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1.Here, we use a primer set designed to detect the full taxonomic diversity of fungal small subunit ribosomal RNAgenes
2.Group-specifc environmental PCR followed by cloning and gene library construction provides a means of comparing subsets of microbial diversity between environ-ments, detecting low-abundance microbes and improvings ampling effciency

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detecting low-abundance microbes and improving sampling effciency
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1.Here, we use a primer set designed to detect the full taxonomic diversity of fungal small subunit ribosomal RNAgenes
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