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Biology subjects

Ogasawara, O.

Publications and source records attributed to Ogasawara, O..

2 recordsLinked to original sources

Accumulating computational resource usage of genomic data analysis workflow to optimize cloud computing instance selection

BackgroundContainer virtualization technologies such as Docker became popular in the bioinformatics domain as they improve portability and reproducibility of software deployment. Along with software packaged in containers, the workflow description standards Common Workflow Language also enabled to perform data analysis on multiple different computing environments with ease. These technologies accelerate the use of on-demand cloud computing platform which can scale out according to the amount of data. However, to optimize the time and the budget on a use of cloud, users need to select a suitable instance type corresponding to the resource requirements of their workflows.\n\nResultsWe developed CWL-metrics, a system to collect runtime metrics of Docker containers and workflow metadata to analyze resource requirement of workflows. We demonstrated the analysis by using seven transcriptome quantification workflows on six instance types. The result showed instance type options of lower financial cost and faster execution time with required amount of computational resources.\n\nConclusionsThe summary of resource requirements of workflow executions provided by CWL-metrics can help users to optimize the selection of cloud computing instance. The runtime metrics data also accelerate to share workflows among different workflow management frameworks.

bioinformatics↗

Integrative analysis of transcription factor occupancy at enhancers and disease risk loci in noncoding genomic regions

Noncoding regions of the human genome possess enhancer activity and harbor risk loci for heritable diseases. Whereas the binding profiles of multiple transcription factors (TFs) have been investigated, integrative analysis with the large body of public data available so as to provide an overview of the function of such noncoding regions has remained a challenge. Here we have fully integrated public ChIP-seq and DNase-seq data (n ~ 70,000), including those for 743 human transcription factors (TFs) with 97 million binding sites, and have devised a data- mining platform --designated ChIP-Atlas--to identify significant TF-genome, TF-gene, and TF-TF interactions. Using this platform, we found that TFs enriched at macrophage or T-cell enhancers also accumulated around risk loci for autoimmune diseases, whereas those enriched at hepatocyte or macrophage enhancers were preferentially detected at loci associated with HDL-cholesterol levels. Of note, we identified \"hotspots\" around such risk loci that accumulated multiple TFs and are therefore candidates for causal variants. Integrative analysis of public chromatin-profiling data is thus able to identify TFs and tissues associated with heritable disorders.

genomics↗