SRX1050253 Gut_DB11 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954496 SAMN03758585 Gut_DB11 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050254 Gut_DB12 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954494 SAMN03758586 Gut_DB12 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050255 Gut_DB13 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954495 SAMN03758587 Gut_DB13 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050256 Gut_DB14 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954493 SAMN03758588 Gut_DB14 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050258 Gut_DB22 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954492 SAMN03758590 Gut_DB22 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050259 Gut_DB23 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954491 SAMN03758591 Gut_DB23 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050260 Gut_DB24 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954489 SAMN03758592 Gut_DB24 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050261 Gut_DS11 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954487 SAMN03758593 Gut_DS11 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050262 Gut_DS12 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954488 SAMN03758594 Gut_DS12 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050263 Gut_DS13 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954486 SAMN03758595 Gut_DS13 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050264 Gut_DS14 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954485 SAMN03758596 Gut_DS14 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050265 Gut_DS21 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954484 SAMN03758597 Gut_DS21 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050266 Gut_DS22 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954483 SAMN03758598 Gut_DS22 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050267 Gut_DS23 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954482 SAMN03758599 Gut_DS23 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050268 Gut_DS24 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954481 SAMN03758600 Gut_DS24 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050269 Gut_DF11 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954480 SAMN03758601 Gut_DF11 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050270 Gut_DF12 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954479 SAMN03758602 Gut_DF12 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050271 Gut_DF13 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954478 SAMN03758603 Gut_DF13 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050272 Gut_DF14 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954477 SAMN03758604 Gut_DF14 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050273 Gut_DF21 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954476 SAMN03758605 Gut_DF21 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050274 Gut_DF22 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954475 SAMN03758606 Gut_DF22 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050275 Gut_DF23 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954474 SAMN03758607 Gut_DF23 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050276 Gut_DF24 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954473 SAMN03758608 Gut_DF24 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050277 Gut_AB11 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954472 SAMN03758609 Gut_AB11 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050278 Gut_AB12 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954471 SAMN03758610 Gut_AB12 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050279 Gut_AB13 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954470 SAMN03758611 Gut_AB13 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050280 Gut_AB14 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954469 SAMN03758612 Gut_AB14 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050281 Gut_AB21 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954468 SAMN03758613 Gut_AB21 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050282 Gut_AB22 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954467 SAMN03758614 Gut_AB22 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050283 Gut_AB23 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954466 SAMN03758615 Gut_AB23 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050284 Gut_EB11 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954465 SAMN03758616 Gut_EB11 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050285 Gut_EB12 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954464 SAMN03758617 Gut_EB12 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050286 Gut_EB13 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954463 SAMN03758618 Gut_EB13 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050287 Gut_EB14 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954462 SAMN03758619 Gut_EB14 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050288 Gut_EB21 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954461 SAMN03758620 Gut_EB21 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050289 Gut_EB22 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954460 SAMN03758621 Gut_EB22 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050290 Gut_EB23 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954459 SAMN03758622 Gut_EB23 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq SRX1050291 Gut_EB24 SRP059174 PRJNA285665 "This analysis was done as in Caporaso et al 2011 Genome research. The PCR primers F515 and R806 were developed against the V4 region of the 16S rRNA, both bacteria and archaea, which we determined would yield optimal community clustering with reads of this length The reverse PCR primer is barcoded with a 12-base error-correcting Golay code to facilitate multiplexing of up to 1,500 samples per lane, and both PCR primers contain sequencer adapter regions." SRS954458 SAMN03758623 Gut_EB24 AMPLICON METAGENOMIC PCR 300 0 Application Read Forward 1 1 Application Read Reverse 151 Illumina MiSeq