If you worked backward, starting with the amino acid sequence of the protein, would you obtain the same DNA nucleotide sequence?  Why or why not?

What is a DNA library? Do you think this name is appropriate?

Discuss the experiments Griffith, Avery and Hershey/Chase did in the early 1920-50s that helped determine DNA was the genetic stuff.  What was the “take home” from each?

On the image below what is the next nucleotide to be added on the oldest Okazaki fragment (use picture)? A C G T

The goal of many computer programs is to identify sequence elementswithin a long segment of DNA. What is a sequence element? Givetwo examples. How is the specific sequence of a sequence elementdetermined? In other words, is it determined by the computer programor by genetic studies? Explain.

Where do you expect to see multiple “Ns” within a sequencing read? a)Within the first 25 nucleotides from the beginning of the sequence and from the last 25 nucleotides of the sequence.   b)In the middle of the sequence and from the last 25 nucleotides of the sequence. d   c)From the last 25 nucleotides of the sequence.   d)Within the first 25 nucleotides from the beginning of the sequence.   e)In the middle of the sequence.

What is the symbol on the first line of a raw read that tells you a unique sequence follows?

The following question is related to Restriction Enzymes and RFLP. Using EcoRl, the smallest fragments between DNA sequence A and B were how many base pairs?

The bases are linked to the _ position of the 5 carbon sugar in a nucleotide Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a a) 1' b) 2' с) 3' d d) none of the above

What did Rosalind Franklin do when she saw Watson and Crick’s first model? Why?