342823
The credit for developing a method for determination of nucleotide sequence in DNA as well as amino acid sequence in protein goes to:
1 Frederick Taylor
2 James Sanger
3 Frederick Sanger
4 Jacob Sanger
Explanation:
The fragments were sequenced using automated DNA sequencers that worked on the principle of a method developed by Frederick Sanger. (Remember, Sanger is also credited for developing method for determination of amino acid sequences in proteins).
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342824
Under HGP, scientists have, located 1.4 million locations where difference in single DNA base exists. It is termed as :
1 Minisatellite
2 Single nucleotide polymorphism
3 Microsatellites
4 Simple nucleotide polymorphism
Explanation:
Scientists have identified about 1.4 million locations where singlebase DNA differences (SNPs - single nucleotide polymorphism, pronounced as 'snips') occur in humans.
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342825
Repetitive DNA make up very large portion of human genome and are important for studying
1 Chromosome structure
2 Chromosome dynamics, Evolution
3 Both 1 & 2
4 None of these
Explanation:
Repetitive sequences are stretches of DNA sequences that are repeated many times, sometimes hundred to thousand times. They are thought to have no direct coding functions, but they shed light on chromosome structure, dynamics and evolution
342823
The credit for developing a method for determination of nucleotide sequence in DNA as well as amino acid sequence in protein goes to:
1 Frederick Taylor
2 James Sanger
3 Frederick Sanger
4 Jacob Sanger
Explanation:
The fragments were sequenced using automated DNA sequencers that worked on the principle of a method developed by Frederick Sanger. (Remember, Sanger is also credited for developing method for determination of amino acid sequences in proteins).
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342824
Under HGP, scientists have, located 1.4 million locations where difference in single DNA base exists. It is termed as :
1 Minisatellite
2 Single nucleotide polymorphism
3 Microsatellites
4 Simple nucleotide polymorphism
Explanation:
Scientists have identified about 1.4 million locations where singlebase DNA differences (SNPs - single nucleotide polymorphism, pronounced as 'snips') occur in humans.
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342825
Repetitive DNA make up very large portion of human genome and are important for studying
1 Chromosome structure
2 Chromosome dynamics, Evolution
3 Both 1 & 2
4 None of these
Explanation:
Repetitive sequences are stretches of DNA sequences that are repeated many times, sometimes hundred to thousand times. They are thought to have no direct coding functions, but they shed light on chromosome structure, dynamics and evolution
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BIOXII06: MOLECULAR BASIS OF INHERITANCE
342823
The credit for developing a method for determination of nucleotide sequence in DNA as well as amino acid sequence in protein goes to:
1 Frederick Taylor
2 James Sanger
3 Frederick Sanger
4 Jacob Sanger
Explanation:
The fragments were sequenced using automated DNA sequencers that worked on the principle of a method developed by Frederick Sanger. (Remember, Sanger is also credited for developing method for determination of amino acid sequences in proteins).
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342824
Under HGP, scientists have, located 1.4 million locations where difference in single DNA base exists. It is termed as :
1 Minisatellite
2 Single nucleotide polymorphism
3 Microsatellites
4 Simple nucleotide polymorphism
Explanation:
Scientists have identified about 1.4 million locations where singlebase DNA differences (SNPs - single nucleotide polymorphism, pronounced as 'snips') occur in humans.
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342825
Repetitive DNA make up very large portion of human genome and are important for studying
1 Chromosome structure
2 Chromosome dynamics, Evolution
3 Both 1 & 2
4 None of these
Explanation:
Repetitive sequences are stretches of DNA sequences that are repeated many times, sometimes hundred to thousand times. They are thought to have no direct coding functions, but they shed light on chromosome structure, dynamics and evolution
342823
The credit for developing a method for determination of nucleotide sequence in DNA as well as amino acid sequence in protein goes to:
1 Frederick Taylor
2 James Sanger
3 Frederick Sanger
4 Jacob Sanger
Explanation:
The fragments were sequenced using automated DNA sequencers that worked on the principle of a method developed by Frederick Sanger. (Remember, Sanger is also credited for developing method for determination of amino acid sequences in proteins).
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342824
Under HGP, scientists have, located 1.4 million locations where difference in single DNA base exists. It is termed as :
1 Minisatellite
2 Single nucleotide polymorphism
3 Microsatellites
4 Simple nucleotide polymorphism
Explanation:
Scientists have identified about 1.4 million locations where singlebase DNA differences (SNPs - single nucleotide polymorphism, pronounced as 'snips') occur in humans.
BIOXII06: MOLECULAR BASIS OF INHERITANCE
342825
Repetitive DNA make up very large portion of human genome and are important for studying
1 Chromosome structure
2 Chromosome dynamics, Evolution
3 Both 1 & 2
4 None of these
Explanation:
Repetitive sequences are stretches of DNA sequences that are repeated many times, sometimes hundred to thousand times. They are thought to have no direct coding functions, but they shed light on chromosome structure, dynamics and evolution