Problem:
Question 1: Briefly compare and contrast 454 and Illumina sequencing.
Question 2: You have prepared a metagenome, and have just received the data from the sequencing company. Describe what you would do nextwith the data.
Question 3: Using examples to illustrate your answer, what are the advantages and disadvantages of metagenome data compared to amplicon diversity data?
Could someone explain this to me?