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What will be the result if we resequence the same samples contributed to the reference genome and reassemble
reads?
Step by step
Solved in 2 steps
- If you have access to the necessary computer software, make asequence file and analyze it in the following ways: What is thetranslated sequence in all three reading frames? What is the longest open reading frame? Is the sequence homologous to any known sequences? If so, does this provide any clues about the function of the sequence?What do you understand by “Sequencing by synthesis?” What is FRED score? Give anexample.Why are closure and completeness important in genome sequencing?