L2 Genomics Flashcards
Tree of life based on rRNA genes
Assert that all living things have a common ancestor
Organelle Genomes
Eukaryotic cells contain a nuclear genome and organelle/plastid genomes
multiple “genomes” exist within a eukaryotic cell
Eukaryotes vs Prokaryotes
See OneNote
Size and structure of organelle DNA
- circular genomes
- genes for rRNA, tRNA, some proteins
Origin of Eukaryotic cell
See OneNote
Endosymbiont Hypothesis
rRNA comparisons - if endosymbiont
See OneNote
rRNA comparison - if endogenous
See OneNote
Comparative Genomics
study of the pattern of similarity and difference between genomes of different species
central concept:
- sequence homology, identity because it derived from a common ancestor
- infer process from pattern
Human vs Mouse
See OneNote
- there is an excess of rearrangements in rodent lineages
Karyotopic Evolution
See OneNoten diagram
- chromosome number changes e.g. chimps have one more chromosome than humans
Short repeats = telomeres
Telomere in the middle of the chromosome arm indicates that the telomere there was once active
Metagenomic
Metagenomics is the study of genetic material recovered directly from environmental samples. The broad field may also be referred to as environmental genomics, ecogenomics or community genomics.
Can now sample genomes that are not culturable in the lab
Phylogenomics
Phylogenomics is the intersection of the fields of evolution and genomics. The term has been used in multiple ways to refer to analysis that involves genome data and evolutionary reconstructions. It is a group of techniques within the larger fields of phylogenetics and genomics.
How organisms are related to each other at the genomic level
Evolutionary genomics applications
- metagenomics
- phylogenomics
- non-model => new-model organisms
- functional genomics
- population genomics
- trait mapping
Dideoxy Sequencing
See OneNote
- Fred Sanger
The first sequencing of the human genome
See OneNote
- dideoxy sequencing
1. automated calling with dyes
2. high-resolution traces
3. Solexa’s: reversible terminator chemistry
Solexa
See OneNote Solexa page
Barcodes
DNA barcoding is a taxonomic method that uses a short genetic marker in an organism’s DNA to identify it as belonging to a particular species.[1] It differs from molecular phylogeny in that the main goal is not to determine patterns of relationship but to identify an unknown sample in terms of a preexisting classification.[2] Although barcodes are sometimes used in an effort to identify unknown species or assess whether species should be combined or separated
Indexing
To distinguish between the clusters and thereby allow correct paired end assignments
Paired end
See OneNote paired end page
Paired-end sequencing allows users to sequence both ends of a fragment and generate high-quality, alignable sequence data. Paired-end sequencing facilitates detection of genomic rearrangements and repetitive sequence elements, as well as gene fusions and novel transcripts.
Mate pairs
See OneNote note and mate pair page
Pyrosequencing
See OneNote page on Pyrosequencing
Sequencing by synthesis
PacBio
Their custom dyes join not to the nucleotide but to the phosphate so the reaction works much more frequently as you don’t need to deblock, can get very long reads
Nanopore sequencing
Sequencing can be done with a very small machine, able to take out into the environment