I would need to obtain a conversion file from read idx used in MECAT and actual read name. I was looking at the function split_raw_dataset() and I found out that when printing read.header().data() and read.sequence().data() (single thread) the results do not have a correspondence in the input fastq file. They look like a mix of different reads (in bold the text that shouldn't be there) for both headers and sequences. Clear headers and sequences after each iteration seem not to affect the output. Am I missing something?
Hi,
I would need to obtain a conversion file from read idx used in MECAT and actual read name. I was looking at the function split_raw_dataset() and I found out that when printing read.header().data() and read.sequence().data() (single thread) the results do not have a correspondence in the input fastq file. They look like a mix of different reads (in bold the text that shouldn't be there) for both headers and sequences. Clear headers and sequences after each iteration seem not to affect the output. Am I missing something?
Priting headers:
Here's the code I'm referring to:
Thanks, Giulia