Your TASK is to GROUP the terms in the table below into TWO CATEGORIES titled GENETICALLY IDENTICAL and GENETIC VARIETY. Please provide a 1–2 sentence rationale for the terms you placed in each category. Recombinant DNA Technology Cloning Selective Breeding (gene splicing) Mitosis Meiosis Twins Sexual Reproduction Fertilization Asexual Reproduction Mutations

Your TASK is to GROUP the terms in the table below into TWO CATEGORIES titled GENETICALLY IDENTICAL and GENETIC VARIETY. Please provide a 1–2 sentence rationale for the terms you placed in each category. Recombinant DNA Technology Cloning Selective Breeding (gene splicing) Mitosis Meiosis Twins Sexual Reproduction Fertilization Asexual Reproduction Mutations

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter6: Cytogenetics: Karyotypes And Chromosome Aberrations

Section: Chapter Questions

Problem 2CS: Genetics in Practice case studies are critical-thinking exercises that allow you to apply your new...

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The Meeting Sarah stared blankly at the blue paisley wallpaper. Her husband Mike sat by her side, bending and unbending a small paper clip. “Sarah and Michael, it’s good to meet you,” welcomed the genetic counselor, as she entered the room. “I apologize for being late, but I was just meeting with another couple. Let’s see, you’d like to have a child, but you’re concerned because of your family history of cystic fibrosis.” “Yes,” Sarah replied softly. “Mike and I met at a CF support group meeting a few years ago. He had a younger brother who died of cystic fibrosis, and I had a younger sister. We saw the painful lives they had—difficulty breathing, the constant respiratory infections. Although the treatments for CF are better now, we just don’t know if we can…” she trailed off. “I can certainly understand your concern,” the genetic counselor responded sympathetically. “That’s where I hope to help, by providing as much information and advice as I can. I’m glad that you came to see me…
how do i expand this into 1000 words The objective is to interpret the results of an RNA-Seq analysis to identify differentially expressed genes in breast cancer using figure 1. The data provided includes gene symbols, chromosome location, start and end points, strand, fold change, log2 fold change, p-value, and false discovery rate (FDR). The RNA-Seq analysis has identified several genes that are differentially expressed in breast cancer. These genes are located on various chromosomes and have varying levels of fold change, indicating the degree to which their expression levels differ between normal and cancerous cells. The gene with the highest fold change is EYA4, located on chromosome 6, with a fold change of 3604.4176. This indicates that the expression of this gene is over 3600 times higher in cancer cells compared to normal cells. The log2 fold change is 11.81555, which is a measure of the magnitude of the difference in gene expression. The p-value for this gene is extremely low…
Genetics of man 1)Determine the sex of the individual/patient based on your karyotyping results attached below. 2)Specify what kind of disorder this individual/patient may have based on your karyotyping results attached below .
ME History Bookmarks Profiles Tab Window Help ucture.com/courses/47420/quizzes/225324/take Question 3. Choose the best method (from lectures 19-21) for each of the following experiments. You want to determine the transcriptomic response to heat shock in [ Choose ] a normal cell line. You'want to measure the quantity of mRNA of your gene of interest in sepal vs petal cells. [ Choose ] You want to identify the mutation that has occurred in your gene o V [ Choose ] interest after EMS mutagenesis. CRISPR Map based sequencing or whole genome shotgun sequencing You want to know the DNA sequence of all of the genes in a Recombinant DNA genome. Restriction enzyme digest RT-PCR or qPCR You want to make large quantities of DNA of your gene of interest from a tiny amount of DNA. Sanger sequencing PCR You want to determine the differences between the proteins made Cloning in the sepal vs petal cells. Microarray or RNA-seq Proteomics Question 12
