SortMeRNA

SortMeRNA identifies and removes ribosomal RNA (rRNA) sequences from next-generation sequencing (NGS) metatranscriptomic reads to enrich messenger RNA (mRNA) and other non-rRNA components for downstream analyses.


Key Features:

  • Rapid rRNA identification and removal: Rapidly identifies and removes rRNA sequences from large-scale NGS reads.
  • High-sensitivity rRNA matching: Matches rRNA fragments to its reference databases with high sensitivity.
  • Low computational running time: Maintains low computational running time suitable for extensive metatranscriptomic datasets.
  • rRNA fragment sorting: Separates and outputs rRNA-matching fragments to enrich mRNA and other non-rRNA components for downstream analysis.
  • Metatranscriptomic focus: Optimized for NGS data derived from microbial communities in metatranscriptomic studies.
  • Facilitates downstream analyses: Enables improved gene expression profiling and phylogenetic classification by reducing abundant rRNA reads.

Scientific Applications:

  • Metatranscriptomic preprocessing: Preprocessing of NGS metatranscriptomic data to remove rRNA for mRNA-focused analysis.
  • Gene expression analysis: Improves detection and quantification of mRNA for microbial gene expression studies.
  • Phylogenetic classification: Reduces rRNA-derived noise to support phylogenetic classification of species present in a sample.
  • Ecological and evolutionary studies: Supports ecological and evolutionary investigations by clarifying community transcriptomic signals.

Methodology:

Matches reads to rRNA reference databases to identify and remove rRNA fragments, achieving high-sensitivity detection while minimizing computational runtime.

Topics

Collections

Details

Tool Type:
command-line tool, web application
Operating Systems:
Linux, Mac
Programming Languages:
C++
Added:
1/17/2017
Last Updated:
11/24/2024

Operations

Publications

Kopylova E, Noé L, Touzet H. SortMeRNA: fast and accurate filtering of ribosomal RNAs in metatranscriptomic data. Bioinformatics. 2012;28(24):3211-3217. doi:10.1093/bioinformatics/bts611. PMID:23071270.

Documentation