nf-core/smartseq2
A pipeline for processing single cell RNA-seq data generated with the SmartSeq2 protocol.
22.10.6
.
Learn more.
Output
This document describes the output produced by the pipeline. Most of the plots are taken from the MultiQC report, which summarises results at the end of the pipeline.
Table of contents
FastQC
FastQC gives general quality metrics about your reads. It provides information about the quality score distribution across your reads, the per base sequence content (%T/A/G/C). You get information about adapter contamination and other overrepresented sequences.
For further reading and documentation see the FastQC help.
NB: The FastQC plots displayed in the MultiQC report shows untrimmed reads. They may contain adapter sequence and potentially regions with low quality. To see how your reads look after trimming, look at the FastQC reports in the
trim_galore
directory.
Output directory: results/fastqc
sample_fastqc.html
- FastQC report, containing quality metrics for your untrimmed raw fastq files
zips/sample_fastqc.zip
- zip file containing the FastQC report, tab-delimited data file and plot images
MultiQC
MultiQC is a visualisation tool that generates a single HTML report summarising all samples in your project. Most of the pipeline QC results are visualised in the report and further statistics are available in within the report data directory.
The pipeline has special steps which allow the software versions used to be reported in the MultiQC output for future traceability.
Output directory: results/multiqc
multiqc_report.html
- MultiQC report - a standalone HTML file that can be viewed in your web browser
multiqc_data/
- Directory containing parsed statistics from the different tools used in the pipeline
For more information about how to use MultiQC reports, see http://multiqc.info
BraCeR
BraCeR is a tool for reconstruction of B cell receptor sequences from single-cell RNA-seq data.
Output direcetory: results/BraCeR
filtered_BCR_summary/IMGT_gapped_db.tab
- summary of all detected Immunoglobuling chains for all cells
[CELL]
- For each cell, there’s a dedicated output directory containing more detailed information than what’s in the summary.
TraCeR
TraCeR is a tool for reconstruction of T cell receptor sequences from single-cell RNA-seq data.
Output directory: results/TraCeR
filtered_TCR_summary/cell_data.csv
- summary of all detected T cell receptor chains for all cells
[CELL]
- For each cell, there’s a dedicated output directory containing more detailed information than what’s in the summary.
STAR
STAR is a ultra-fast RNA-seq aligner.
Output directory: results/STAR
[CELL]/[CELL].Aligned.toTranscriptome.out.bam
- BAM file aligned to the transcriptome
[CELL]/[CELL].Aligned.sortedByCoord.out.bam
- The same BAM file, but sorted
[CELL]/[CELL].Log.final.out
- The STAR alignment report, containing mapping results summary.
RSEM
RSEM is a tool for the accurate quantification of gene and isoform expression from RNA-seq data. We use it to compute Transcript per Million (TPM)-normalized gene expression values for each cell.
Output directory: results/RSEM
resultTPM.txt
- tab separated TPM matrix for all genes and cells.
[CELL]
- For each cell, there’s a dedicated output directory, containing the raw results and statistics.
featureCounts
featureCounts is a highly-efficent tool that summarizes mapped reads for genomic features. We use it to compute raw count values for each gene and cell.
Output directory: results/featureCounts
resultCOUNT.txt
- tab sparated count matrix for all genes and cells.
[CELL]
- For each cell, there’s a dedicated output directory, containing the raw results and statistics.