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. 2016 Nov 9;11(11):e0165880. doi: 10.1371/journal.pone.0165880

Table 1. Primer sequences used for the present genome amplification.

Primer name Sequence (5′→3′) Polarity Regiona
Sydney2012-1F GTGAATGAAGATGGCGTCTAAC + 1–22
Sydney2012-1R GGTAAATCCTAGCACCAAACCT - 1045–1066
Sydney2012-2F TGATTGGACCTTCGCAGGCATAG + 871–893
Sydney2012-2R TCTAGCCTCTCATGGAGTAACC - 2055–2076
Sydney2012-3F CATCCATGATGCCCTCAGGT + 1660–1679
Sydney2012-3R GATTTGCTTGATAGGGACTCCG - 3148–3169
Sydney2012-4F GCAACCGAAGAGGACTTCTGTGAAG + 2813–2837
Sydney2012-4R TGAGGAGCCAGTGGGCGATGGAAT - 4497–4520
290 H GATTACTCCAGGTGGGACTCCAC + 4295–4317
290 I GATTACTCCAGGTGGGACTCAAC
290 J GATTACTCCAGGTGGGATTCAAC
290 K GATTACTCCAGGTGGGATTCCAC
G2SKR CCACCTGCATAACCATTGTACAT - 5367–5389
COG2F CARGARBCNATGTTYAGRTGGATGAG + 5003–5029
VN3T20 GAGTGACCGCGGCCGCT20 - Poly A

a Each sequence number of primer sets region is listed for Sydney 2012 strain (GenBank accession No. JX459908).