Hi there,
I had a purified PCR product (16S mixed bacterial community) and produced three different libraries from the same PCR product. These three libraries were then run through the Illumina MiSeq to have a look at the repeatability of library prep and down stream analysis.
After processing, the communities of the three libraries look very similar visually in a stacked bar and relative abundances look comparable (e.g. The relative abundance of Firmicutes is 44.99, 45.34 and 46.46% across the three samples) but does anyone know if there is anyway of analysing this statistically? The sample is from the rumen of cattle and contains many different genera.
I appreciate any help anyone can offer. This is my first post here so I apologise if I've missed any details.
I had a purified PCR product (16S mixed bacterial community) and produced three different libraries from the same PCR product. These three libraries were then run through the Illumina MiSeq to have a look at the repeatability of library prep and down stream analysis.
After processing, the communities of the three libraries look very similar visually in a stacked bar and relative abundances look comparable (e.g. The relative abundance of Firmicutes is 44.99, 45.34 and 46.46% across the three samples) but does anyone know if there is anyway of analysing this statistically? The sample is from the rumen of cattle and contains many different genera.
I appreciate any help anyone can offer. This is my first post here so I apologise if I've missed any details.
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