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SeqMule: Automated human exome/genome variants detection

https://doc-openbio.readthedocs.io/projects/seqmule/en/latest/

SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its configuration file.