SRX4393127 cDNA Biofilm cathode 3 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548663 cDNA Biofilm cathode 3 cDNA Biofilm cathode 3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393128 cDNA Biofilm cathode 2 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548661 cDNA Biofilm cathode 2 cDNA Biofilm cathode 2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393129 DNA Biofilm cathode 2 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548662 DNA Biofilm cathode 2 DNA Biofilm cathode 2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393130 DNA Biofilm cathode 1 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548660 DNA Biofilm cathode 1 DNA Biofilm cathode 1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393131 Inoculum 2 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548666 Inoculum 2 Inoculum 2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393132 Inoculum 1 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548665 Inoculum 1 Inoculum 1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393133 cDNA Biofilm cathode 1 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548664 cDNA Biofilm cathode 1 cDNA Biofilm cathode 1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393134 DNA Liquid SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548667 DNA Liquid DNA Liquid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393135 DNA Biofilm cathode 4 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548668 DNA Biofilm cathode 4 DNA Biofilm cathode 4 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393136 DNA Biofilm cathode 3 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548669 DNA Biofilm cathode 3 DNA Biofilm cathode 3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4393137 cDNA Biofilm cathode 4 SRP153784 bp0 Amplification of the hypervariable V4 region of the 16S rRNA gene. Dual-indexed Illumina compatible libraries were produced in a single PCR step. Fusion primers with target-specific positions and Fluidigm CS oligos (51 ends) were used for the primary PCR. Secondary, PCR targeting the CS oligos was use to add sequences necessary for Illumina sequencing and unique indexes. Invitrofen SequalPrep DNA normalization plates were used with PCR products. The pooled samples were sequenced using an Illumina MiSeq flow cell. SRS3548670 cDNA Biofilm cathode 4 cDNA Biofilm cathode 4 AMPLICON METAGENOMIC PCR Illumina MiSeq