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Bioc4010 Sample Questions:

1. A) What is the base call accuracy of a base in an Illumina sequenced short
read with a Q value of 20?
B) Is this better or worse than a Q value of 10?

Answer: A) Probability 1 in 100 or 99% call accuracy
B)Better. Q10 corresponds to a probability of 1 in 10 or 90% call accuracy


Formula: Q = -10 log10 P


2. What two primary advantages does exome sequencing provide over whole
genome sequencing?

Answer: Cost and data reduction. Exome capture limits the sequencing to known
protein-coding genes and some miRNAs.


3. Split and sort the string ‘CAPTAINKIRK’ into its appropriate suffix array

Answer:

Ainkirk
Aptainkirk
Captainkirk
Inkirk
Irk
K
Kirk
Nkirk
Ptainkirk
Rk
Tainkirk
4. Given a base-quality score threshold of Q30, the following short read
alignment, and reference sequence, what is the genotype (two alleles, eg
G/C)at the indicated position? Base qualities for the position are listed on the
side for each of the reads.




AGCTCCCAGGGTCCAG                                   Q29
          GTCCAGTCTCGGTT                           Q40
      CAGGGTCCAGTC                                 Q47
           TCCAGTCTCGGTTCCATC                      Q35
    CCCAGGGCCCAG                                   Q50
        GGGTCCAGTCTC                               Q31
   TCCCAGGGCC                                      Q10
       AGGGTCCAGT                                  Q45
 GCTCCCAGGGCCCAGTCT                                Q46
CTCCCAGGGCCC                                     Q33
CCAGGGTCCAGTCQ38
 GCTCCCAGGGCCCAGTCTCGG                              Q41
      CAGGGTCCAGTCTCG                               Q15
AGCTCCCAGGGTCCAGTCTCGGTTCCATCTA
           *

Answer: Discard the reads where the base quality score is below Q30. Sum up the
reference and alternate bases at the position. (T =6 , C = 4). Therefore the genotype
called is T/C (heterozygous).


5. Sort the following types of genetic variants into the categories: Potentially
Disease Causing, Unlikely to be Disease Causing

1. Splice Site
2. Non-Synonymous
3. Synonymous
4. FrameshiftIndel
5. Stop Loss
6. Stop Gain
7. Intronic (Non-Splice Site)
8. Intergenic


Answer:

Disease: 1, 2, 4, 5, 6
Non-Disease: 3, 7, 8
6) What is the primary motivation for using “next gen” sequencing methods
and modern genomics approaches to diagnosing human genetic diseases?

Answer: Cost

7) What does the base quality of a sequencing read tell you?

Answer: The base quality is equivalent to the probability of an incorrect base call.
(Also acceptable answer is the base call accuracy)

8) What problem does binary search address?

Answer: Efficiently searching the index of a genome

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Bioc4010 sample questions

  • 1. Bioc4010 Sample Questions: 1. A) What is the base call accuracy of a base in an Illumina sequenced short read with a Q value of 20? B) Is this better or worse than a Q value of 10? Answer: A) Probability 1 in 100 or 99% call accuracy B)Better. Q10 corresponds to a probability of 1 in 10 or 90% call accuracy Formula: Q = -10 log10 P 2. What two primary advantages does exome sequencing provide over whole genome sequencing? Answer: Cost and data reduction. Exome capture limits the sequencing to known protein-coding genes and some miRNAs. 3. Split and sort the string ‘CAPTAINKIRK’ into its appropriate suffix array Answer: Ainkirk Aptainkirk Captainkirk Inkirk Irk K Kirk Nkirk Ptainkirk Rk Tainkirk
  • 2. 4. Given a base-quality score threshold of Q30, the following short read alignment, and reference sequence, what is the genotype (two alleles, eg G/C)at the indicated position? Base qualities for the position are listed on the side for each of the reads. AGCTCCCAGGGTCCAG Q29 GTCCAGTCTCGGTT Q40 CAGGGTCCAGTC Q47 TCCAGTCTCGGTTCCATC Q35 CCCAGGGCCCAG Q50 GGGTCCAGTCTC Q31 TCCCAGGGCC Q10 AGGGTCCAGT Q45 GCTCCCAGGGCCCAGTCT Q46 CTCCCAGGGCCC Q33 CCAGGGTCCAGTCQ38 GCTCCCAGGGCCCAGTCTCGG Q41 CAGGGTCCAGTCTCG Q15 AGCTCCCAGGGTCCAGTCTCGGTTCCATCTA * Answer: Discard the reads where the base quality score is below Q30. Sum up the reference and alternate bases at the position. (T =6 , C = 4). Therefore the genotype called is T/C (heterozygous). 5. Sort the following types of genetic variants into the categories: Potentially Disease Causing, Unlikely to be Disease Causing 1. Splice Site 2. Non-Synonymous 3. Synonymous 4. FrameshiftIndel 5. Stop Loss 6. Stop Gain 7. Intronic (Non-Splice Site) 8. Intergenic Answer: Disease: 1, 2, 4, 5, 6 Non-Disease: 3, 7, 8
  • 3. 6) What is the primary motivation for using “next gen” sequencing methods and modern genomics approaches to diagnosing human genetic diseases? Answer: Cost 7) What does the base quality of a sequencing read tell you? Answer: The base quality is equivalent to the probability of an incorrect base call. (Also acceptable answer is the base call accuracy) 8) What problem does binary search address? Answer: Efficiently searching the index of a genome