Uses MinVar and bamToFreq to convert next-generation sequencing reads (fastq/fastq.gz) to frequency files (csv).
This program is intended for use via Docker only. It can be used in the following way:
docker run -v <bamFolder>:/data/ mdoering88/fastqtofreq:latest /data/
or via an interactive session
docker run -v <bamFolder>:/data/ -it --entrypoint /bin/bash mdoering88/fastqtofreq:latest
and then calling run_minvar.sh
, minvar
, or bamToFreq
for custom processing.
- Only single-end sequencing reads are supported (use R1 file in case of paired-end data)
- The number of reads is downsampled to speed up the computations
- Only resistant-relevant regions of HIV-1 and HCV are supported