tsRNAsearch

tsRNAsearch leverages Nextflow DSL2 to identify, quantify, and rank tRNA fragments (tRFs) and other non-coding RNAs from small RNA-sequencing datasets for comparative analysis and biomarker discovery.


Key Features:

  • Identification and quantification of ncRNAs: Detects and quantifies tRNA fragments (tRFs) and other non-coding RNAs in small RNA-seq data.
  • Nextflow DSL2 workflow: Implements processing and comparative analyses using Nextflow DSL2.
  • Handling sequence redundancy and short lengths: Addresses tRNA sequence redundancy and the short lengths of tRNAs/tRFs that complicate detection in sequencing data.
  • Comparative analysis across experimental groups: Compares control and treatment groups to detect ncRNAs with irregular read distribution profiles indicative of RNA cleavage events.
  • Innovative scoring system: Applies a combined score derived from four novel methods to rank tRNA fragments and other ncRNAs for differential abundance.

Scientific Applications:

  • Disease Biomarker Discovery: Applied to small RNA-seq datasets from chronic hepatitis-infected liver tissue and pancreatic ductal adenocarcinoma (PDAC), reproducing known tRFs and highlighting miR135b and other miRNA candidates as potential biomarkers.
  • Research in RNA Biology: Enables investigation of tRF biogenesis and functional roles by identifying cleavage-associated read distribution patterns and differentially abundant ncRNA species.

Methodology:

Implemented as a Nextflow DSL2 pipeline that performs a comparative differential expression analysis to search for tRNAs and other ncRNAs with irregular read distribution profiles indicative of cleavage events and uses a novel combined score from four methods to rank candidate ncRNAs.

Topics

Details

License:
MIT
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R, Shell, Python
Added:
11/15/2021
Last Updated:
11/15/2021

Operations

Publications

Donovan PD, McHale NM, Venø MT, Prehn JHM. tsRNAsearch: a pipeline for the identification of tRNA and ncRNA fragments from small RNA-sequencing data. Bioinformatics. 2021;37(23):4424-4430. doi:10.1093/bioinformatics/btab515. PMID:34255836.

PMID: 34255836
Funding: - JPND program: 17/JPND/3455 - SFI Research Centre for Chronic and Rare Neurological Diseases: 16/RC/3948

Links