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Hi,
I got pod5 files and fastq file, and want to call methylation. I know Nanopolish does not support pod5 files, so I used blue-crab to convert pod5 files to blow5 files. Then I used slow5tools to convert the blow5 files to fast5 files. But I got errors:
[readdb] num reads: 5561098, num reads with path to fast5: 392000
fast5 files could not be located for 5169098 reads
[post-run summary] total reads: 375421, unparseable: 0, qc fail: 0, could not calibrate: 0, no alignment: 0, bad fast5: 5309727
Is there something wrong with my convert files?
The text was updated successfully, but these errors were encountered:
This is R10 or RNA004 data I believe? Nanopolish only supports R9 and that could be why. You may try f5c. The command line and output will be the same as nanopolish.
Hi,
I got pod5 files and fastq file, and want to call methylation. I know Nanopolish does not support pod5 files, so I used blue-crab to convert pod5 files to blow5 files. Then I used slow5tools to convert the blow5 files to fast5 files. But I got errors:
[readdb] num reads: 5561098, num reads with path to fast5: 392000
fast5 files could not be located for 5169098 reads
[post-run summary] total reads: 375421, unparseable: 0, qc fail: 0, could not calibrate: 0, no alignment: 0, bad fast5: 5309727
Is there something wrong with my convert files?
The text was updated successfully, but these errors were encountered: