This image facilitates the usage of Trimmomatic, a fastq trim and filter tool.
You should adapt and run the following command:
docker run --rm -v /your/data/dir:/data pegi3s/trimmomatic <SE or PE> <phred> /data/input.fastq /data/output.fastq
In this command, you should replace:
/your/data/dir to point to the directory that contains the FASTQ file you want to process.input.fastq to the actual name of your input file.<SE or PE> to SE in case of single-end sequencing and PE in case of paired-end sequencing.<phred> to either -phred33 or -phred64output.fastq to the actual name of your output fastq file.To see the trimmomatic usage, just run docker run --rm pegi3s/trimmomatic PE (or SE). To see the version, run docker run --rm pegi3s/trimmomatic -version.
Content type
Image
Digest
sha256:53bbea7fc…
Size
116.9 MB
Last updated
20 days ago
docker pull pegi3s/trimmomatic