Robert Vaser

Results 370 comments of Robert Vaser

Are you trying to polish contigs or correct reads with each other? Please provide me with your command and descriptions of input parameters.

I have trouble understanding your description. What is in the file?

Lets start from the beginning. You have some ONT data, is it DNA or RNA? Are you trying to assemble the sequenced genome or just increase the read accuracy?

If you want to polish your reads with racon you should run the following: ```bash minimap2 -ax ava-ont --dual=yes > alignments.sam racon -f alignments.sam > polished_reads.fasta ``` If you want...

I am running `dnadiff ` which creates several files. In *.report file is the summary of the comparison.

Both files need to be in fasta format. Thank you for your kind words :)

I have been using this one: https://github.com/marbl/MUMmer3. Did not yet try v4. You can download it with `git clone https://github.com/marbl/MUMmer3` and run `make` in the created directory.

Hi Robert, the problem is that you have a sequence in `trimmed.fastq` and `reference.fa` that share a name. Try renaming your reference reads, rerun the minimap2 command and run racon...