SRX1896592 206.1.1plaB4.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539612 SAMN05335457 206.1.1plaB4.Y2011 AMPLICON METAGENOMIC PCR 100 0 Application Read Forward 1 Illumina HiSeq 2500 SRX1896593 260.1.1plaB3.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539613 SAMN05335458 260.1.1plaB3.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896594 671.2plaB7.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539614 SAMN05335467 671.2plaB7.Y2011 AMPLICON METAGENOMIC PCR 100 0 Application Read Forward 1 Illumina HiSeq 2500 SRX1896595 671.dry.2colB7.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539615 SAMN05335468 671.dry.2colB7.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896596 705.3.1plaB28.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539616 SAMN05335469 705.3.1plaB28.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896597 750.1plaB11b.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539617 SAMN05335470 750.1plaB11b.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896598 750.2plaB11b.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539618 SAMN05335471 750.2plaB11b.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896599 750.dry.2colB11b.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539619 SAMN05335472 750.dry.2colB11b.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896600 770.3.2plaB3.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539620 SAMN05335473 770.3.2plaB3.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896601 782.1plaB15.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539621 SAMN05335474 782.1plaB15.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896602 820.1plaB25.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539622 SAMN05335475 820.1plaB25.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896603 821.1plaB17.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539623 SAMN05335476 821.1plaB17.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896604 263.1plaB6.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539624 SAMN05335459 263.1plaB6.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896605 896.1plaB14.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539625 SAMN05335477 896.1plaB14.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896606 896.2plaB14.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539626 SAMN05335478 896.2plaB14.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896607 896.dry.2colB14.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539627 SAMN05335479 896.dry.2colB14.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896608 263.2plaB6.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539628 SAMN05335460 263.2plaB6.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896610 263.dry.2colB6.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539630 SAMN05335461 263.dry.2colB6.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896611 271.1plaB13.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539629 SAMN05335462 271.1plaB13.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896612 328.1plaB12b.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539632 SAMN05335463 328.1plaB12b.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896613 58.1plaB10.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539631 SAMN05335464 58.1plaB10.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896614 652.1plaB9.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539633 SAMN05335465 652.1plaB9.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500 SRX1896615 671.1plaB7.Y2011 SRP077863 PRJNA327018 Grassland soil was collected from the western Swiss Alps study area. The total community DNA was extracted from soil samples using the MoBio PowerSoil DNA extraction kit in triplicate and combined. PCR of the V5 region of the bacterial 16S rRNA gene was done in 4x using barcoded 784DEG and 880RDEG primers, and replicate PCR products were combined prior to purification with MinElute. Paired-end 100bp sequencing was done on the HiSEQ Illumina platform. The primer barcodes were removed, and PandaSeq was used to obtain consensus reads from each paired-end reads. SRS1539634 SAMN05335466 671.1plaB7.Y2011 AMPLICON METAGENOMIC PCR Illumina HiSeq 2500