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. 2018 Sep 19;17(2):540–549. doi: 10.1111/pbi.12997

Table 4.

NLR coverage in commercial potato variety Innovator following RenSeq and whole‐genome sequencing

Innovator
RenSeq Whole‐genome sequencing
Total gigabase pairs 0.778 69.04 28.99 19.33 9.3 0.777
Gene name RenSeq_all sub88 [all] sub36 sub24 sub12 sub01
Rpi‐R1 ΔT4109 100.00 100.00 100.00 99.34 89.76 7.36
Rpi‐R2‐like 100.00 100.00 100.00 95.13 93.12 20.48
Rpi‐R3a 100.00 100.00 98.29 97.04 91.22 11.33
Rpi‐R3b 97.72 99.22 97.30 96.96 71.63 0.00
Rpi‐R3b G1696/G3111 100.00 100.00 100.00 100.00 83.15 0.00

DRenSeq was conducted on potato variety Innovator and compared to whole‐genome sequencing (WGS). For the comparison between RenSeq and WGS, subsamples of WGS reads were obtained. The sequence volume of WGS reads compared to RenSeq reads are shown in gigabases and x sequence volume [sub 01 =  equal amount to RenSeq; sub12 = 12× WGS compared to RenSeq; sub24 = 24× WGS compared to RenSeq; sub36 = 36× WGS compared to RenSeq; sub88 = 88× WGS compared to RenSeq (in this case all WGS data). The IDs of the Resistance to Phytophthora infestans (Rpi) nucleotide‐binding, leucine‐rich‐repeat resistances are shown. The representation of individual, full‐length Rpi genes was calculated by extracting the sequence coverage of dRenSeq‐mapped reads to the reference coding DNA sequence (CDS). WGS reads were mapped under the same stringent mapping condition used for dRenSeq. Highlighted in green are Rpi genes that achieved 100% representation and are therefore classified as ‘present’.