how do i expand this into 1000 words for a result section of a report The objective is to interpret the results of an RNA-Seq analysis to identify differentially expressed genes in breast cancer using figure 1. The data provided includes gene symbols, chromosome location, start and end points, strand, fold change, log2 fold change, p-value, and false discovery rate (FDR). The RNA-Seq analysis has identified several genes that are differentially expressed in breast cancer. These genes are located on various chromosomes and have varying levels of fold change, indicating the degree to which their expression levels differ between normal and cancerous cells. The gene with the highest fold change is EYA4, located on chromosome 6, with a fold change of 3604.4176. This indicates that the expression of this gene is over 3600 times higher in cancer cells compared to normal cells. The log2 fold change is 11.81555, which is a measure of the magnitude of the difference in gene expression. The…
Topic: Recombinant pharmaceuticals (for the production of insulin, human growth hormone or blood clotting factors) Question Describe the molecular genetics process using proper scientific terminology. Describe the steps that are involved. How is it performed?
Hello! I have a topic to discuss for tommorow! The question goes like this: Discuss how the genetic basis of life plays a central role in biotechnology. Further, ethical considerations aside, if DNA-based technologies became widely used, discuss how they might change the way evolution proceeds, as compared with the natural evolutionary mechanisms that have operated for the past 4 billion years.
Genetics in Practice case studies are critical-thinking exercises that allow you to apply your new knowledge of human genetics to real-life problems. Case study Michelle was a 42-year-old woman who had declined counselling and amniocentesis at 16 weeks of pregnancy but was referred for genetic counseling after an abnormal ultrasound at 20 weeks of gestation. After the ultrasound, a number of findings suggested a possible chromosome abnormality in the fetus. The ultrasound showed swelling under the skin at the back of the fetuss neck; shortness of the femur, humerus, and ear length; and underdevelopment of the middle section of the fifth finger. Michelles physician performed an amniocentesis and referred her to the genetics program. Michelle and her husband did not want genetic counseling before receiving the results of the cytogenetic analysis. This was Michelles third pregnancy; she and her husband, Mike, had a 6-year-old daughter and a 3-year-old son. At their next session, the counselor informed the couple that the results revealed trisomy 21, explored their understanding of Down syndrome, and elicited their experiences with people with disabilities. She also reviewed the clinical concerns revealed by the ultrasound and associated anomalies (mild to severe intellectual disability, cardiac defects, and kidney problems). The options available to the couple were outlined. They were provided with a booklet written for parents making choices after the prenatal diagnosis of Down syndrome. After a week of careful deliberation with their family, friends, and clergy, they elected to terminate the pregnancy. Should physicians discourage a 42-year-old woman from having children because of an increased chance of a chromosomal abnormality?
write a comprehensive, one-page position paper about your stand on the practice of stem cell therapy and genetic engineering. Consider the following guide questions in establishing your arguments: •Could the widespread use of gene therapy make society less accepting of people who are different? •Will genetic engineering permanently change our society?
Please help me answer this reviewer. Write the word TRUE if the statement is correct and if not, underline the word or statement that makes the sentence incorrect and write the correct answer on the space provided. 1. RNA is the genetic material responsible for inheritance and is passed from parent to offspring. Answer: 2. The central dogma of molecular biology is the flow of genetic information from RNA to DNA to protein. Answer: 3. Triploidy produce sterile fish. Answer: 4. Experiment of Mendel on peas is characterized as ancient biotechnology. Answer:
True or False: Write Tif the statement is true and F if it is false. 1. Mutagens are commonly in the form of toxic chemicals, and harmful radiation. _2. A mutation is a change in the base sequence of RNA 3. Mutations can occur in two different types, the body and the reproductive cells. _4. Mutations affect the reproductive cells of an organism by changing the sequence of nucleotides within a gene in a sperm or an egg cell. 5. Mutations may affect only one gene, or they may affect whole chromosomes.
Activity 1.4: Essay.Direction: Explain your answer.Today, it is easy to make transgenic plants and animals. What are some important safety and ethical issues raised by this use of recombinant DNA technology? Explain your answer.