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Hi,
First i would like to thank you for this awesome tool!
I recently started using fastq files with mixed uppercase and lowercase.
I'm using fqtools 2.3 2019-05-08 (zlib 1.2.8; htslib 1.8).
A test file I created named test_lowercase.fastq which contains:
I must say I first used an older version which I already had
fqtools 2.1 2016-10-04 (zlib 1.2.7; htslib 1.8) had the same results.
Decided to clone the repository again.
Am I using the command in the wrong way or is it a bug?
Thank you
The text was updated successfully, but these errors were encountered:
Using your test example (in a file "test.fastq", I find the command fqtools -dul count test.fastq works. The global options -dul (DNA bases; lowercase and uppercase) need to come before the command.
Hi,
First i would like to thank you for this awesome tool!
I recently started using fastq files with mixed uppercase and lowercase.
I'm using fqtools 2.3 2019-05-08 (zlib 1.2.8; htslib 1.8).
A test file I created named
test_lowercase.fastq
which contains:The command I'm using:
fqtools -l count test_lowercase.fastq
And the error is:
ERROR [line 2]: invalid sequence character (a)
I also tried:
fqtools -l -F count test_lowercase.fastq
Which outputs a different error:
I must say I first used an older version which I already had
fqtools 2.1 2016-10-04 (zlib 1.2.7; htslib 1.8) had the same results.
Decided to clone the repository again.
Am I using the command in the wrong way or is it a bug?
Thank you
The text was updated successfully, but these errors were encountered: