How is a genome rebuilt from reads?
What comes out of a sequencing instrument?
What does more coverage do to base accuracy?
You need cheap accurate bases over simple ground. Which reads do you pick?
The same 1,000-base stretch appears in five places. A 150-base read lands inside one copy. What is the problem?
A long read can resolve a repeat by spanning it and anchoring both sides.
Circle one: True False
Unique regions assemble easily because each read has only one plausible home.
Circle one: True False
A team doubles coverage to fix a tangled repeat, but the tangle stays. What is wrong?