ZHU TAO

You should download `tests/test.bam` from this github directory and put it in your current folder

In addition, I tried to use `--fastq_chars` and it gave the following results ``` Reading FASTQ file 100% Read 54687 sequences. Qmin 42, QMax 109, Range 68 Guess: -fastq_qmin 9...

@torognes I agree with issuing a warning instead of a fatal error. Fatal error is too nervous

Sorry for my late response, but I don't know why the email notification in github doesn't work. It should be work in python 3.8, but not in 3.9. I've updated...

I'm so sorry for my late reply. What's your python's version?

Thanks. Please try to debug as this: (1) in your console, type `samtools --version` to see the results (2) In your console, type `python3` to enter the python3 console, then...

Hello, can you show me what's your input and parameters? (If the file is big, give a part of sequence is OK)

I download the template fasta (in fact it is CDS, not genome) and run command like this (input is your iD: Cm000010.1): ``` primertool full input RL.v1.0.CDS.fa --type SEQUENCE_INCLUDED_REGION -a...

Please be note that genome has to be indexed by samtools first, and make sure the index file is correct

How about running in the command line?