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. 2021 Mar 30;13(4):583. doi: 10.3390/v13040583

Table 1.

RNA-Seq paired-end genome sequence data, including sequence depth coverage, GC content and genome size of the Bean yellow mosaic virus (BYMV), Pea seed-borne mosaic virus (PSbMV), Pea early browning virus (PEBV) and Cucumber mosaic virus (CMV) isolates used in this study for primer design and target template for TG-Seq verification.

Sample Host Virus Coverage (x) c No of Read Counts Mapping to the Virus GC Content Genome Size GenBank Accession
14BY a Lentil BYMV 2307 1,331,893 39.4% 9868 LC500882
13C Field pea PSbMV 718 507,189 41.5% 9852 SRR13206509
LY-2 b Faba bean PEBV-RNA1 3899 235,443 40.7% 7037 LC528622
LY-2 b Faba bean PEBV-RNA2 5606 1,252,888 42% 2604 LC528623
14C Faba bean CMV-RNA1 8774 318,290 45.3% 3215 SRR13197436
14C Faba bean CMV-RNA2 37,144 1,293,807 45.3% 2892 SRR13197436
14C Faba bean CMV-RNA3 10,615 260,700 47.1% 2188 SRR13197436

a = Genome sequence of PEBV as reported [29], b = BYMV as reported [30], 13C and 14C = new PSbMV and CMV genome sequences generated from this study. c = Average coverage depth across the genome (x) times. The three genomes missed a few nucleotides within the 5′UTR and 3′UTR genome regions but all the coding regions were intact.