- Download zip and extract to root of your working directory OR Clone repo to your working diectory.
chomd +x bash_script.sh
- Copy/move all your fastq files to root of your working directory.
- If running stand alone, install the following together with their dependencies: fastqc, multiqc, flexbar(v3.x), hisat2 (v2.x.x), samtools, htseq and gnu-parallel. If running in HPC, make sure the modules are available.
- To generate raw transcript count tables, run bash_script.sh OR submit batch to SLURM.
Run standalone as
./bash_script.sh <link to reference genome> <link to anotation> <reference identifier>
If runnning in HPC, update the arguments in batch file andsbatch batch
. Compressed GZ file links are expected for reference genome and annotation. - Use R_script.rmd to do differential expression and enrichment analysis. All necssary packages are available in CRAN, Github, or Bioconductor and will be installed by the script if necessary.
Activity | Software |
---|---|
Alignment | HISAT2 |
Abundance | HTSeq |
Differential expression | DESeq2 |
Enrichement | Clusterprofiler |
Sharma A, Ference CM, Shantharaj D, Baldwin EA, Manthey JA, Jones JB. 2022. Transcriptomic analysis of changes in Citrus × microcarpa gene expression post Xanthomonas citri subsp. citri infection. European Journal of Plant Pathology 162:163–181. doi: http://dx.doi.org/10.1007/s10658-021-02394-6.