Suppose six populations of butterflies from six different geographic locations were genetically analyzed. It was determined that each of the six populations had a different arrangement of chromosome 3. The banding pattern of the ancestral chromosome wa numbered 98765432. 9. 8. 3 2 Variant 1 Variant 2 Variant 3 Variant 4 Variant 5 98755432 97855432 85549732 853549732 53549732 Order A Order B 53549732 853549732 85549732 97855432 98755432 97855432 98755432 85549732 853549732 53549732 Order C Order D 53549732 85549732 853549732 97855432 98755432 In which order did the other five variants of chomosome 3 most likely arise? O order B O order C O order A 71-20

Q: 4. For a series of breeding experiments, a linkage group composed of genes A, B, C, and D was found…

A: The genes which are present on same chromsome, are inherited together, Such genes are called linked…

Q: To define an SMC (structure maintenance of chromosomes) complex and give two example.

A: Introduction  Chromosomes are thread-like structures found within the nucleus of both animal and…

Q: 2. From previous research findings, you know that the distance between the gene for eye colour and…

A: In flies , there are two types of traits . These are:-  I ) Trait for eye colour :- In this ,purple…

Q: d. sex chromosome do only ma e. Shade the female offspring in the above Punnett square. Leave the…

A: A karyotype is an individual's collection of chromosomes. The term also refers to a laboratory…

Q: Based on these results, what can we claim? Select any/all that apply O There are at least 5 loci in…

A: In the provided Manhattan plot, regions with -log10(P) values exceeding 7 are considered…

Q: Hemophilia and color blindness are both recessive conditions caused by genes on the X chromosome. To…

A: Recombination frequency is defined as the proportion of recombinant offspring produced in a genetic…

Q: Describe two differences among these chromosomes.

A: Chromosome mapping is the arrangement of the chromosomes. Genetic mapping provides a clue about the…

Q: Question 3: If a karyotypically normal egg was to be fertilized by a sperm from question 1, what are…

A: A: 2n=46: This is the normal diploid number for humans, resulting from the combination of 23…

Q: A series of hybrid cell lines was created by somatic human-mouse somatic cell hybridization. Each…

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Q: 6. Why is it necessary for the DNA to replicate prior to cell division? A. so that each daughter…

A: 6. B. so that each daughter cell will have a complete copy of genetic material.  7.  Purple = PP,…

Q: Based on the data above, which of these genes (B, R, or D) is in the middle of the other two, along…

A: The genetic mapping, also called the linkage mapping is a process of identification of relative…

Q: Scenario 2: Down's syndrome can be caused by either a trisomy of chromosome 21 (2n=47 (+21)) or a…

A: Down syndrome is a genetic disorder that can be caused by two main mechanisms:Trisomy 21: This is…

Q: c) What is the probability that the offspring will not have sickle-cell anemia but will be a carrier…

A: c Father genotype = Ss (Heterozygous dominant for not having sickle-cell anemia) Mother genotype =…

Q: If human cells contain the same number of chromosomes, then discuss what account for their…

A: Cells can be thought of as the basic building blocks of all organisms. The human body has billions…

Q: Construct a chromosome map from the following chart showing crossover frequencies for linkage groups…

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Q: When recombination (“crossing over”) doesn’t happen correctly, what type(s) of mutations that can…

A: Crossing over is a process of exchange of chromosomal segments between the non-sister chromatids of…

Q: You are a gene hunter, trying to find the genetic basis for a rare inherited disease. Examination of…

A: It is given that the rare inherited disease is co-inherited with the markers on the chromosome 7 for…

Q: B. Does evervone have a copy of this gene? Explain vour answer.

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A: Note: According to the guidelines, we are supposed to answer only 1 question. Please repost other…

Q: Cells lacking telomerase can grow for several cell divisions without obvious defects. However, after…

A: DNA replication is a process that replicates DNA during every cell division but with each DNA…

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Q: Consider the diagram below and answer the following questions: • The image shows [Select]…

A: Solution)1)Homologous Homologous chromosomes are similar in size, shape, and genetic content. They…

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Q: In each of these diagrams (A-D) homologs are shown as the same size and color. A ANE 1 C B Which of…

A: DNA is our generic career molecule. They are found in nucleus of eukaryotic cell. During propage…

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Q: 13.2 13.1- 12. 11 11- 12 22 23 24 HIDGE b с d f g bo h

A:

Q: If the skin cells of house cats contain 38 homologous pairs of chromosomes, how many chromosomes are…

A: Chromosomes are thread-like structures that carry genes.

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A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: 1. Chris and Emma are phenotypically normal but carriers for SCA (gene A). a. What are their…

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A: Introduction Meiosis is a type of cell division that occurs in sexually reproducing organisms' germ…

Q: Question 14 Short regions of chromosome 1 were sequenced in a population of C. elegans. These…

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Q: The following gene arrangements in a particular chromosome are found in different geographic…

A: The mutation is a sudden and abrupt change in the structure and function of chromosomes.

Q: Chromosomal rearrangement 1 Chromosomal rearrangement 2 centromere A1 B Chromosomal rearrangement 3…

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Q: Nullisomy is a genome mutation where a pair of homologous chromosomes that would normally be present…

A: Chromosomes are long thread-like structures that carry coded genetic information in the form of DNA.…

Q: Referring to Figure 17-19, draw a diagram showing theprocess whereby an inversion formed from…

A: Crossing over refers to the process of transferring genes between related chromosomes. Crossing over…

Q: Suppose the banding pattern variation for chromosome 9 in butterflies arose in the given order. The…

A: The mutation is a change in the sequence of genetic material that occurs as a result of a…

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A: This information in the given pedigree can be solved by: There is a mutation in the progenitor cells…

Q: Part of the karyotype of a diploid individual who is heterozygous for one chromosomal rearrangement…

A: Chromosomal rearrangements are structural changes to chromosomes that affect how the genetic…

Q: Which letter denotes the homologous chromosomes? Group of answer choices C A D b

A: Gene is the sequence of nucleotides that encode a particular protein.

Q: Rainbow trout go through a unique genetic reproductive process. Female eggs are diploid, while male…

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Genome annotation

The technique of linking biological information to genome sequences is termed genome annotation. Gene annotation is the method of identifying gene locations and coding sections. It helps us understand what these genes are doing in the body through establishing structural characteristics and linking them to the actions of various proteins.