Hello,
I have a couple of questions.
1) I was thinking of using Racon to polish the smartdenovo assembly. Racon suggests to use these reads:
racon [options ...]
<sequences>
input file in FASTA/FASTQ format (can be compressed with gzip)
containing sequences used for correction
<overlaps>
input file in MHAP/PAF/SAM format (can be compressed with gzip)
containing overlaps between sequences and target sequences
<target sequences>
input file in FASTA/FASTQ format (can be compressed with gzip)
containing sequences which will be corrected
for the first sequences, I can give illumina reads as the input , I am not sure what would be the best input for the second sequnces as smartdenovo does not make any mhap files like other assemblers like Canu and for the third sequences I will input the .cns file generated by smartdenovo assembly.
Can you please help me out what needs to go in the input files for the overlaps?
2) is there a better polishing tool other than Racon for Smartdenovo assembly? Note : I have used long reads from both PacBio and Nanopore for my assembly
I am not sure how to run Racon, but from your description, PAF and SAM file can be generated by minimap2. I used to polish the contigs with Quiver and pilon.
Hello, I have a couple of questions. 1) I was thinking of using Racon to polish the smartdenovo assembly. Racon suggests to use these reads: racon [options ...]
for the first sequences, I can give illumina reads as the input , I am not sure what would be the best input for the second sequnces as smartdenovo does not make any mhap files like other assemblers like Canu and for the third sequences I will input the .cns file generated by smartdenovo assembly.
Can you please help me out what needs to go in the input files for the overlaps? 2) is there a better polishing tool other than Racon for Smartdenovo assembly? Note : I have used long reads from both PacBio and Nanopore for my assembly
Thanks heaps in advance S