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Firstly, I got the .paf with minimap2.
minimap2 -t 35 /data3/suisn/nanopore/bp/miniasm/miniasm.fasta /data3/suisn/nanopore/bp/filter/NanoFilt/nanofilt_trimmed.fastq > racon_round0.paf
Then, I used the folllowing command to run Racon
conda activate racon
racon -t 35 /data3/suisn/nanopore/bp/filter/NanoFilt/nanofilt_trimmed.fastq ./racon_round0.paf /data3/suisn/nanopore/bp/miniasm/miniasm.fasta > ./racon_round1.fasta &
I got the error message:
[racon::Polisher::initialize] loaded target sequences 16.907044 s
[racon::Polisher::initialize] loaded sequences 518.917979 s
terminate called after throwing an instance of 'std::invalid_argument'
what(): [bioparser::SamParser] error: invalid file format
Please give me some advises. Thank you.
The text was updated successfully, but these errors were encountered:
Did you by any chance used the wrong input? Errors in form of 'invalid file format' happen when the file extension (e.g. .paf/.sam) does not match the format of the file. Maybe you run minimap2 without option -a and saved it as .sam?
Hi, I have a problem with Racon.
Firstly, I got the .paf with minimap2.
minimap2 -t 35 /data3/suisn/nanopore/bp/miniasm/miniasm.fasta /data3/suisn/nanopore/bp/filter/NanoFilt/nanofilt_trimmed.fastq > racon_round0.paf
Then, I used the folllowing command to run Racon
conda activate racon
racon -t 35 /data3/suisn/nanopore/bp/filter/NanoFilt/nanofilt_trimmed.fastq ./racon_round0.paf /data3/suisn/nanopore/bp/miniasm/miniasm.fasta > ./racon_round1.fasta &
I got the error message:
[racon::Polisher::initialize] loaded target sequences 16.907044 s
[racon::Polisher::initialize] loaded sequences 518.917979 s
terminate called after throwing an instance of 'std::invalid_argument'
what(): [bioparser::SamParser] error: invalid file format
Please give me some advises. Thank you.
The text was updated successfully, but these errors were encountered: