Term omics refers to
a suite of technologies used in biology and medicine to comprehensively characterize and quantify pools of biological molecules in living systems
4 categories of omics
genomics
proteomics
metabolomics
transcriptomics
Genomics
study of an organisms entire genome - all DNA
Proteomics
large-scale study of proteins in a cell or organism
Metabolomics
analysis of small molecules in a system
Transcriptomics
study of all RNA transcripts produced by the genome
4 categories of genomics
structural
functional
comparitive
epigenomics
Structural genomics
mapping and sequencing the genome
Functional genomics
understanding gene function and expression
Comparative genomics
comparing genomes across species
Epigenomics
study of heritable changes beyond DNA sequence
Metagenomics
total gene content of microbial community
Metagenomics analyzes
pooled DNA or RNA from environmental sample containing organisms which have not been isolated/identified
DNA Sequencing Methods
sanger sequencing
next-gen sequencing (NGS/illumina)
nanopore sequencing
PacBio SMRT sequencing
Sanger sequencing
chain termination
gold standard for single-gene analysis
Next-Gen Sequencing (NGS/Illumina)
massively parallel
high throughput
short reads (about 150bp)
Nanopore sequencing
real-time
long reads (>100kb)
portable MinION device
PacBio SMRT Sequencing
single-molecule real-time
long reads
low error with CCS
Sanger sequencing step 1: dsDNA fragment is
denatured into two ssDNA fragments
Sanger sequencing step 2: a fragment of
ssDNA is multiplied into millions of copies
Sanger sequencing step 3: a primer that
corresponds to one end of the fragment is attached
Sanger sequencing step 4: the fragments are
added to four polymerase solutions
Sanger sequencing step 4: each solution contains
four types of bases (dNTP) but only one type of termination nucleotide (ddNTP)
Sanger sequencing step 5: the chain grows until
a ddNTP is randomly added and when this is added DNA synthesis stops