This image shows electrophoresis results for 3 microsatellite markers (D8S1179, D12S91 and D19S433) that are part of a DNA fingerprint analysis of a crime scene DNA sample. Assuming random mating, use the frequency information for each allele detected here to calculate the probability that a person in the general population will have the genotype shown here for these three markers. O 0.00076 or 0.0756% O 0.00019 or 0.019% O 0.00055 or 0.055% O 0.30 or 30% X
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- Search the menus (Alt+/) 75% Normal text Calibri в IUA 11 + ... 1.| 2 | 3 | • 4.| 5 6 8 12. Although Laurlanthalasa, Princess of the Qualinesti elves, is known for riding into battle on a silver dragon, this is not her main form of transportation. She generally travels by way of griffon. Although the allele for a "crown" of feathers around the head is dominant, it is rarely found in the wild. This may be due to the fact that it makes the griffons stand out, thus making them less effective hunters and more visible to their natural enemies, evil chromatic dragons. This scarcity also makes them prized by elven royalty. Lauralanthalasa was given a breeding pair of bald griffons by an admirer who claims that they are both hybrids for the crowned gene. Create a Punnett Square to determine if Lauralanthalasa will have any chance using these two griffins to produce crowned offspring. Alleles (letters) and Phenotypes All Genotype and Phenotype Parent Punnett Square Possibilities Genotypes…Cierra Ballierajh - Pedigree - Go × + resentation/d/1vcm90PtSWx93LtacvlAUJk84UPuJ9DpU8nS94-XrBPQ/edit#slide-id.g97df83752a_0_315 Fit Co add speaker notes 4× ☆ C Quick... 20 + BIUA - PEDIGREES: Problem 7 (continued) This pedigree shows the inheritance of a type of X-linked color blindness. It is a recessive trait. Carriers have NOT been half-shaded in this pedigree. I 어디어디 2 3 4 II 1 2 3 QUESTIONS ... 3. Use the letter "b" to represent the color blindness allele. What is the genotype of individual IV-I? bb 4. What evidence is there that this type of color blindness is recessive? III IV C 3 Emmatheteachie 2020 65°F Prt Scn Home EndCodominance ABO blood typing is an example of codominance, where A and B are both dominant to O. A woman who is AB type has a child with a man who is O type. Use I allele formatting to designate each genotypes: IA IA, IA i, IB IB, IB i, IA IB, ii A) List the genotype of each parent. B) Complete a Punnett square. List all the genotypes for the predicted offspring of this mating (using the format of genotypes listed above) C) What is the probability that any of their offspring will be O type? D) What is the probability that any of their offspring will be AB type?
- I need some help with this fill-in-the-blank problem. The answer choices are bolded and bracketed. Please see the attached photo to complete. 1. In the D2S441 locus, Sophie's allele [10, 12] is maternal and her allele 10 is paternal from [Sam or Bill only, Sam or Harry only, Bill or Harry only, Sam Bill or Harry (either 3)]. 2. Sophie's allele 13 for D19S433 is [maternal, paternal] and her allele 14 could have come from [Sam and Bill only, Sam and Harry only, Bill and Harry only, Sam Bill or Harry (either 3)]. 3. In the FGA locus, Sophie's allele [21, 22] is maternal and her other allele could have come only from [Sam, Bill, Harry]. 4. Based on all STRs in the 3 panels we studied, it is clear that [Sam, Bill, Harry] is Sophie's father. He has one allele of Sophie's alleles for all STR loci 5. Would these results stand in court as proof paternity: [Yes or No] 6. This type of DNA profiling can also be used to determine maternity. Is there any doubt that Donna is Sophie's biological…FAlpQLSfiOhfAvlhxzCSiUll_6rt-nU5b0WI73UmWOxkOw8OCwk01ng/formResponse B 1 2 Bb x Bb b 4 The fur in both parents in this cross is * 1 B B Bb x Bb b 3 4 brown black O homozygous dominant homozygous recessive 3. 近5 & :56M ******* 24 DIHYBRID CROSSES DRV 0 Stv T alı A @ zladenA 9160p2-id2 bns obidalbaneoviene da II\ MOD YR 21 $59A ... Create a dihybrid cross and determine the expected phenotypic percentages of the offspring of two corn plants both of which are heterozygous for colour and texture (RrTt X RrTt). Don't forget to include clear let statements, and follow the all six steps taught on solving genetics problems. insig moni nellog: bna. zoom
- CH 1-4 X с Maya S x Credib x app.wizer.me/learn/00E0AB wizer.me a Maya X A To-do 25% The table gives the genoty Assign x M Dashb x 50% Figurat X C In cows, brown (B) is codominant with white (W). The heterozygous phenotype is brown and white speckles. A farmer decided to cross a brown cow and a white cow in hopes of making all brown and white speckles. What percentage of the offspring will be brown with white speckles? Figurat X 75% Dashboard Incomp X d Interac X Enter class code Go 100%Edio | Calendar X Edio | Student Da x days/1089977/lessons/1533969/variants/2439102/take/10/ A Q TEXT ANSWER The inheritance patterns for some traits in guinea pigs are listed in the table below. 1. Identify the phenotype of a guinea pig with the genotype HhBBrr. 2. Using the allele symbols in the table, identify the genotype of a guinea pig that is recessive for hair length, heterozygous for hair color, and homozygous dominant for hair texture. Trait Dominant Allele Recessive Allele hair short (H) long (h) length hair color black (B) white (b) rough (R) smooth (r) hair texture BIUG X₁ X¹ EEAA H Normal : √x Enter your answer here ŏooooo Questions Answered 中山川 Ω Ο Τ Edio | Calendar X RepostExchange X Practice All Changes Saved ContinueA single allele gives rise to the Hbs form of hemoglobin. Individuals who are homozygous for the allele (HbS/HbS) develop sickle-cell anemia (Section 9.6). Heterozygous individuals (HbA/HbS) have few symptoms. A couple who are both heterozygous for the HbS allele plan to have children. For each of the pregnancies, state the probability that they will have a child who is: a. homozygous for the HbS allele b. homozygous for the normal allele (HbA) c. heterozygous: HbA/HbS
- How many different genotypes will be expected from a selfing of an individual with the gènotype A/a; B/b; D/D; e/e; F/f? O64 O 16 27/d/1n5NtidRwTwUzcDkDPi5Z9P_SHPZ91A-XH-pfftLbhNc/edit (1) O pols Add-ons Help Last edit was seconds ago BIUA ミ: 12 + ext Calibri I|1 6 I 2 Section 5: Trihybrid cross and Laws of probability For a trihybrid cross, in which inheritance of alleles for three genes is tracked, drawing a Punnett square that combines all three genes may not be practical. Instead the laws of probability may be used. The product law of probabilities says that when alleles for separate genes segregate independently, we can figure out the probability of a particular combined genotype by multiplying the probability of the alleles for each gene. 13. We cross a homozygous tall pea plant with yellow, round seeds to a homozygous dwarf pea plant with green, wrinkled seeds. All the F1 offspring are all tall plants with yellow, round seeds. a. What are the expected F2 ratios (use fractions) of tall and dwarf plants? b. What are the expected F2 ratios (use fractions) of yellow and green seeds? C. What are the expected F2…CYSTIC FIBROSIS LAB EXERCISE INSTRUCTIONS: a hereditary disease that affects the lungs and digestive system DNA SEQUENCE IN FUNCTIONAL (UNAFFECTED) CFTR ALLELE BACKGROUND INFORMATION: DNA Gene Base ancestral Sequence: .... TAG/TAG/AAA/CCA/CAA.... Associated gene: CFTR at locus 7q31.2 • 188,702 bases long • Codes for the CFTR protein, which has 1,480 amino acids • CFTR protein controls chloride ion (salt) & water balance in epithelial cells - surface barrier cells, covering both external and internal surfaces (examples: in the lungs and digestive tract) 1. Transcribe into five MRNA Codons: 2. Translate into five TRNA Anticodons: 3. Identify the five associated Amino Acids: Mutation and Associated Genetic Condition 1,700+ identified mutations that cause protein disfunction • AFS08 CFTR mutation (A = deletion) o accounts for c. 70% of cystic fibrosis cases o estimated origin 52,000 years ago o produces a misfolded, non-functional protein that is discarded o Inheritance: Autosomal…