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Use of Massively Parallel Ultradeep Pyrosequencing To Characterize the Genetic Diversity of Hepatitis B Virus in Drug-Resistant and Drug-Naive Patients and To Detect Minor Variants in Reverse Transcriptase and Hepatitis B S Antigen

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Figure

TABLE 1. Sequences and positions of primers used for UDPSof HBV
TABLE 2. Comparison of UDPS, DR v2, and direct sequencing for HBV from eight patients under treatment
TABLE 2—Continued
FIG. 1. Frequency of substitutions within RT (A) and HBsAg (B) detected by UDPS in 13 HBV-positive patients
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