Midterm (Version A) Solutions Fall 2011
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University
Toronto Metropolitan University (TMU)
Course
BME 501: Bioinformatics
Format
Midterm Exam
Year
2011
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BME501/CPS501 Midterm Version A, Nov 4, 2011. Ryerson University
1. (2 marks) You are the finisher and you need to arrange these 8 sequenced
segments of DNA to build the largest possible contigs with the minimum number of
gaps. Assume that an overlap of 5 bases is significant. Draw the contigs showing
the overlapping segments.
GGCGTCGGCGAGATCATCTGTGACAATC
GAAGGTACCTCAAGGTATTG
GAGTGTGTCGTCGTTGGCGT
GTATGAGGAGAGTATGAGTG
ATCTGTGACAATCCATCTTG
GAGTGTGTCGT
GGCGTCGGCGAGATCATCTG
TATTGTATAATCCCCATCCC
GGCGTCGGCGAGATCATCTGTGACAATC
GAGTGTGTCGTCGTTGGCGT ATCTGTGACAATCCATCTTG
GTATGAGGAGAGTATGAGTG GGCGTCGGCGAGATCATCTG
GAGTGTGTCGT
TATTGTATAATCCCCATCCC
GAAGGTACCTCAAGGTATTG
2. (2 marks) Assume that (1) a primer for PCR is 5 bases long, and (2) that the
contigs you generated in question 1 are close enough in the genome that you can
use PCR to make fragment(s) that will close gaps, and (3) that the contigs line up
longest to shortest going left to right in the genome. What are the sequences of the
primers that you would use?
We want to generate a fragment that looks like TCTTG.............GAAGG, so that we can link
up the two contigs. The left primer therefore would be TCTTG, and the right primer would
be the reverse complement of GAAGG, so CCTTC.
3. (1 mark) Provide evidence (other than BLAST) regarding whether the first sequence
in Question 1 is βcodingβ.
Putting the first sequence GGCGTCGGCGAGATCATCTGTGACAATC into Testcode program on
geneticsplace, we get the result 1.199 β probably coding.
4. (3 marks) (a) What is the GC content of the first fragment (sequence) in question
1? (b) What is the GC skew? (c) Would either of these values be different if you did
the calculation on the complementary strand? Explain and show your work for each
answer. (You can use an online application to confirm your answer, but you must
show a manual calculation.)
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