<HashMap><database>NODE</database><scores/><additional><omics_type>Other</omics_type><submitter>Ting Zhu</submitter><technology_type>AMPLICON</technology_type><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00002212</full_dataset_link><experiment_platform>Illumina HiSeq 2000</experiment_platform><experiment_library_selection>RANDOM</experiment_library_selection><experiment_library_layout>Paired</experiment_library_layout><sample_count>190</sample_count><taxonomy>['soil metagenome']</taxonomy><experiment_protocol>The V4 region of 16S rRNA gene was amplified using the primer pair 515F (5’-GTGYCAGCMGCCGCGGTAA-3’) and 806R (5’-GGACTACNVGGGTWTCTAAT-3’) [1, 2]. A unique 12-bp barcode and a 2-bp linker (5’-TC-3’) were inserted between the barcode and the forward primer (5’-NNNNNNNNNNNNTC-515F-3’) to tag each PCR product. Sequencing was performed on the HiSeq platform (Illumina, San Diego, USA) to generate 250 base-pair paired-end reads.</experiment_protocol><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>16S rRNA gene amplicon sequencing of saltmarsh soil</name><description>16S rRNA gene amplicon sequencing of saltmarsh soil</description><dates><publication>2021-09-16</publication><submission>2020-01-13</submission></dates><accession>OEX00002212</accession><cross_references><NODE>OEP00000745</NODE></cross_references></HashMap>