I am trying to create fastq file(s) for each respective read group within the cram file. There should be a total of 4 different files instead of the 1 large fastq file that has been made. Are there any special parameters that need to be added if this is possible through cramtools?
I am trying to create fastq file(s) for each respective read group within the cram file. There should be a total of 4 different files instead of the 1 large fastq file that has been made. Are there any special parameters that need to be added if this is possible through cramtools?
java -jar cramtools-3.0.jar \ fastq \ -I cram_file.cram \ -R ref_genome \