Which of the following would be of LEAST value in DNA profiling?
A) mitotyping
B) analysis of SNPs (single nucleotide polymorphisms)
C) STR (short tandem repeat) analysis
D) sequencing blood group alleles
Option D
DNA profiling is used to determine relationship between individuals on the basis of certain sequences present in their genome.
In mitotyping, mitochondrial DNA of different individuals compared. This is a particular importance because mitochondrial DNA is highly conserved between different species and between different individuals of same species.
Single nucleotide polymorphism is used to determine single changes in nucleotide of a gene.
Short tandem repeats are repetitive sequences which are present in all the individuals but their number varies.
Blood grouping will be the least valuable in DNA profiling because it is subject to change.
By determining relationships between individuals and species, we always use conserved sequences so that it is easy for us to compare the sequences and determine where the change has occurred.
Please rate.
Which of the following would be of LEAST value in DNA profiling? A) mitotyping B) analysis...
1. Answer the following questions from your knowledge on the DNA analysis and amplification lab experiment. a) What molecular mechanism is thought to operate in vivo during DNA replication with the result that dinucleotide repeats become highly polymorphic loci? b) When it comes to PCR reactions that involve a DNA target containing a dinucleotide repeat, would you expect to see any additional minor PCR products in addition to the principal product on the PAGE get? Explain your answer c) What...
Which statement about single nucleotide polymorphisms (SNPs) is true? a. SNPs can change an exon to an intron sequence. b. SNPs can change an intron sequence into an exon sequence. c. SNPs are generally responsible for frameshift mutations. d. SNPs are generally responsible for point mutations.
In 1994, Congress passed the DNA Identification Act which authorized the FBI to do 2 things: (1) create and maintain a national DNA database, and (2) establish standards for forensic DNA testing. Because the human genome is full of DNA tandem repeats and because they vary in the number of contiguous repeat units, it was decided to use tandem repeats to build the DNA database. In 1996, 13 loci were chosen to be the core short tandem repeats (STR) for...
You find a repetitive sequence with a 170 bp repeating unit in a new mammalian species. Most likely, this is a. a globin paralog. b. a LINE c. a short tandem repeat. d. a microsatellite. e. part of the centromere. A difference between a G and an A at a particular nucleotide is an example of a(n) a. SNP b. DNA transposon. c. microarray. d.microsatellite. e. STR.
1. Which of the following is / are TRUE regarding a DNA molecule? a) A SINGLE DNA molecule consists of 2 nucleotide chains b) Covalent, phosphodiester bonds connect the nucleotides of a single nucleotide chain together c) Phosphodiester bonds join the separate nucleotide chains to one another forming a single molecule d) Hydrogen bonds join the separate nucleotide chains to one another forming a single molecule 2. During DNA replication, the enzyme helicase: a) Unwinds the double helix b) Functions...
Which of the following is true regarding DNA sequencing? (multiple answers possible) a. Next generation sequencing is limited to simultaneous sequencing of 23 different nucleotide chains at a time b. Next generation sequencing or “sequencing by synthesis”, requires ddNTPs c. DNA fragments generated by the Sanger sequencing reaction each contain a primer incorporated at the 5’ end of the nucleotide chain. d. Primers are labeled with different flurophores allowing all 4 chain termination reactions for Sanger sequencing to be combined...
Next-generation sequencing involves: A. generating many short sequences from an intact, continuous DNA sequence. B. generating many short sequences from fragmented DNA. C. splicing together DNA fragments. D. adding multiple probes to fragmented DNA. What is the difference between a mutation and a polymorphism? A. A mutation can exist in a single person; a polymorphism must exist in at least 2% of the population. B. A mutation involves a single base pair; a polymorphism involves many base pairs. C. Mutations...
1) When comparing the genome of a prototypic bacterium such as E.coli, and the genome of a human, which of the following statements is true? a. The genome of E.coli is a single, circular, double stranded piece of DNA; the human genome is comprised of several linear chromosomes b. The genome size of E.coli is approximately 4.5 x 106 base pairs; the size of the human genome is approximately 3.2 x 109 base pairs c. The genome size of E.coli...
14. Restriction endonucleases are a. enzymes that restrict DNA synthesis b. enzymes that cut DNA in specific sequences c. nuclear proteins that are involved in transcription d. components of the ribosomes involved in protein synthesis 15. The first step in southern blotting is a. converting DNA into RNA b. cutting high molecular weight DNA into smaller pieces c. converting RNA into DNA d. radioactively labeling the DNA so it can be detected after the procedure is complete 16. The major...
The Sanger method of DNA sequencing uses which chain-terminating ingredient to separate fragments differing by a single nucleotide a. Magnesium b. Heat c. ddNTPs d. restriction enzymes e. none of the above