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CHECKPOINT: Unitig assembly completed.
CMD: bash -euo pipefail -c 'abyss-pe graph=adj --directory=/home/orp/Oyster_River_Protocol/DATA/assemblies/SRR5330501.transabyss k=32 name=SRR5330501.transabyss.fasta j=20 in="/home/orp/Oyster_River_Protocol/DATA/rcorr/SRR5330501.TRIM_1P.cor.fq /home/orp/Oyster_River_Protocol/DATA/rcorr/SRR5330501.TRIM_2P.cor.fq" l=32 s=32 n=2 SIMPLEGRAPH_OPTIONS="--no-scaffold" OVERLAP_OPTIONS="--no-scaffold" MERGEPATH_OPTIONS="--greedy" SRR5330501.transabyss.fasta-6.fa'
The minimum coverage of single-end contigs is 2.
The minimum coverage of merged contigs is 2.
warning: the seed-length should be at least twice k: k=32, s=32
Building the suffix array...
Building the Burrows-Wheeler transform...
Building the character occurrence table...
Mateless 52894022 100%
Unaligned 0
Singleton 0
FR 0
RF 0
FF 0
Different 0
Total 52894022
abyss-fixmate: error: All reads are mateless. This can happen when first and second read IDs do not match.
error: `SRR5330501.transabyss.fasta-3.hist': No such file or directory
Everything until then went fine! Do you know what the problem is?
The reads ID is this:
@MG00HS05:491:C7450ACXX:4:1101:1240:2223_forward/1
and
@MG00HS05:491:C7450ACXX:4:1101:1240:2223_reverse/2
These files were produced from fastq-dump. It seems that the problem is the naming, should be identical. So I should remove the forward and reverse part. Do you have a simple way to do that?
Can i restart the pipeline from the checkpoint above? Or do I have to run it from the start?
The text was updated successfully, but these errors were encountered:
You can try this fix. Just replace the read1/2 and output file names for your purposes.
sed "s/_forward//g" $READ1 > new_reads.1.fq
sed "s/_reverse//g" $READ2 > new_reads.2.fq
The ORP is checkpointed so you should be able to just restart it and it will pick up at the last checkpoint it passed. Note that you will want to rename the *TRIM_*P.cor.fq reads or it will resume and give you the same error.
Here is the CMD output:
Everything until then went fine! Do you know what the problem is?
The reads ID is this:
These files were produced from fastq-dump. It seems that the problem is the naming, should be identical. So I should remove the forward and reverse part. Do you have a simple way to do that?
Can i restart the pipeline from the checkpoint above? Or do I have to run it from the start?
The text was updated successfully, but these errors were encountered: