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The total DNA concentration was adjusted to 30 ng L 1 ( Following total DNA extraction, the fungal ITS region was amplified using the eukaryotic primers ITS1F primer (5-CTTGGTCATTTAGAGGAAGTAA-3) and ITS2R (5-GCTGCGTTCTTCATCGATGC-3) ( Data Processing Single-end reads were generated (i.e., 400 bp/600 bp for fungi and 1,000 bp/1,200 bp for bacteria), followed by qualitative filtering and merging of raw reads by Cutadapt version 1.9.1
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Sequence data were analyzed using CLC Genomic Workbench 9.5 (QIAGEN, Hilden, Germany) as described 19
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