Strain Information for all 40 HPIV-1 Genomes Sequenced.
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*These sequences still have some gaps. Gene sequences with gaps in the coding region were not used for the coding region (ORF) analysis for that specific gene. #The sample type indicates whether the genome was sequenced from a clinical isolate (I), a clinical specimen (S) or a combination of the two (I and S). aSequence of HPIV-1/WI/629-005/1997 has gaps at nts 8270–9308, 9520–10136, 10172–10175, 10640–10701, 11474–11883, 12475–12507 and 13196–13590. bSequence of HPIV-1/WI/629-D00057/2009 has gaps at nts 2199–2262, 8172–8653, 9750–10223, and 11823–11926. cSequence of HPIV-1/WI/629-D01250/2009 has gaps at nts 8271–8802. dSequence of HPIV-1/WI/629-D01774/2009 has gaps at nts 2301–2326, 3671–3772, 4070–4253, and 11906–13627. eSequence of HPIV-1/WI/629-D02211/2010 has gaps at nts 2995–3041, 3676–3740, 6408–7517, and 15157–15445.



