Hi,
I am trying to analyze RNA Modifications in Direct RNA-seq nanopore datasets. I performed the sequencing using rat cell line, so my reference is Rnor_6. I am trying to perform resquiggle on my Fast5s, but I get an error stating that Minimap failed to load reference genome Fasta. I used difference assemblies from NCBI and Ensemble with the extensions .fna or .fa but I am getting the same error. I got my files from Illumina's iGenome list and also tried from NCBI and Ensemble directly. I tried using the software Geneious to convert my .fna file to .Fasta but didn't help either. Can anyone point me to a potential issue or error I made? Even preprocessing using tombo preprocess command did not help. My Fast5s are basecalled using Guppy.
Thanks a lot
Hi, I am trying to analyze RNA Modifications in Direct RNA-seq nanopore datasets. I performed the sequencing using rat cell line, so my reference is Rnor_6. I am trying to perform resquiggle on my Fast5s, but I get an error stating that Minimap failed to load reference genome Fasta. I used difference assemblies from NCBI and Ensemble with the extensions .fna or .fa but I am getting the same error. I got my files from Illumina's iGenome list and also tried from NCBI and Ensemble directly. I tried using the software Geneious to convert my .fna file to .Fasta but didn't help either. Can anyone point me to a potential issue or error I made? Even preprocessing using tombo preprocess command did not help. My Fast5s are basecalled using Guppy. Thanks a lot