I am kindly writing to you to learn, whether there is a way to extract the mismatched nucleotide frequency information out of Epinano_Variants.pyoutput.
This would be the information of mismatch frequencies, not cumulative for all nucleotides, but per nucleotide, such as:
Hi @kaltinel i believe that what you are looking for is EpiNano_RMS.py, which is available in the nanoRMS repository. The usage of this script is explained in the README. Best, Eva
Hi,
I hope you are well.
I am kindly writing to you to learn, whether there is a way to extract the mismatched nucleotide frequency information out of
Epinano_Variants.py
output. This would be the information of mismatch frequencies, not cumulative for all nucleotides, but per nucleotide, such as:Looking forward to hearing from your side, thanks!