conda create -n paramecium_align \
bowtie2 \
samtools \
fastqc \
multiqc \
subread \
r-base \
-c bioconda -c conda-forge -y
conda activate paramecium_align
chmod +x align_paramecium_single_end.sh
./align_paramecium_single_end.sh \
sample1.fastq.gz \
sample2.fastq.gz \
sample3.fastq.gz
or:
chmod +x align_paramecium_single_end.sh
./align_paramecium_single_end.sh *.fastq.gz
Output in the end will be:
paramecium_gene_counts.txt