SRX4326977 NODDKO-M-2.72517 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489154 SAMN09519577 NODDKO-M-2.72517 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326978 NODDKO-M-1.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489155 SAMN09519576 NODDKO-M-1.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326979 NODDKO-M-3.9717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489156 SAMN09519579 NODDKO-M-3.9717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326980 NODDKO-M-2.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489157 SAMN09519578 NODDKO-M-2.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326981 NODDKO-M-4.82817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489158 SAMN09519581 NODDKO-M-4.82817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326982 NODDKO-M-3.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489159 SAMN09519580 NODDKO-M-3.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326983 WT-F-1.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489160 SAMN09519583 WT-F-1.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326984 WT-F-1.81817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489161 SAMN09519582 WT-F-1.81817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326985 WT-F-2.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489162 SAMN09519585 WT-F-2.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326986 WT-F-2.81817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489163 SAMN09519584 WT-F-2.81817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326987 NODDKO-M-1.82817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489164 SAMN09519575 NODDKO-M-1.82817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326988 NODDKO-M-1.9717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489165 SAMN09519574 NODDKO-M-1.9717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326989 NODDKO-F-1.72517 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489166 SAMN09519567 NODDKO-F-1.72517 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326990 NODDKO-F-1.9617 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489167 SAMN09519566 NODDKO-F-1.9617 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326991 NODDKO-F-2.9617 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489168 SAMN09519569 NODDKO-F-2.9617 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326992 NODDKO-F-1.101817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489169 SAMN09519568 NODDKO-F-1.101817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326993 NODDKO-F-2.101817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489170 SAMN09519571 NODDKO-F-2.101817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326994 NODDKO-F-2.72517 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489171 SAMN09519570 NODDKO-F-2.72517 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326995 NODDKO-F-4.9617 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489172 SAMN09519573 NODDKO-F-4.9617 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326996 NODDKO-F-3.9617 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489173 SAMN09519572 NODDKO-F-3.9617 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326997 WT-M-4.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489174 SAMN09519594 WT-M-4.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326998 WT-M-5.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489175 SAMN09519595 WT-M-5.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4326999 WT-F-3.81817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489176 SAMN09519586 WT-F-3.81817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327000 WT-F-3.101717 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489177 SAMN09519587 WT-F-3.101717 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327001 WT-F-4.101817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489178 SAMN09519588 WT-F-4.101817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327002 WT-F-5.101817 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489179 SAMN09519589 WT-F-5.101817 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327003 WT-M-1.71217 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489180 SAMN09519590 WT-M-1.71217 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327004 WT-M-1.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489181 SAMN09519591 WT-M-1.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327005 WT-M-2.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489182 SAMN09519592 WT-M-2.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327006 WT-M-3.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489183 SAMN09519593 WT-M-3.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327007 WT-M-8.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489184 SAMN09519597 WT-M-8.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX4327008 WT-M-6.82117 SRP151673 PRJNA478558 Total DNA was extracted using Mo-Bio (now Qiagen) PowerFecal kit. Sample libraries were prepared and analyzed by barcoded amplicon sequencing. In brief, the purified DNA was amplified on the V4 region of the 16S rRNA genes via PCR using the following primers: F319 (5-ACTCCTACGGGAGGCAGCAGT-3) and R806 (5-GGACTACNVGGGTWTCTAAT-3). High-throughput sequencing was performed with Illumina MiSeq paired end 250-bp run. SRS3489185 SAMN09519596 WT-M-6.82117 AMPLICON METAGENOMIC PCR Illumina MiSeq