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A cloud-based workflow to quantify transcript-expression levels in public cancer compendia.

P J Tatlow1, Stephen R Piccolo1,2

  • 1Department of Biology, Brigham Young University, Provo, Utah, USA.

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Summary
This summary is machine-generated.

Cloud computing enables researchers to analyze massive sequencing datasets without large data transfers. This study processed 12,307 RNA-Sequencing samples affordably, highlighting the need for preprocessing optimization.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Public sequencing data repositories are growing into petabytes, making local data transfer infeasible for researchers.
  • The National Cancer Institute is exploring cloud-computing environments for molecular data analysis to overcome data transfer limitations.
  • Cloud computing allows scientists to move analytical tools to the data and scale computational resources dynamically.

Purpose of the Study:

  • To evaluate the performance and cost-effectiveness of cloud-based configurations for processing large-scale RNA-Sequencing data.
  • To quantify transcript-expression levels for a substantial number of cancer cell line and genome atlas samples using cloud infrastructure.

Main Methods:

  • Quantified transcript-expression levels for 12,307 RNA-Sequencing samples from the Cancer Cell Line Encyclopedia and The Cancer Genome Atlas.
  • Utilized two distinct cloud-based configurations, employing preemptible virtual machines for cost-efficient processing.
  • Collected performance metrics during sample processing to track step durations and computational resource utilization.

Main Results:

  • Processed 12,307 RNA-Sequencing samples at a low cost of $0.09 per sample using preemptible virtual machines.
  • Detailed performance metrics were gathered, enabling tracking of processing step durations and computational resource usage.
  • While reference alignment and expression quantification are computationally efficient, preprocessing steps require further optimization.

Conclusions:

  • Cloud-based analysis of large sequencing datasets is feasible and cost-effective, enabling researchers to "bring tools to the data."
  • The study demonstrates a scalable and economical approach to analyzing transcript-expression levels from public compendia.
  • Optimization of preprocessing workflows remains crucial for maximizing efficiency in cloud-based genomic data analysis.