Final answer:
Exome and genome sequencing play pivotal roles in elucidating pedigrees within genetic studies by providing comprehensive insights into the entire genetic makeup of individuals.
Step-by-step explanation:
Because exome and genome sequencing offer full insights into an individual's entire genetic makeup, they are essential tools for deciphering pedigrees in genetic investigations.
Exome sequencing identifies changes that contribute to phenotypic features by focusing on protein-coding areas. Understanding familial inheritance patterns requires the ability to identify pathogenic mutations or variants, which this technique helps with.
A more comprehensive view is provided by genome sequencing, which reveals structural differences and non-coding areas throughout the whole DNA sequence.
These methods help to clarify complicated family dynamics, find carriers of hereditary diseases, and understand how features are passed down through the generations.
your question is incomplete, most probably the complete question is:
"How can exome and genome sequencing be employed to enhance the clarification of pedigrees in genetic studies?"