QUESTIONS AND ANSWERS
,1. How do we study microbes present in gut?: 16S
Sequencing Protocol look at specific sequences on a gene that
codes for ribosomes
They code for protein
This region is conserved
2. 16S Data Visualization - Cluster Analysis: shows variation
between biological samples each sphere represents the
microbiota of a biologic samples distance represents
dissimilarities in sequence between microbial samples
Beta Diversity
3. Alpha Diversity: relative abundance of bacteria/ bacterial
diversity within a bio- logic sample
how many microbes are in my poop?
each bar represents a biological sample
each color within a bar is a different phylum of a microbe and
shows relative abundance
4. Beta Diversity: differences in microbiota between people, body
regions, biologi- cal samples
how different is your microbiota from mine?
, micro biomes that share sequence similarities (likeness) are
clustered together
5. Bacterial Sequence Database Analysis: extract DNA from
poop samples sequence the DNA
compare the DNA sequences to a database known as the
bacterial sequences determine bacterial species and quantity of
each species
more sequences = more bacterial species
shows only alpha diversity because shows how many species of
microbes are in each group but doesn't show similarity between
the 2
6. Opening reading frame (ORF): stretch of DNA or RNA
consisting of codons for amino acids uninterrupted by a stop
codon (potentially protein coding region)
ORF is where we find the start codon and this is where the
protein begins being translated