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. 2018 Jun 19;5:180119. doi: 10.1038/sdata.2018.119

Table 1. Summary of the obtained read counts from long-read sequencing aligned to the PRV genome.

Samplea Number of PRV readsb Number of mapped readsc
MinION-Cap-selected 120394 131223
MinION-cDNA 44006 47363
MinION-RNA 29832 30667
Sequel 12555 13481
RSII-PolyA-amplified-1h 6956 6956
RSII-PolyA-amplified-4h 22958 22958
RSII-PolyA-amplified-8h 46147 46147
RSII-PolyA-amplified-1, 2, 4, 6, 8h-Bluepippin 0.8kb-5kb+ 1077 1077
RSII-PolyA-amplified-1, 2, 4, 6, 8h-Bluepippin 0.8-2kb 7728 7728
RSII-PolyA-amplified-1, 2, 4, 6, 8h-Bluepippin 2-3kb 6131 6131
RSII-PolyA-amplified-1, 2, 4, 6, 8h-Bluepippin 3-5kb 3705 3705
RSII-PolyA-amplified-1, 2, 4, 6, 8h-Bluepippin 5kb+ 4061 4061
RSII-PolyA-amplified-1, 4, 8h,-Manual Gel 1-2kb 3822 3822
RSII-PolyA-amplified-1h-Manual Gel 3kb+ 3110 3110
RSII-PolyA-amplified-1h-Manual Gel 2-3kb 483 510
RSII-PolyA-amplified-4h-Manual Gel 3kb+ 2645 2928
RSII-PolyA-amplified-4h-Manual Gel 2-3kb 14348 15708
RSII-PolyA-amplified-8h-Manual Gel 3kb+ 3443 3765
RSII-PolyA-amplified-8h-Manual Gel 2-3kb 1608 1765
RSII-random-amplified-1, 2, 4, 6, 8h 1804 1953
RSII-random-amplified-1h 2327 2485
RSII-random-amplified-4h 7202 7629
RSII-random-amplified-8h 11452 12259
RSII-random-amplified-1, 4, 8h,-Manual Gel 3kb+ 1778 1855
RSII-random-amplified-1, 4, 8h,-Manual Gel 1-2kb 2218 2425
RSII-random-amplified-1, 4, 8h,-Manual Gel 2-3kb 3393 3627
RSII-PolyA-non amplified-1h (1st) 74 81
RSII-PolyA-non amplified-1h (2nd) 7392 7440
RSII-PolyA-non amplified-2h (1st) 124 125
RSII-PolyA-non amplified-2h (2nd) 12944 13121
RSII-PolyA-non amplified-4h (1st) 1369 1574
RSII-PolyA-non amplified-4h (2nd) 1023 1054
RSII-PolyA-non amplified-6h (1st) 2144 2269
RSII-PolyA-non amplified-6h (2nd) 10151 10231
RSII-PolyA-non amplified-8h (1st) 219 237
RSII-PolyA-non amplified-8h (2nd) 7915 8015
RSII-PolyA-non amplified-12h (1st) 935 1002
RSII-PolyA-non amplified-12h (2nd) 12731 12864

aType of the samples.

bTotal number of PRV-specific reads.

cTotal number of reads mapped to the PRV genome. (There is an approximately 15 kb-long inverted repeat sequence region in the PRV genome, therefore those reads which map to this location occur in duplicate in row c).