Name: inheritance risk with sum and product rules
Uploaded: 2019-03-11T09:21:16.000Z
Duration: 1 min 49 s
Channel: JoVE

K12 Standards

north-carolina-k-12-science-standard-course-of-study

North Carolina K-12 Science Standard Course of Study

9-12

Biology

heredity-inheritance-and-variation-of-traits

Heredity- Inheritance and Variation of Traits

LS.Bio.7.2

Probability Laws

- [강사] 확률에 대한 합과 곱의 법칙은누군가의 특성의 표출에 대한 가능성을 결정하는 데 사용됩니다.예를 들어, 추정 여성의 가계도에서바이오티니다제 결핍과 같은 질병이 나타나며그녀와 배우자가 해당될 지 모르는열성 바이오티니다제 결핍 대립 유전자 보균자의 확률은해당 장애에 대한 자녀의 위험 정도를 결정합니다.이 여성의 가계도에서 한 형제가 질병에 걸린 것을 볼 수 있는데영향이 없는 부모는 이종접합이 분명합니다퍼니트스퀘어는 이 여성이 동형접합으로정상 대립 유전자를 보유하거나 유전으로둘 중 한 부모가 질병 대립 유전자 전했다는 것을 보여줍니다동형접합의 열성 선택권은 무시되는데그녀가 보균자가 될 수 있는 방법이 두 가지이기 때문입니다양쪽 모두 3분의 1 확률입니다그 확률의 합은이 여성의 이질접합 가능성이며, 합의 법칙입니다반대로, 아버지의 확률은 120분의 1입니다임의의 개인에 대한 경우로서 가능성은이형접합입니다추정 부모 둘 다 보균자로서확률이 3분의 2와 120분의 1이며병든 대립 유전자의 전달은4 분의 1의 확률입니다따라서, 자녀가 바이오티니다제 결핍이 생길 가능성은이 확률의 결과입니다대략 0.14 %로서곱의 법칙입니다이는 계산된 이론적 확률이지만일부 커플에게는 자녀만 해당되어바이오티니다제 결핍이 생길 수 있고실증적 확률은 100%로 관측됩니다그러나, 다수의 가계도를 연구한다면이러한 확률은 적용됩니다

그리피스, 앤서니 J.F., 제프리 H. 밀러, 데이비드 T. 스즈키, 리처드 C. 르원틴, 윌리엄 M. 겔바트. 2000. "유전 적 비율 사용." 유전자 분석 소개에서. 7판. 뉴욕 : WH Freeman and Company. [<a href="https://www.ncbi.nlm.nih.gov/books/NBK21812/" target="__blank">소스</a>]

확률 법칙

<h4>개요</h4>
 
 합의 법칙(sum rule)과 곱의 법칙(product rule)을 사용하여 형질을 물려받을 확률을 계산할 수 있습니다. 합의 법칙은 상호 배타적(mutually exclusive) 사건의 확률을 계산하는 데 사용됩니다. 곱의 법칙은 여러 독립된 사건의 확률을 예측합니다. 이러한 확률 법칙은 사건이 발생하기 전 해당 사건이 발생할 가능성인 이론적 확률(theoretical probability)을 결정합니다. 반면, 경험적 확률(empirical probability)은 이미 발생한 사건을 기준으로 계산됩니다.
 
 <h4>합의 법칙과 곱의 법칙을 활용하여 유전 확률을 계산합니다</h4>
 
 퍼넷 사각형(Punnett square)은 한 두 가지 형질의 유전을 시각화하는 데 유용하지만, 더 복잡한 시나리오에 적용하면 번거로워집니다. 세 가지 형질을 나타내는 퍼넷 사각형만 봐도 이미 가능한 교배가 64개나 있습니다. 확률 법칙을 사용하면 형질 유전 확률을 훨씬 효율적으로 계산할 수 있습니다.
 
 비오틴분해효소 결핍증(biotinidase deficiency, 줄여서 BTD) 가족력이 있는 임신부가 자신의 아이가 BTD를 물려받을 위험성을 알아보는 경우를 예로 들어봅시다. BTD는 상염색체 잠성(autosomal recessive) 질환입니다 (주: 우성(dominant) 또는 열성(recessive)이라고 표현할 수 있지만 우성/열성은 현성/잠성으로 개선해야 할 표현입니다). BTD를 치료하지 않은 신생아는 발육 지연, 근육 저하, 피부 발진, 탈모 등의 증상을 보입니다. 심하면 발작, 시력 및 청력 상실과 관련이 있습니다. 임신부와 임신부의 부모님 모두 질환이 없지만, 임신부의 남동생은 질환이 있습니다. 이는 두 부모가 각각 원인 유전자 변이(causal gene variant)을 하나씩 가지고 있을거란 것을 의미합니다 (두 부모가 이형접합자(heterozygote), 즉 보인자(carrier))
 
 임신부의 아이가 BTD을 물려받을 할 확률은 임신부가 자신의 부모처럼 원인 대립유전자(causal allele) 하나를 보유하고 있는 보인자인지 여부에 좌우됩니다. BTD는 상염색체 잠성이며, 임신부는 질환이 없기(unaffected) 때문에 원인 대립유전자 두 개를 가지고 있을리 없습니다. 하지만 아이에게 전달될 수 있는 원인 대립유전자 하나를 가지고 있을 수는 있습니다.
 
 아이가 BTD를 물려받을 위험을 확인하는 첫 번째 단계는 임신부가 보인자일 가능성을 판단하는 것입니다. 여기엔 확률의 합의 법칙을 적용합니다. 합의 법칙은 상호배타적인 사건의 확률은 개별 사건 확률의 합이라고 말합니다. 이 경우 상호 배타적인 사건은 임신부가 물려받았을 수 있는 부모의 대립유전자 조합입니다. 임신부의 부모는 모두 이형접합자(Bb 유전자형(genotype))이기 때문에 임신부는 다음과 같은 가능한 유전자형 네 개 중 하나를 가지고 있습니다: 아버지 B와 어머니 B (BB), 아버지 B와 어머니 b (Bb), 아버지 b와 어머니 B (Bb), 또는 아버지 b와 어머니 B (bb). 일단 임신부가 질환을 가지고 있지 않기 때문에, bb 유전자형을 제외할 수 있습니다. 이렇게 되면 임신부에겐 1/3의 동일한 확률을 가진 3개의 가능한 유전자형이 있으며, 이들 중 2개는 보인자(Bb)입니다. 따라서 합의 법칙에 따르면 임신부가 보인자일 확률은 1/3 + 1/3, 즉 2/3입니다.
 
 아이가 BTD를 물려받을 위험의 또 다른 중요한 요소는 임신부의 반려자가 보인자일 확률입니다. 여기선 곱의 법칙을 적용합니다. 곱의 법칙은 여러 독립된 사건의 확률은 개별 사건 확률의 곱이라고 말합니다. 임신부가 보인자인 경우, 이것은 반려자가 보인자인지 여부에 영향을 주지 않습니다. 따라서 이는 독립적인 사건입니다.
 
 임신부의 반려자도 질환이 없다고 가정했을 때, 아이가 BTD을 물려받으려면 여러 독립적인 사건이 발생해야 합니다. 첫째, 임신부는 꼭 보인자여야 합니다 (앞서 계산했던 2/3 확률). 둘째, 임신부의 반려자도 꼭 보인자여야 합니다. 반려자에게 질환이 없고 BTD의 가족력도 없는 경우 이 사람이 보인자일 확률은 일반 인구에서 보인자가 발견되는 확률(1/120)과 동일한 것으로 간주합니다. 셋째, 아이는 부모 모두에게서 잠성 대립유전자를 물려받아야 합니다 (부모가 모두 보인자인 경우 아이가 잠성 대립유전자를 물려받는 확률은 1/4입니다). 곱의 법칙을 적용하면 아이가 BTD를 물려받을 위험은 다음과 같은 개별 확률의 곱입니다: (2/3) x (1/120) x (1/4) = ~0.0014, 즉 대략 0.14%입니다.
 
 <h4>이론적 확률과 경험적 확률은 사건 전과 사건 후에 각각 따로 계산됩니다</h4>
 
 앞선 예와 같이 출생 전에 계산한 아이가 BTD를 물려받을 확률 0.14%는 이론적 확률입니다. 그러나 아이와 아이의 형제/자매가 BTD를 물려받을 수 있으며 이에 대한 경험적 확률은 100%입니다. 사건이 발생하기 전에 계산되는 이론적 확률과 달리 경험적 확률은 관측에 근거합니다. 하나의 가계도(pedigree)를 분석하는 이론적 확률과 경험적 확률은 크게 다를 수 있습니다. 그러나 더 많은 가계도가 분석될수록 이론적 확률과 경험적 확률은 점점 일치하게 됩니다.

개요

트레이트를 상속할 확률은 합계 및 제품 규칙을 사용하여 계산할 수 있습니다. 합계 규칙은 확률을 계산하는 데 사용됩니다.

Education

교육

JoVE Core

생물학

Genetics

유전학

Classical and Modern Genetics

고전 유전학과 현대 유전학

KEY TERMS AND CONCEPTS

주요 용어 및 개념

inheritance risk with sum and product rules

Inheritance risk can be calculated with the sum rule and the product rule. The sum rule applies to mutually exclusive events, or events that cannot happen at the same time. The product rule applies to independent events, or events that do not affect one another. These rules describe theoretical probability, which is the chance of an event before it happens. Empirical probability is different because it is based on events that have already occurred.

These probability rules are useful in genetics because Punnett squares can become too large for complex crosses. A Punnett square for three traits already has 64 possible crosses. Probability laws make it easier to estimate how a trait may be inherited. They can also be used to follow the chance of an autosomal recessive disease such as biotinidase deficiency, or BTD.

BTD can cause developmental delays, poor muscle tone, skin rashes, and hair loss if it is not treated. Severe cases can also involve seizures and loss of vision and hearing. In the example from the transcript, a pregnant woman is trying to estimate her child’s risk because her brother has BTD. Since her parents do not have the disease but have an affected child, both parents must be carriers, which means they are heterozygotes with one causal gene variant.

The first step is to find the woman’s chance of being a carrier. Because BTD is autosomal recessive and she is unaffected, she cannot have two causal alleles. Her possible genotypes from two carrier parents are BB, Bb, Bb, or bb. The bb genotype can be ruled out, so three outcomes remain, each with a probability of 1/3. Two of those outcomes make her a carrier, so the sum rule gives her a carrier probability of 2/3.

Next, the father’s carrier chance must be considered. If the father is unaffected and has no family history of BTD, his carrier probability is treated as the same as that of the general population, or 1/120. This step uses the product rule because the mother’s carrier status does not change the father’s carrier status. The child must inherit the recessive allele from both parents, which has a probability of 1/4 if both parents are carriers. Multiplying these values gives a BTD risk of about 0.14%.

That 0.14% estimate is a theoretical probability because it is calculated before birth. If a child or siblings actually inherit BTD, that is an empirical result because it is based on observation after the event. When only one pedigree is examined, theoretical and empirical probability may differ a lot. As more pedigrees are studied, the two values tend to become closer.

Inheritance Risk with Sum and Product Rules

genetic lingo

Genotype, Phenotype, and Inheritance

Genotype, phenotype, and inheritance help explain how traits and disease risk are passed from parents to offspring. In diploid organisms, including humans, most other animals, and many plants, somatic cells carry a duplicate set of chromosomes. These chromosome pairs are homologous, with similar length, centromere position, and gene locations. Diploid organisms inherit two versions of each gene, one from each parent. These versions are called alleles, and they sit at the same relative locus,...

punnett squares

Punnett Squares for Predicting Traits

Punnett squares help predict which traits offspring may inherit from two parents. They show possible genotypes, which are pairs of alleles, and can also show the chance of a phenotype, or visible trait, when the inheritance pattern is known. These grids work best for traits controlled by a single gene locus and passed on independently during meiosis. Punnett squares were developed in the early 1900s by Reginald Punnett. His work came after Gregor Mendel’s pea plant experiments revealed the...

monohybrid crosses

Mendel’s Pea Plant Inheritance Ratios

Gregor Mendel used pea plants to study how traits are passed from parents to offspring. His breeding experiments in the 1850s and 1860s showed that inheritance follows clear patterns. He crossed true-breeding plants that differed in one trait and found that dominant traits can hide recessive traits. Mendel focused on seven pea plant traits, and each trait had two forms controlled by a single gene locus. He noticed that true-breeding plants always produced offspring with the same phenotype, or...

dihybrid crosses

Mendel's Law of Independent Assortment

Mendel’s law of independent assortment explains how two traits can be inherited separately. Gregor Mendel tested this idea with pea plants that differed in two characteristics, such as pea color and pea shape. He used true-breeding parents that were homozygous for both traits but showed different phenotypes. In one example, Mendel crossed round, yellow peas with wrinkled, green peas. The parental generation had RRYY and rryy genotypes. Their first-generation offspring were all dihybrids,...

law of segregation

Mendel’s Pea Cross Ratios

Mendel’s pea plant crosses show how traits can disappear in one generation and return in the next. When he crossed plants, one parental trait sometimes seemed to vanish in the F1 generation and reappear in the F2 generation. Mendel used this pattern to explain why some traits are dominant and others are recessive. He proposed that traits are controlled by alleles, which are different versions of a gene. An organism inherits two copies of each gene, one from each parent. In his model, a...

law of independent assortment

Mendel’s Dihybrid Cross and Trait Ratios

Mendel’s dihybrid cross shows how two traits are inherited at the same time. A dihybrid cross is a cross in which both parents are homozygous for two distinct traits, and the F1 generation is heterozygous for both traits. Mendel used pea plants with round yellow peas and wrinkled green peas as an example. One parent had genotype YYRR, and the other had genotype yyrr. In the F1 generation, every plant showed the dominant traits, so the plants were YyRr and had yellow, round peas. The F2...

probability laws

Inheritance risk can be calculated with the sum rule and the product rule. The sum rule applies to mutually exclusive events, or events that cannot happen at the same time. The product rule applies to independent events, or events that do not affect one another. These rules describe theoretical probability, which is the chance of an event before it happens. Empirical probability is different because it is based on events that have already occurred. These probability rules are useful in...

test cross

Using Test Crosses to Identify Genotypes

Test crosses are used to identify the genotype of an organism with a dominant trait. A genotype is the pair of alleles inherited for a gene, and alleles are different forms of the same gene. In diploid organisms, including humans, each gene usually has two alleles, one from each parent. An allele is recessive when its effect is hidden by another allele at the same gene location. Pea plants provide a clear example with flower color. White flowers are recessive, because one copy of the purple...

polygenic traits

Polygenic Traits in Human Height

Polygenic traits are traits controlled by more than one gene. Human height is a clear example of this kind of inheritance. Because many genes work together, the final trait can vary a lot from person to person. Researchers have found hundreds of loci, or gene locations, that influence height. There are likely many more that have not yet been identified. Many of these genes affect cartilage in the growth plates of the long bones in the arms and legs, either directly or indirectly. Height is...

pedigree analysis

Reading Family Traits in Pedigrees

Pedigrees are family trees used to track how a trait passes through generations. They help scientists and students see whether a trait is dominant or recessive, whether it is autosomal or sex-linked, what genotypes family members may have, and what phenotypes may appear in future generations. For families with a history of inherited disease, this information can be important for family planning. In plants and animals, inheritance is often studied with crosses. Monohybrid crosses can show...

multiple allele traits

Blood Type and Allele Interactions

Multiple alleles can shape traits through blood type, sickle cell anemia, incomplete dominance, and codominance. Multiple allelism means a gene has three or more allelic forms. Diploid organisms, including humans, usually carry only two alleles for each gene, but many human genes exist in multiple forms in the population. Human blood type is a clear example of multiple allelism. The blood type gene has three alleles: I A , I B , and i. These alleles help determine which blood type a person has...

epistasis

Gene Masking in Rabbit Fur Color

Epistasis describes how one gene can mask or change the effect of another gene. In high school genetics, this helps explain why many traits do not follow a simple single-gene pattern. Instead, alleles at different locations can work together to shape the final phenotype. Mendel studied seven unrelated pea traits, but most traits involve multiple gene interactions. Epistasis often happens when one gene interferes with the expression of another gene. It can also occur when genes are part of the...

nature and nurture

Genes and Environment Shape Height

Genes and environment both shape human height and other traits. Genes are the inherited instructions we get from our parents. Environment includes factors such as diet, stress, and social conditions. Many phenotypes, or observable traits, reflect both influences. Some also show up later in life, including cancer and other diseases. Height is a clear example of this interaction. Scientists estimate that 70-90% of height variation comes from genetic differences among people. The remaining 10-30%...

pleiotropy

SOX10 and Multiple Traits in Pleiotropy

Pleiotropy is when one gene affects more than one trait. The SOX10 gene is a clear example because it can influence pigmentation, hearing, and intestinal movement. These traits may seem unrelated, but they can all be linked to the same gene change. In humans, a deleted region in SOX10 can cause Waardenburg Syndrome Type 4, or WS4. WS4 is an autosomal recessive disorder, which means a person usually inherits two altered copies of the gene. Common signs include a white forelock,...

sex-linked disorders

X- and Y-Linked Disorder Patterns

X- and Y-linked disorders come from mutations in genes on the sex chromosomes. These genes, like those on autosomes, are needed for normal body function. When a mutation causes a biological problem, the condition is called sex-linked. Y-linked disorders come from changes in the Y chromosome. They affect only males, because only males carry a Y chromosome. Mutations in this small chromosome can affect male sexual function and secondary sex characteristics. One example is Y-chromosome...

x-linked traits

X-Linked Inheritance in Families

X-linked inheritance explains how traits on the X chromosome are passed through families. In most mammalian species, females have two X sex chromosomes, while males have one X and one Y. A mutation on one X chromosome may be masked in females by a normal allele on the other X. In males, that same mutation is more likely to show because there is no second normal X to balance it. Traits caused by changes on the X chromosome are called X-linked traits. Color blindness is a well-studied example.

x-inactivation

Barr Bodies and X-Chromosome Balance

Barr bodies and X-chromosome balance help explain how female mammalian cells control gene activity from the X chromosome. The human X chromosome carries far more genes than the Y chromosome. Because males usually have one X chromosome and females have two, females would make twice as many of some proteins without a control system. To prevent that imbalance, female mammalian cells inactivate nearly all the genes on one X chromosome during early embryonic development. The inactive X condenses...

non-nuclear inheritance

Maternal DNA in Mitochondria and Chloroplasts

Maternal DNA in mitochondria and chloroplasts explains how some genes are inherited outside the nucleus. Most DNA is in the nucleus, but mitochondria and chloroplasts in the cell cytoplasm also carry their own DNA and can copy it independently of nuclear DNA. Mitochondria are found in both plant and animal cells. They are called the powerhouses of eukaryotic cells because they break down glucose to make energy for cellular activity. Mitochondrial DNA has about 37 genes, and many help with...

chromosomal theory of inheritance

How Genes Map to Chromosomes

Genes map to chromosomes, and this idea explains how Mendel’s inheritance patterns work. Gregor Mendel published his pea plant breeding results in 1866. He showed that physical traits follow predictable patterns. At the time, scientists did not yet know that genes existed. Mendel used the word "factors" for the hereditary units he studied. The details behind Mendel’s laws of segregation and independent assortment were still unknown for many years. In the late 1800s, better microscopes and...

key terms and concepts

Learn how the sum rule and product rule help estimate inherited trait risk, including carrier probability and autosomal recessive disease examples like BTD.

Inheritance Risk with Sum and Product Rules | JoVE K12

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Minnesota Academic Standards in Science

Life Science

2.1.1 9L.2.1.1.1

new-jersey-student-learning-standards-for-science

New Jersey Student Learning Standards for Science

High School

Heredity: Inheritance and Variation of Traits

HS-LS3-3

Alabama Course of Study Science

9-12.B.3.11

Next Generation Science Standards

HS-LS3-1

new-york-state-science-learning-standards

New York State Science Learning Standards

Inheritance and Variation of Traits

HS-LS3-1.

HS-LS3-3.

myJoVE Corporation

What is Meiosis?

Meiosis is the process by which diploid cells divide to produce haploid daughter cells. In humans, each diploid cell contains 46 chromosomes, half from ...

