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This repository has been archived by the owner on Jan 13, 2022. It is now read-only.
Hello,
It seems that something goes wrong with the 'prepare_mapped_reads.py' script but with no interruption.
Exactly, the inut reads of my fast5 and referefce_reads.fastq contains about 800k items,while over 780k reads was filtered out because they contain the N base in ref. sequence. The command logs are as below:
log:
Running prepare_mapping using flip-flop remapping
Converting references to labels using canonical alphabet ACGT and no modified bases
* 782465 reference seqeunces contain ambiguous bases not found in the provided alphabet and will be skipped.
* 44132 reads mapped successfully
* 1079868 reads failed to produce remapping results due to: No fasta reference found.
so, only 44132 reads successfully processed and saved to the mapped_reads.fast5 file.
How can i do with this?
Looking forward to your advice
Kerry, 20211127
The text was updated successfully, but these errors were encountered:
Hello,
It seems that something goes wrong with the 'prepare_mapped_reads.py' script but with no interruption.
Exactly, the inut reads of my fast5 and referefce_reads.fastq contains about 800k items,while over 780k reads was filtered out because they contain the N base in ref. sequence. The command logs are as below:
so, only 44132 reads successfully processed and saved to the mapped_reads.fast5 file.
How can i do with this?
Looking forward to your advice
Kerry, 20211127
The text was updated successfully, but these errors were encountered: