Using blobology with Nanopore reads

[AdeAdigun]

I'm trying to use the metwrap blobology module to make blob plots but I keep getting the error"Unable to find proper fastq read pair in the format *_1.fastq and *_2.fastq" Is it possible to run this without pair ended read files? This is the line I ran:
metawrap blobology -a ./consensus.fasta -t 71 -o BLOBOLOGY --bins ./bin_refinement/metawrap_90_10_bins ./5_cat.fastq