Types of SNPS: Select one: a. • Non-coding region. O b. Causative SNPS. • All of above answer. O d. • Coding region Clear my choice

Q: What is the correct order of the gene sequence given the following information: BD - 14% CD - 12% AD…

A: BASIC INFORMATION ABOUT GENETIC MATERIAL  DNA It stands for deoxyribo nucleic acid.  It is the…

Q: A next-generation method of DNA sequencing, 454 sequencing, uses pyrosequencing in which the…

A: Pyrosequencing is a next-generation technique of DNA sequencing. This method can be used to detect…

Q: Indicate 2 differences between SSLP (simple sequence length polymorphism) and SNP (single nucleotide…

A: SSLPs are called Simple Sequence Length Polymorphism. These are arrays of repeat sequences that…

Q: Mapping is the bioinformatics term used to describe alignment of sequence reads to a reference…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: An effective DNA probe can sometimes be developed by knowing the amino acid sequence of the protein…

A: A segment of DNA to be cloned is known as probe. It could be radioactive in gel electrophoresis

Q: You are a public health official trying to determine the identity of the pathogen circulating within…

A: Answer :- Improvements made in the DNA sequencing innovation prompts the total investigation of…

Q: The BLAST program is a tool fora. inserting many DNA fragments into a cell at the same time.b.…

A: With the formation of molecular biology as a branch of science, scientist began to work on the…

Q: Why are the first 20 bases typically ignored from a Sanger sequencing .ab1 file? The data quality is…

A: The data quality is too low and the data is noisy

Q: Explain in your own words what a SNP is.

A: DNA is the genetic material in almost all organisms. It is formed by four nucleotides A,T,G,C.

Q: When we need to perform Southern, Western and Northern blotting? How they are different from one…

A: Blotting is the technique used to transfer the DNA, RNA, or protein sequence on a carrier membrane…

Q: Which of the following is a transversion mutation Select 4 correct answer(s) OA --> T OC--> T C -->…

A: Point mutations The mutations that occur at single base nucleotides are called a base or point…

Q: The photo where there is written "procedure" is the procedure, while the other photo where there is…

A: Linked Genes ---Introduction and Hypothesis --Answer ( a ) When genes are on separate chromosome or…

Q: Which of the following process generates a new copy of the transposable element at a new location of…

A: Transposition is a DNA recombination reaction that results in the translocation of a discrete DNA…

Q: Which statement is right the polyclonal antibody is expensive to produce the monoclonal antibody…

A: Antibodies are giant Y-shaped proteins known as immunoglobulins that are created by B cells as a…

Q: A collection of recombinant vectors that carry fragments of chromosomalDNA is calleda. a genomic…

A: Recombinant vectors are generally some live replicating virus particles which carry some extra genes…

Q: ESTs are ________. a. generated after a cDNA library is made b. unique sequences in the genome c.…

A: The composition of inheritable information in an organism is its genome. Each organism has a…

Q: In class, we discussed Down syndrome and its cause. Which lab techniques allows us to diagnose…

A: Down syndrome is a genetic disorder that is caused by the presence of an extra chromosome no. 21  It…

Q: Which of the following will lead to DNA cutting more frequently? Choose all that apply.

A: The restriction enzymes are enzymes that cut the DNA at specific nucleotide sequences called the…

Q: Why are the first 20 bases typically ignored from a Sanger sequencing ab1 file? O The data quality…

A: The most commonly used tool for detecting SNVs is Sanger sequencing, it involves DNA polymerase…

Q: If companies like 23 and me should be allowed to sequence your DNA and give you the results instead…

A: 23andMe is a privately held personal genomics and biotechnology company based in Sunnyvale,…

Q: You can introduce precise edits into the genome using Crispr/Cas9 and , O A. ligation O B. homology…

A: Genome editing  It is a technology use by scientists to change the sequence of perticular part of…

Q: What would be a medical advantage of having a catalog of SNPs?

A: A single-nucleotide polymorphism is a substitution of a single nucleotide at a unique position in…

Q: An elderly woman took a prescription medicine to help her to sleep; however, she felt restless all…

A: Sleeping tablets are prescribed to treat insomnia. They fall under the category of…

Q: The BLAST program begins with a particular genetic sequence anda. translates it into an amino acid…

A: Homologous genes have similar DNA sequences which emphasizes that the proteins encoded by these…

Q: A. In practice, U.S. [ Select ] ["eugenics", "gene therapy", "recombinant DNA", "population…

A: The human body is a well built machine in which all the organs coordinate together to make it work.…

Q: Comparing SNPs to STR markers, which of the following are true? Select one: a. SNP loci generally…

A: Question: Comparing SNPs to STR markers, which of the following are true?

