Skip to main content
. 2020 Oct 29;14(10):e0008781. doi: 10.1371/journal.pntd.0008781

Table 1. Specificity and sensitivity of the capture-based parasite DNA enrichment approach.

Isolate Pre-enrichment Theileria gDNA (%)a Total reads generatedb Total reads aligned Mean coveragec Specificity (%)d Sensitivity (%)e
BV115 1.94 12,174,316 11,952,650 146X 98.03 99.80
Marikebuni 3292 3.05 7,204,556 6,740,297 202X 96.47 97.70
Uganda 3645 0.92 5,687,838 5,313,295 157X 97.52 98.34
Buffalo_3081 1.72 6,080,972 5,446,541 160X 96.40 97.59

a Proportion of the original DNA sample that is composed of T. parva DNA, as measured by qPCR [36].

b Read length for BV115 was 101 bp and 250 bp for the other three strains.

c Estimation: (Total_reads_aligned*Mean_read_length)/genome_size. The genome size used was the sum of the nuclear and apicoplast reference genomes targeted.

d Percent reads generated that mapped to T. parva reference genome.

e Percent of the T. parva reference genome to which reads map.