trying to run my dataset with trimmomatic
I have changed the files to fast-q-sanger, but it isn't recognising the format so I cant run as group set, and when I run as a single it fails with the fatal error exit code 1
please help
trying to run my dataset with trimmomatic
I have changed the files to fast-q-sanger, but it isn't recognising the format so I cant run as group set, and when I run as a single it fails with the fatal error exit code 1
please help
Hello,
The datatype is fastqsanger
. Make sure all inputs have this assigned. It is required for both single and paired-end data. At least one dataset has this assigned correctly. Test if the reads really are in fastqsanger
format with FastQC (Sanger Fastq +33, aka Illumina 1.8+), and based on those results, either use the FastqGrommer or directly assign the datatype fastqsanger
. This should resolve the problem.
Details covered in the Galaxy Support FAQs: https://galaxyproject.org/support/
Note: Starting with the latest Galaxy releases:
fastqsanger
format will have that datatype automatically assigned by the Upload tool when the datatype is "autodetected"..gz
), that you wish to remain uncompressed once the history, need to be assigned the datatype fastqsanger.gz
when loading through the Upload tool. fastqsanger
format, and loaded into the history with the fastqsanger
datatype assigned if the fastq reads are a match for that datatype specification.*Thanks! Jen, Galaxy team
admin edit: updated links and added notes about the Upload tool's datatype autodetection function.