Lecture 13 Flashcards

1
Q

supermatrix

A
  • directly inferred from seq data through the construction of a large multiple seq alignment for simultaneous analysis of final data-matrix
  • often sacrifice completeness in interest of size
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2
Q

supertree

A

compile many source trees w/partially overlapping taxa into single tree; strictly topological; do not rely directly on primary data (cant go back and reanalyze with other parameters)

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3
Q

issues with supertree methods

A
  • data independence: some data can contribute to more than one souce tree
  • signal enhancement: novel relationship in supertree contradicting source trees
  • assessment of uncertainty/confidence
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4
Q

Pros of Sanger seq

A

PCR-based, dependable, easy to target specific genes, accurate

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5
Q

cons of Sanger seq

A

max ~1000 bases in single rxn, expensive, primers

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6
Q

pros of NGS

A

huge amount of seqs, cheap, do not need prior knowledge

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7
Q

cons of NGS

A

inaccurate (~99%), overkill to target particular region, short reads, seq random parts of genome

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8
Q

phylogenomics

A

integration of evolutionary reconstructions and genome seq analysis

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9
Q

metagenomics

A

1) catalogue diversity w/barcoding (OTUs)
2) true metagenome of genes present in environmental sample
- herbivores-> amino acid synthesis genes; carn-> aa degradation genes

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10
Q

Dinsdale (2008) metagenome study

A

found rel contribution of functional categories of genes differed but the total complement was similiar

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11
Q

Why is it difficult to use RAD to reconstruct a phylogeny?

A
  • more difficult to dtmn homology

- restriction sites change as spp diverge

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12
Q

reciprocal translated BLAST

A

helps find homologous genes across spp, but paralogs make things complicated

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13
Q

phylogenetic informativeness profiles

A

Townsend (2007); determine most appropriate genes for resolving particular relationships; use genes evolving slower and help avoid saturation

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14
Q

access to numerous genomes can be informative how?

A

informative marker discovery, gene order and gene loss studies, influence of organelle genomes

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15
Q

minimum optimal # of genes needed for equivalency to entire genome?

A

20

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