I have two NGS files from an NGS company corresponding to the sequencing data from a tumor sample as follows:
I have downloaded the genome for MCPyV as a file called “MCPYV_Sequence.fasta”
I have downloaded the Hg38 as a file called “hg_38.fa”
I have input the host genome as hg_38.fa, the viral genome as “ MCPYV_Sequence.fasta” and the sequence data as both FASTQ files.
I run the assembly in the cloud, and I receive back an error stating that the assembly as failed.
What am I doing wrong?