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.