7. Given below are some terms in Column A and their corresponding properties/related terms in column B Which one of the following options represents the most appropriate match between all terms of column A and B (1) A-(ii), B-(iv), C-(i), D-(iii) (2) A-(iii), B-(i), C-(iv), D-(ii) (3) A-(iv),B-(iii), C-(iv), D-(i) (4) A-(iii), B-(iv), C-(i), D-(ii)
  1. Given below are some terms in Column A and their corresponding properties/related terms in column B

    Which one of the following options represents the most appropriate match between all terms of column A and B
    (1) A-(ii), B-(iv), C-(i), D-(iii)
    (2) A-(iii), B-(i), C-(iv), D-(ii)
    (3) A-(iv),B-(iii), C-(iv), D-(i)
    (4) A-(iii), B-(iv), C-(i), D-(ii)

    Column A vs Column B

    Column A:
    A. Bulk segregant analysis
    B. NILs (Near isogenic lines)
    C. Association mapping
    D. SNPs

    Column B:
    (i) QTL analysis of wider genetic diversity using fewer individuals
    (ii) Mapping monogenic qualitative traits
    (iii) Co-dominant markers
    (iv) Repeated backcrossing of F1 to recurrent parent

    Correct matches:

    • A → (i)

    • B → (iv)

    • C → (ii)

    • D → (iii)

    So the full pattern is A–iv, B–iii, C–ii, D–i in option notation.


    Why each match is correct

    • A. Bulk segregant analysis → (i) QTL analysis of wider genetic diversity using fewer individuals

      • BSA pools DNA from individuals with extreme phenotypes and compares marker frequencies between bulks, allowing QTL detection using relatively few individuals.​

    • B. NILs → (iv) Repeated backcrossing of F1 to recurrent parent

      • Near isogenic lines are created by repeatedly backcrossing F1 and later generations to a recurrent parent, selecting for a donor segment each generation.​

    • C. Association mapping → (ii) Mapping monogenic qualitative traits

      • Association (linkage disequilibrium) mapping is well suited to detect loci controlling qualitative traits based on marker–trait associations in diverse germplasm.​

    • D. SNPs → (iii) Co-dominant markers

      • Single nucleotide polymorphisms are codominant markers, as heterozygotes can be distinguished from both homozygotes by genotyping.​

    Thus the option that lists these correctly is:

    • (3) A–iv, B–iii, C–ii, D–i.

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