Additional file 1 of New approach for genomic characterisation of equine sarcoid-derived BPV-1/-2 using nanopore-based sequencing

Additional file 1. Detailed information on the clinical samples and the corresponding sequence variants. Clinical samples were processed in three different sample batches. While the primer set used for the first batch proved highly successful, the fraction of BPV-specific reads in some of the samples was low, indicating significant off-target amplification. The higher specificity of the V2 primer set significantly increased the fraction of BPV-specific reads.