Q: Your Southern blot shows no results, everything is blank.Give two possible explanations for what may…

A: Southern blotting is the most common molecular biology technique. A Southern blot is defined as a…

Q: Which of the following methods use(s) a labeled nucleic acidprobe, such as a labeled fragment of…

A: DNA is the genetic material that carries genetic information in the form of coded nucleotide…

Q: The CRISPR system may be used to manipulate the genome in human cells, because Cas9 can

A: CRISPER system can use Cas protein to manipulate the genome present in human cell.

Q: An RFLP marker is located 1 million bp away from a gene of interest. Your goal is to start at this…

A: Molecular mapping is used to find the location of gene on the chromosome and also the distance…

Q: DNA polymorphisms can be used as DNA markers. Describe the differences between SNPs and STR…

A: DNA markers can help link an inherited disease with the responsible gene. the most common types of…

Q: An individual’s unique set of_______ can be used in DNA profiling. a. DNA sequences c. SNPs b. short…

A: Introduction  In the genome, there is usually two types of nucleic acid sequence present. One is…

Q: Types of SNPS: Select one: О . Causative SNPS. O b. • All of aboove answer. Non-coding region.…

A: SNP called the single nucleotide polymorphism helps to find out a gene that is causing disease.

Q: Finding and developing of a biomarker is very difficult because of the uniqueness of the individual…

A: Answer: BIOMARKERS : These are the biological molecules which are used to measure and monitor the…

Q: A transversion mutation would be replacing T by:   a. C   b. T   c. either A or G   d. U

A: Transversion mutation is a type of substitution mutation. A gene mutation that results from the…

Q: A.) Homologous recombination repair are prone to error and can cause loss of genome integrity.…

A: DNA repair guarantees an organism' existence by allowing children to acquire parental DNA as…

Q: ations.

A: SNPs is single nucleotide polymorphism ,these are positions in genome where some individuals have…

Q: Select all that apply: A SNP (single nucleotide polymorphism) is similar to an STR (short tandem…

A: SNP and STR loci are explored for human identity testing projects, mitochondrial DNA testing, and…

Q: Give the information about DNA mutation types from SNP to large structural variation.

A: Hugo de Vries was the first one to coin the term “mutation.” It is studied under the domain of…

Q: Which of the following mutagens results in the deamination of nitrogenous bases? O nitrous acid base…

A: The amino bases adenine and cytosine lose one amino group when they are oxidised. As a result, in…

Q: What type of mutations are the most harmful to an organism? Select at least 2 answers Duplication…

A: A mutation is a permanent change in the DNA of a cell such that the sequence deviates from what is…

Q: Genomics can be used on a personal level to: a. decrease transplant rejection b. predict genetic…

A: Genomics is a branch of biology that deals with the entire genes and their interactions with each…

Q: describe one example of an SNP that resulted in

A: A SNP could be a variation of one nucleotide between people

Q: The best molecular technique to quantify the gene transcripts is (write in fu!!).

A: The Central Dogma concept states that "DNA makes RNA and RNA makes protein". This concept is…

Q: To achieve a 10x depth coverage for a genome of length 10 Mbp, how many reads of 100 bp are…

A: A Coverage is multiplier based on  total size of the genome. Formula =  Coverage = (read length) x…

Q: Briefly explain how Genome Wide Association Studies (GWAS) are done. Then, using this example of a…

A: A genome-wide association study (GWAS) is a methodology utilized in hereditary qualities examination…

Q: conditional mutation when there is an alteration to the coding region of a gene is caused by A.…

A: Changes in nucleotides in DNA may cause mutations.  This my alter DNA sequence of a gene or make…

Q: Can you list 10 recombinant proteins which are used in medical practice? Find out where they are…

A: Recombinant protein is a modified form of protein, which is produced to obtain more desirable…

Q: Match each type of variant with the best technique that could be used to detect the variant. (Hint:…

A:

Genomic studies

Genomic studies (genomics) is the study of the whole genome of an organism. Using bioinformatics and high-performance computing, genomic researchers examined massive amounts of deoxyribonucleic acid (DNA)-sequence data to discover variations or mutations that affect drug response, health, or disease. Genomics is a much younger discipline than genetics, having only emerged in the last few decades as a result of technological advancements in DNA sequencing and computational biology.