Figure 1

This data is the RLU output from a luminometer of individual wells of cells transfected with the pGL3-PUb plasmid sorted by cell line.

Figure 2

This data is the titre in plaque forming units per ml recovered from PP9ad cells infected with rTOSV at an MOI of 5 over 72 hours.

Figure 5

A and B data shows the normalised RLU output from a luminometer of individual wells of cells transfected with both pPUb-RLuc and pGL3-PUb and shown combinations of dsRNA. C shows relative gene expression from three replicate qRT-PCRs calculated according to the method stated.

Figure 6

B shows the ratio of RLUs recorded for the anti nucleocapsid antibody against the Tubulin antibody after transfection with the stated dsRNA. C shows the titre in plaque forming units per ml of virus recovered after 48 hours after transfection witht he stated dsRNA.

Figure 7

This data shows the total count of reads mapping to each viral genome segment in both antigenomic +ve (AG) and genomic -ve (G) sense for each sequencing replicate and infected and mock infected conditions.

Figure 8

This data shows the size distribution of the lengths of RNAs mapping to the genomic segments as a percentage of total for each sequencing replicate. positive numbers map to the antigenome (AG) and negative to the genome (G).

Figure 9

This data shows records the coverage of each nucleotide in the genome as a percentage of the total for each sequencing replicate. positive titled numbers mapped to the antigenome and negative titled to the genome.

Figure 10

This data shows the start nucleotide of 21nt small RNAs which were identical accross the three sequencing replicates as a percentage of total.

Figure 11

This shows the z scores calculated for the overlaps of each sequencing replicate by genomic segment.