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NEET-UG Biology · Class 12

Human Genome Project and DNA fingerprinting — NEET & JEE Questions

Human Genome Project and DNA fingerprinting is a topic in Molecular Basis of Inheritance, a Class 12 Biology chapter of the NEET-UG syllabus. TestBudy holds 13 published NEET-UG questions on Human Genome Project and DNA fingerprinting, each with the marking scheme of the real paper. The ideas it examines include Key findings of the Human Genome Project, VNTRs and why they differ between people, Steps of DNA fingerprinting in order.

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Key formulas and concepts

The ideas Human Genome Project and DNA fingerprinting is examined on, as they are tagged in the syllabus tree.

  • Key findings of the Human Genome Project
  • VNTRs and why they differ between people
  • Steps of DNA fingerprinting in order

Human Genome Project and DNA fingerprinting MCQs with solutions

10 of the 13 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.

  1. Question 1 · difficulty L1 · recall

    A major aim of the Human Genome Project:

    • A. cloning every human
    • B. producing only recombinant insulin
    • C. eliminating mutations
    • D. determining the sequence and identifying genes in the human genome
  2. Question 2 · difficulty L1 · recall

    The highly polymorphic repeated sequences classically used in DNA fingerprinting:

    • A. telomerase proteins
    • B. histone genes only
    • C. VNTRs
    • D. ribosomal RNAs
  3. Question 3 · difficulty L2 · understanding

    What was a central goal of the Human Genome Project?

    • A. To replace all human genes with synthetic DNA
    • B. To clone every human gene into bacteria
    • C. Sequence the human genome and identify genes
    • D. To sequence only protein-coding regions
  4. Question 4 · difficulty L2 · understanding

    A major goal of the Human Genome Project was to

    • A. identify human genes and determine the nucleotide sequence of the human genome
    • B. sequence only mitochondrial DNA
    • C. eliminate all genetic variation from humans
    • D. produce identical genomes in every individual
  5. Question 5 · difficulty L2 · understanding

    DNA fingerprinting is useful because many genomic regions show

    • A. highly polymorphic sequence-length variation among individuals
    • B. exactly the same sequence in every person
    • C. no inheritance from parents
    • D. only protein-coding variation
  6. Question 6 · difficulty L3 · understanding

    Arrange the following steps of DNA fingerprinting in a correct sequence. A. Isolation of DNA and its digestion by restriction endonucleases. B. Hybridisation using a labelled VNTR probe. C. Transferring of separated DNA fragments to synthetic membranes. D. Detection of hybridised DNA fragments by autoradiography. E. Separation of DNA fragments by electrophoresis. Choose the correct answer from the options given below :

    • A. A,B,D,C,E\mathrm{A}, \mathrm{B}, \mathrm{D}, \mathrm{C}, \mathrm{E}
    • B. A,D,B,E,C\mathrm{A}, \mathrm{D}, \mathrm{B}, \mathrm{E}, \mathrm{C}
    • C. A,E,C,B,DA, E, C, B, D
    • D. A,E,B,C,D\mathrm{A}, \mathrm{E}, \mathrm{B}, \mathrm{C}, \mathrm{D}
  7. Question 7 · difficulty L3 · understanding

    DNA polymorphism forms the basis of:

    • A. Genetic mapping
    • B. DNA finger printing
    • C. Both genetic mapping and DNA finger printing
    • D. Translation
  8. Question 8 · difficulty L3 · understanding

    Transposons can be used during which one of the following?

    • A. Polymerase Chain Reaction
    • B. Gene Silencing
    • C. Autoradiography
    • D. Gene sequencing
  9. Question 9 · difficulty L3 · understanding

    DNA fingerprinting involves identifying differences in some specific regions in DNA sequence, called as

    • A. Polymorphic DNA
    • B. Satellite DNA
    • C. Repetitive DNA
    • D. Single nucleotides
  10. Question 10 · difficulty L4 · analysis

    Why are highly variable repetitive DNA regions useful in DNA fingerprinting?

    • A. They are identical in all humans
    • B. They vary among individuals
    • C. They occur only in mitochondrial DNA
    • D. They are never inherited

Common mistakes in Human Genome Project and DNA fingerprinting

Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.

  • Treats a single common marker as uniquely identifying an individual.
  • Assumes a child can possess arbitrary alleles not inherited from either parent.
  • Treats one matching marker as conclusive identification.

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