Closed susheelbhanu closed 4 years ago
Hi, It seems the genome coverage in that sample is zero or too low.
Cheers, Tunde
Hi Tunde,
How is the genome coverage calculated? Because I used a different coverage estimation method, and according to it, the same is 12X.
Could you please clarify?
Thanks!
Could you confirm that majority of your contigs have coverage > 0?
Hi,
Please see attached the contigs coverage file.
Thank you! B12_maxbin.001.contigs.fa.txt
Hi, it is not clear what the columns are in the attached file. What are they? I assume the 2nd column is contig length. Right?
yeah sorry.. the 2nd is length and the 3rd the coverage per contig
Is there a way you can send across the fastq file and in question and also the genome?
Thanks.. i'm on a train at the moment, so will send them to you Wednesday, if that's ok?! thanks again for the help!
Thanks.. i'm on a train at the moment, so will send them to you Wednesday, if that's ok?! thanks again for the help!
Sure. Send it whenever you are ready
Hi,
I'm running a grid single command as follows and get the following error:
grid single -r . -e fastq -o grid_output -g ../B12_maxbin.001.contigs.fa-fixed.fa -n 2
Any thoughts on why this is occuring?
Thank you!