You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hello, I'm using HASLR with nanopore and Illumina data to assemble a P. falciparum genome.
All nanopore data has around ~50x coverage.
All Illumina short reads are set as 2 paired-end fastq files (the paired-end doesn't matter for haslr, I believe?)
I used this command: haslr.py -t 10 -o pfalciparum -g 23m -l nanopore_data.fasta nanopore -s illumina_data.fasta
The resulting asm.final.fa contains about 10 million base pairs, which is much shorter than the expected 23 million base pairs for plasmodium falciparum. I've run this on several different nanopore samples and gotten the same result: a much shorter assembly than expected.
Do you have any suggestions? Thank you so much.
The text was updated successfully, but these errors were encountered:
Hello,
I have similar problem. ONT reads with average x50 coverage with Raven and Smartdenovo gave assemblies 750-780M with BUSCOs above 98%. Using ONT and Illumina reads in HASLR resulted in much shorter assembly c. 580M.
Did anybody solve this issue?
Hello, I'm using HASLR with nanopore and Illumina data to assemble a P. falciparum genome.
All nanopore data has around ~50x coverage.
All Illumina short reads are set as 2 paired-end fastq files (the paired-end doesn't matter for haslr, I believe?)
I used this command: haslr.py -t 10 -o pfalciparum -g 23m -l nanopore_data.fasta nanopore -s illumina_data.fasta
The resulting asm.final.fa contains about 10 million base pairs, which is much shorter than the expected 23 million base pairs for plasmodium falciparum. I've run this on several different nanopore samples and gotten the same result: a much shorter assembly than expected.
Do you have any suggestions? Thank you so much.
The text was updated successfully, but these errors were encountered: