additional steps which need high computational demands. However, a dearth of efficient aligner that is designed for bisulfite-treated sequencing becomes a bottleneck of large-scale DNA methylome analyses. RESULTS:In this study, we present a highly scalable, efficient, and load-balanced bisulfite aligner, BiSpark, which is designed for processing large volumes of bisulfite sequencing data. We implemented the BiSpark algorithm over the Apache Spark, a memory optimized distributed data processing framework, to achieve the maximum data parallel efficiency. The BiSpark algorithm is designed to support redistribution of imbalanced data to minimize delays on large-scale distributed environment. CONCLUSIONS:Experimental results on methylome datasets show that BiSpark significantly outperforms other state-of-the-art bisulfite sequencing aligners in terms of alignment speed and scalability with respect to dataset size and a number of computing nodes while providing highly consistent and comparable mapping results. AVAILABILITY:The implementation of BiSpark software package and source code is available at https://github.com/bhi-kimlab/BiSpark/ .

SUBMITTER: Soe S 

PROVIDER: S-EPMC6288881 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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BiSpark: a Spark-based highly scalable aligner for bisulfite sequencing data.

Soe Seokjun S   Park Yoonjae Y   Chae Heejoon H  

BMC bioinformatics 20181210 1


<h4>Background</h4>Bisulfite sequencing is one of the major high-resolution DNA methylation measurement method. Due to the selective nucleotide conversion on unmethylated cytosines after treatment with sodium bisulfite, processing bisulfite-treated sequencing reads requires additional steps which need high computational demands. However, a dearth of efficient aligner that is designed for bisulfite-treated sequencing becomes a bottleneck of large-scale DNA methylome analyses.<h4>Results</h4>In th  ...[more]

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