Meiosis I

Meiosis II

Meiosis vs. Mitosis

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to ...

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This ...

Spermatogenesis

Spermatogenesis is the process by which haploid sperm cells are produced in the male testes. It starts with stem cells located close to the outer rim of ...

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from ...

Fertilization

During fertilization, an egg and sperm cell fuse to create a new diploid structure. In humans, the process occurs once the egg has been released from the ...

Cleavage and Blastulation

After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage ...

Gastrulation

Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of ...

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three ...

Cell Migration

Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms ...

Determination

During embryogenesis, cells become progressively committed to different fates through a two-step process: specification followed by determination. ...

Use models to explain how DNA is passed from parents to offspring through the processes of meiosis and fertilization in sexual reproduction.

LS.Bio.6.1

Mutations

Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations ...

genome-size-and-the-evolution-of-new-genes

Genome Size and the Evolution of New Genes

types-of-genetic-transfer-between-organisms

Types of Genetic Transfer Between Organisms

Base-pairing and DNA Repair

The DNA Replication Fork

Lagging Strand Synthesis

The Replisome

Proofreading

Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template ...

Replication in Prokaryotes

DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the ...

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before ...

Overview of DNA Repair

Base Excision Repair

Nucleotide Excision Repair

DNA Distortion and Damage
Cells are regularly exposed to mutagens&#8212;factors in the environment that can damage DNA and generate mutations. UV ...

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the ...

Fixing Double-strand Breaks

Homologous Recombination

Gene Conversion

Restarting Stalled Replication Forks

Construct an explanation to summarize how inheritable genetic variations may result from: new genetic combinations in meiosis, mutations during replication, or mutations caused by environmental factors.

LS.Bio.6.2

An Overview of Genetic Analysis

An organism&#8217;s physical traits, or phenotype, are a product of its genotype, which is the combination of alleles (gene variants) inherited from its ...

Genetic Crosses

To dissect genetic processes or create organisms with novel suites of traits, scientists can perform genetic crosses, or the purposeful mating of two ...

Punnett Squares

Monohybrid Crosses

Dihybrid Crosses

Trihybrid Crosses

Trihybrid Crosses
Some of Mendel&#8217;s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A ...

Law of Independent Assortment

Chi-square Analysis

The chi-square test is a statistical hypothesis test. It is used to check whether there is a significant difference between an expected value and an ...

Pedigree Analysis

Multiple Allele Traits

Incomplete Dominance

Gregor Mendel&#39;s work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid ...

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cu&#233;not discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is ...

Polygenic Traits

background-and-environment-affect-phenotype

Background and Environment Affect Phenotype

Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as ...

Use mathematics and computational thinking to predict the variation and distribution of expressed traits based on: Mendelian inheritance, co-dominance, incomplete dominance, multiple alleles, and sex-linked inheritance.

LS.Bio.7.1

Overview

A pedigree is a diagram displaying a family&#x2019;s history of a trait. Analyzing pedigrees can reveal (1) whether a trait is dominant or ...

Overview

The probability of inheriting a trait can be calculated using the sum and product rules. The sum rule is used to calculate the probability of ...

The Concept of Multiple Allelism

Multiple allelism describes genes that exist in three or more allelic forms. Although diploid organisms, like humans, ...

Analyze and interpret data to explain how polygenic traits result in a wide range of phenotypes.

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause ...

Nature and Nurture

Many human characteristics, like height, are shaped by both nature&mdash;in other words, by our genes&mdash;and by nurture, or our environment. For ...

Construct an explanation to summarize how traits result from interactions of genetic factors (multiple genes and/or alleles) and environmental factors.

LS.Bio.7.3

PCR: The Polymerase Chain Reaction

The polymerase chain reaction, or PCR, is a technique used to amplify DNA through thermocycling &#8211; cyles of temperature changes at fixed time ...

DNA Gel Electrophoresis

DNA gel electrophoresis is a technique used for the detection and separation of DNA molecules. An electric field is applied to a gel matrix comprised of ...

Analyze and interpret data to compare DNA samples.

LS.Bio.8.1

Understand genetic mechanisms for variation.

Inheritance Risk with Sum and Product Rules

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