RMTA

RMTA automates read mapping and transcript assembly for RNA sequencing (RNA-seq) data to produce quality-filtered transcripts and read counts for downstream differential expression and transcriptome analyses.


Key Features:

  • Scalability and High-Throughput Processing: Handles thousands of RNA-seq datasets and supports both paired-end and single-end reads from FASTQ files as well as direct processing of SRA accessions.
  • Automated Quality Analysis and Filtering: Performs automated read quality analysis and applies filters for lowly expressed transcripts.
  • Differential Expression Analysis: Produces read counts required for differential expression analyses.
  • Containerization and Deployment: Distributed as a Docker container and deployable on cloud, local, and high-performance computing environments with integration into CyVerse's Discovery Environment for data management.
  • High-Throughput Parallelized Version (OSG-RMTA): Provides a parallelized implementation optimized for the Open Science Grid (OSG) to enable distributed high-throughput processing and job submission via the Discovery Environment.

Scientific Applications:

  • Transcriptomic Profiling: Captures comprehensive snapshots of gene expression from cells, tissues, or organisms using RNA-seq.
  • Comparative Genomics: Enables differential gene expression comparisons across biological conditions or species.
  • Functional Genomics: Supports investigation of functional elements and regulatory mechanisms through transcript-level analyses.

Methodology:

Performs read mapping and transcript assembly on FASTQ and SRA inputs, conducts automated read quality analysis, filters lowly expressed transcripts, and generates read counts; packaged in Docker with an OSG-parallelized option and integrated with CyVerse's Discovery Environment for data management and job submission.

Topics

Details

Programming Languages:
Shell
Added:
1/18/2021
Last Updated:
2/7/2021

Operations

Publications

Peri S, Roberts S, Kreko IR, McHan LB, Naron A, Ram A, Murphy RL, Lyons E, Gregory BD, Devisetty UK, Nelson ADL. Read Mapping and Transcript Assembly: A Scalable and High-Throughput Workflow for the Processing and Analysis of Ribonucleic Acid Sequencing Data. Frontiers in Genetics. 2020;10. doi:10.3389/fgene.2019.01361. PMID:32038716. PMCID:PMC6993073.

Peri S, Roberts S, Kreko IR, McHan LB, Naron A, Ram A, Murphy RL, Lyons E, Gregory BD, Devisetty UK, Nelson ADL. Read Mapping and Transcript Assembly: A Scalable and High-Throughput Workflow for the Processing and Analysis of Ribonucleic Acid Sequencing Data. Frontiers in Genetics. 2020;10. doi:10.3389/fgene.2019.01361. PMID:32038716. PMCID:PMC6993073.

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