SRX5182960 Ana53 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189756 Ana53 Ana53 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182961 Ana54 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189761 Ana54 Ana54 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182962 Ana55 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189757 Ana55 Ana55 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182963 Ana56 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189758 Ana56 Ana56 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182964 Ana58 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189759 Ana58 Ana58 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182965 Ana59 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189760 Ana59 Ana59 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182966 Ana60 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189762 Ana60 Ana60 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182967 Ana61 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189764 Ana61 Ana61 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182968 Ana62 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189763 Ana62 Ana62 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182969 Ana63 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189765 Ana63 Ana63 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182970 CHWR38 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189766 CHWR38 CHWR38 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182971 CHWR37 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189767 CHWR37 CHWR37 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182972 CHIR36 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189768 CHIR36 CHIR36 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182973 CHIR35 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189769 CHIR35 CHIR35 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182974 CHIR34 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189770 CHIR34 CHIR34 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182975 CHIR33 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189771 CHIR33 CHIR33 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182976 CHIR32 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189772 CHIR32 CHIR32 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182977 CHIR31 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189777 CHIR31 CHIR31 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182978 CHWR40 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189773 CHWR40 CHWR40 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182979 CHWR39 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189774 CHWR39 CHWR39 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182980 Ana11 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189775 Ana11 Ana11 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182981 Ana10 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189776 Ana10 Ana10 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182982 Ana13 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189778 Ana13 Ana13 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182983 Ana12 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189779 Ana12 Ana12 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182984 UM1WR25 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189780 UM1WR25 UM1WR25 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182985 UM1WR24 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189781 UM1WR24 UM1WR24 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182986 UM1WR27 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189782 UM1WR27 UM1WR27 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182987 UM1WR26 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189783 UM1WR26 UM1WR26 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182988 Ana15 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189784 Ana15 Ana15 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182989 Ana14 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189785 Ana14 Ana14 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182990 UMWR04 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189786 UMWR04 UMWR04 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182991 UMWR08 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189787 UMWR08 UMWR08 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182992 UMWR09 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189788 UMWR09 UMWR09 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182993 CHWR41 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189789 CHWR41 CHWR41 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182994 CHWR42 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189790 CHWR42 CHWR42 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182995 CHIR29 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189791 CHIR29 CHIR29 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182996 CHIR30 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189792 CHIR30 CHIR30 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182997 CHWR45 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189793 CHWR45 CHWR45 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182998 Ana19 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189794 Ana19 Ana19 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5182999 UM1WR20 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189795 UM1WR20 UM1WR20 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183000 UM1WR21 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189796 UM1WR21 UM1WR21 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183001 Ana66 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189797 Ana66 Ana66 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183002 Ana67 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189798 Ana67 Ana67 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183003 Ana64 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189800 Ana64 Ana64 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183004 Ana65 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189799 Ana65 Ana65 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183005 Ana70 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189801 Ana70 Ana70 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183006 CHIR28 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189802 CHIR28 CHIR28 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183007 Ana68 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189803 Ana68 Ana68 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183008 Ana69 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189804 Ana69 Ana69 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183009 UM1WR22 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189805 UM1WR22 UM1WR22 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183010 UMWR05 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189806 UMWR05 UMWR05 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183011 UMWR02 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189807 UMWR02 UMWR02 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183012 UMWR03 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189808 UMWR03 UMWR03 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183013 Ana18 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189809 Ana18 Ana18 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183014 UMWR01 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189810 UMWR01 UMWR01 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183015 Ana16 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189811 Ana16 Ana16 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183016 Ana17 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189812 Ana17 Ana17 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183017 CHWR43 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189813 CHWR43 CHWR43 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183018 UMWR06 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189814 UMWR06 UMWR06 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183019 UMWR07 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189815 UMWR07 UMWR07 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183020 CHWR44 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189816 CHWR44 CHWR44 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX5183021 UM1WR23 SRP174536 bp0 The hypervariable V4 region of 16S rRNA library was constructed by following Illumina MiSeq protocol. Briefly, the protocol included a first stage amplicon PCR step involving 0.2 M concentrations of primers 515F (forward) and 806R (reverse). Sequences were demultiplexed and depleted of Illumina barcodes and primers by using MiSeq reporter and Trimmomatic software SRS4189817 UM1WR23 UM1WR23 AMPLICON METAGENOMIC PCR Illumina MiSeq