Small-RNA analysis
Runs with illumina small RNA-sequencing data. Aligns to the reference genome, gives QC metrics and finishes with gene count matrices.
smRNA-Seq is a bioinformatics best-practice analysis pipeline used for small RNA sequencing data analysis.
The pipeline uses Nextflow, a bioinformatics workflow tool. It pre-processes raw data from FastQ inputs, aligns the reads and performs extensive quality-control on the results.
nf-core/smrnaseq
https:
A small-RNA sequencing analysis pipeline - https://nf-co.re/smrnaseq
When we run analysis
We run this analysis for smRNA-seq projects where we have prepared the sequencing library in-house. If you have prepared a library yourself and we are just sequencing, please get in touch and mention that you would like us to run this analysis.
The analysis works with any of the species that have a reference genome available in AWS-iGenomes. If in doubt, please ask whether we can run the pipeline for you.
Input data
bcl2fastq demultiplexed FastQ files and a genome reference.
Results
The pipeline generates aligned BAM-files and gene count matrices, along with numerous quality control metrics. For more information, please see https://nf-co.re/smrnaseq/docs/output.
Last Updated: 14th July 2023