Family Markers: Using Multiply-Affected Families to Identify Risk Genes
What does the DAO gene do?
How did researchers identify DAO and other possible genes linked to bipolar disorder?
You might see a message like Warning: kinship2 package is deprecated for R <= 4.5; switch functionality to Pedixplorer from BioConductor. This is not a problem, and you can still proceed!
Why might we want to install add-on packages in R?
How can we confirm that our data loaded correctly? Take a screenshot and point to your evidence.
Looking at the description and contents of the
bipolaranddepressioncolumns, what do you think the columndiagnosis_availablerepresents? Take a screenshot that shows this column.
How many generations were assessed in this pedigree? Take a screenshot and label them.
How many male individuals and how many female individuals are present? Take a screenshot and label them.
What is the diagnosis for individual 9? Individual 10? Take a screenshot and circle these individuals.
What is the diagnosis for individual 12? Take a screenshot and circle this individual.
We already know that DAO is the gene of interest. Why is DAO a better match than IL6 for the diagnosis (based on the pedigree)?
How many copies of the DAO variant do you think are necessary to cause bipolar disorder?
Many individuals are missing diagnoses, genotypes, or both. Why do you think that might be the case?
What could be done to add more certainty to our conclusions? More genotyping, more diagnostics, or more genes collected?