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I have been running into a problem in mapping when using genome_resquiggle,
And this is the error message: Alignment not produced. Potentially failed to locate BWA index files.
And all my fast5 was not mapped.
I had used graphmap to map, is it the same with bwa.
To check if it was my there was issues with my data and reference genome, I had extracted the sequences out using poretools and mapped with graphmap directly.
I was able to map at least 12% of my total reads.
Is there anything I can do to map at least 12% of my reads with genome_resquiggle?
So that I can use nanoraw to analyze my data?
The text was updated successfully, but these errors were encountered:
Hi,
I have been running into a problem in mapping when using genome_resquiggle,
And this is the error message: Alignment not produced. Potentially failed to locate BWA index files.
And all my fast5 was not mapped.
I had used graphmap to map, is it the same with bwa.
To check if it was my there was issues with my data and reference genome, I had extracted the sequences out using poretools and mapped with graphmap directly.
I was able to map at least 12% of my total reads.
Is there anything I can do to map at least 12% of my reads with genome_resquiggle?
So that I can use nanoraw to analyze my data?
The text was updated successfully, but these errors were encountered: