L2 Genomics Flashcards

1
Q

Tree of life based on rRNA genes

A

Assert that all living things have a common ancestor

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2
Q

Organelle Genomes

A

Eukaryotic cells contain a nuclear genome and organelle/plastid genomes

multiple “genomes” exist within a eukaryotic cell

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3
Q

Eukaryotes vs Prokaryotes

A

See OneNote

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4
Q

Size and structure of organelle DNA

A
  • circular genomes

- genes for rRNA, tRNA, some proteins

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5
Q

Origin of Eukaryotic cell

A

See OneNote

Endosymbiont Hypothesis

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6
Q

rRNA comparisons - if endosymbiont

A

See OneNote

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7
Q

rRNA comparison - if endogenous

A

See OneNote

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8
Q

Comparative Genomics

A

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
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9
Q

Human vs Mouse

A

See OneNote

- there is an excess of rearrangements in rodent lineages

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10
Q

Karyotopic Evolution

A

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

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11
Q

Metagenomic

A

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

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12
Q

Phylogenomics

A

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

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13
Q

Evolutionary genomics applications

A
  • metagenomics
  • phylogenomics
  • non-model => new-model organisms
  • functional genomics
  • population genomics
  • trait mapping
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14
Q

Dideoxy Sequencing

A

See OneNote

- Fred Sanger

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15
Q

The first sequencing of the human genome

A

See OneNote

  • dideoxy sequencing
    1. automated calling with dyes
    2. high-resolution traces
    3. Solexa’s: reversible terminator chemistry
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16
Q

Solexa

A

See OneNote Solexa page

17
Q

Barcodes

A

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

18
Q

Indexing

A

To distinguish between the clusters and thereby allow correct paired end assignments

19
Q

Paired end

A

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.

20
Q

Mate pairs

A

See OneNote note and mate pair page

21
Q

Pyrosequencing

A

See OneNote page on Pyrosequencing

Sequencing by synthesis

22
Q

PacBio

A

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

23
Q

Nanopore sequencing

A

Sequencing can be done with a very small machine, able to take out into the environment