Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after Single Genomic Aplification
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA379528
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资源简介：
We compared Next Generation Sequencing (NGS) with De Novo assembly and Sanger sequencing for their ability to distinguish clonal and non clonal samples after SGA
创建时间：
2017-03-17
