Strain Information for all 40 HPIV-1 Genomes Sequenced.

*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.

*本批序列仍存在部分序列缺口。若某基因的编码区存在序列缺口，则该基因序列将不用于对应基因的编码区（开放阅读框，ORF）分析。
#样本类型用于标识该基因组的测序来源：临床分离株（I）、临床标本（S），或二者混合来源（I和S）。
a. 序列HPIV-1/WI/629-005/1997在核苷酸位点8270–9308、9520–10136、10172–10175、10640–10701、11474–11883、12475–12507及13196–13590处存在序列缺口。
b. 序列HPIV-1/WI/629-D00057/2009在核苷酸位点2199–2262、8172–8653、9750–10223及11823–11926处存在序列缺口。
c. 序列HPIV-1/WI/629-D01250/2009在核苷酸位点8271–8802处存在序列缺口。
d. 序列HPIV-1/WI/629-D01774/2009在核苷酸位点2301–2326、3671–3772、4070–4253及11906–13627处存在序列缺口。
e. 序列HPIV-1/WI/629-D02211/2010在核苷酸位点2995–3041、3676–3740、6408–7517及15157–15445处存在序列缺口。