Databases & tools, comparative genomics I

23 important questions on Databases & tools, comparative genomics I

Where are sequences stored?

In sequence databases

Where are all databases crosslinked?

At NCBI

What are examples of genome browsers?

  • Ensembl
  • UCSC
  • NCBI Genome Data Viewer
  • RefSeq collection
  • Higher grades + faster learning
  • Never study anything twice
  • 100% sure, 100% understanding
Discover Study Smart

What are 4 sequence analysis tools?

  • ORF mapping
  • Secondary structure prediction
  • Pattern recognition
  • Sequence alignment

What is a method for secondary structure prediction?

The Chou-Fasman method

What is sequence alignment?

Finding the biological relevance of a certain sequence (similar sequences suggest similar function, evolutionary history)

What tool can you use for sequence alignment?

Basic Local Aligment Search Tool (BLAST)

What are the different BLAST algorithms?

  • BLASTP: protein - protein
  • BLASTN: DNA - DNA
  • BLASTX: translated DNA - protein
  • TBLASTN: protein - translated DNA
  • TBLASTX: translated DNA - translated DNA

What is comparative genomics based on?

- On the idea that similarities in DNA suggest homology and evolutionary relatedness,
- and that differences in DNA suggest differences in function and behaviour between cells, tissues and organisms.

What are examples of things that are studied in comparative genomics?

  • Ape vs. human being
  • Cancer cell vs. normal cell

What is a phylogenetic tree?

A diagram that describes the phylogeny of species.

What does the molecular clock describe?

The relatively constant rate of neutral mutations

How can the molecular clock be calibrated?

- By comparing molecular information (how related certain genes are)
- with other information on common ancestry (for example, fossil records)

How can cladograms be constructed?

Based on molecular data, such as a DNA sequence (you compare DNA sequences and you construct possible cladograms, the one with the fewest mutations necessary is the most likely one)

What are two things that you assume when using the principles of parsimony?

  • The neutral change rate is constant
  • Neutral changes are most likely in the 3rd base of the codon

Why did Carl Woese analyse rRNA for constructing cladograms?

  • The sequence has changed slowly because of the importance of the transcript
  • Fairly large molecule, so a lot of space for change

Why did Carl Woese's tree need to be revised?

Because of horizontal gene transfer, which he hadn't included in his tree.

What do you assume when you use the method of homology transfer?

That sequence similarity reflects functional similarity (which you can use when you have a protein with an unknown function)

What is the C-value paradox?

The genome size of an organism does not correlate with the gene number of the organism (humans have an average of 100,000 bases per gene, but E.coli has an average of 1,400 bases per gene)

How can genomes evolve?

  • By sequence modification: mutations (SNPs)
  • By genome structure modification:
    • deletion
    • duplication
    • translocation
    • inversion

What can be concluded when genomes of different organisms are compared with each other?

The larger the evolutionary distance, the smaller the fragments (similar to human genome) are

What happens with groups of genes with a similar function or that are involved in the same process in evolution?

They tend to remain localized in the same cluster.

Where can you find synteny between proteins?

In the Ensembl Genome Browser

The question on the page originate from the summary of the following study material:

  • A unique study and practice tool
  • Never study anything twice again
  • Get the grades you hope for
  • 100% sure, 100% understanding
Remember faster, study better. Scientifically proven.
Trustpilot Logo