Sunday, May 8, 2011
Animal Indexing
These last few weeks I had to walk around my neighborhood counting the animals I saw. I had to do this 4 times each 30 mins long. I counted 14 dogs and 1 cat in my neighborhood. They were all owned. This is after the company spayed and neutered all the dogs and cats. They were having us count the number of stray dogs we saw on our walk so they know if their experiment of spaying and neutering the animals would bring down the number of stray dogs. So far it seems like it is working.
Thursday, April 21, 2011
DNA Detective Work
DNA DETECTIVE WORK
Unless you have a twin, no one in the world has a DNA sequence identical to yours. Although 99 percent of the DNA is the same in all humans, certain segments vary widely. Differences in these segments are detected through DNA fingerprinting. A small amount of tissue, such as blood, hair, or semen, is all that is needed to create a DNA fingerprint. The sample is cut up using enzymes and the segments are separated by size through gel electrophoresis. DNA is made visible either with radioactive probes or by staining. This reveals a pattern of bars: the DNA fingerprint. If the two DNA fingerprints match, they probably came from the same person. If they don't match, they certainly came from different individuals. In recent years, a number of people convicted of crimes have been exonerated based on DNA evidence.
Activity
In this exercise, you will learn the basics of DNA fingerprinting and consider the use of DNA in criminal investigations.
Part 1.
Use your browser to go to NOVA’s web site about “Killers Trail,” the story behind the man who inspired the Fugitive TV series and later the movie version starring Harrison Ford:
Click on the “Chronology of a Murder” section and read about the events that led up to the murder trial of Dr. Sam Sheppard.
1.In your opinion, what role (if any) did newspaper stories and editorials have in the outcome of the original trial of Dr. Sam Sheppard?
The newspaper stories and editorials blamed Dr. sam Sheppard even though he was innocent.
Go back to the Killers Trail homepage and select ”Create a DNA Fingerprint.”
Read about the crime and the suspects then go on to part 2. Answer the following questions about the technique as you go through the simulation:
2.What is the function of the restriction enzymes in DNA fingerprinting?
The restrictive enzymes act like scissors to cut the DNA
3.What is the function of the agarose gel electrophoresis step?
The agarose gel acts like a molecule strainer.
4.Why is a nylon membrane used to blot the DNA?
Because the agarose gel is difficult to work with.
5.What does a dark spot on the X-ray film indicate?
The dark spot on the xray film represented the DNA sequence.
Part 2.
Use your browser to go to Frontline's "What Jennifer Saw" at
The material on this site is about a man convicted of rape but later exonerated by DNA evidence. To read a summary of the case, choose the link to Ronald Cotton's wrongful conviction, then choose "Summary of Cotton's Case."
In the interviews section, read the interviews with DNA expert Peter Neufeld and lawyer Barry Scheck.
Answer the following questions:
6.What evidence was initially used to convict Cotton?
The evidence used to convict cotton was a photo id was made by one of the victims. A police lineup id was made by one of the victims. A flashlight in cottons house resembled the one used by the assailant. And last rubber from cottons shoes were consistent with rubber found at one of the crime scenes.
7.What did the DNA evidence show?
The DNA evidence showed it was not cotton that committed the crime but the guy in prison that had already admitted to cottons crimes
8.How could DNA fingerprinting be used to prevent a false conviction if a case like this was being tried today?
DNA fingerprinting could save a guy from being committed for a crime they didn't do by testing the DNA evidence and the DNA of the assailent.
9.What percentage of convicts are unjustly convicted of sexual assault cases, according to Neufeld and Scheck?
25% of convicts are unjustly convicted of sexual assault cases.
10.The O.J. Simpson trial was one of the most visible trials that attempted to use DNA evidence. In the end, the DNA evidence was not satisfying to the jury, who acquitted Simpson. What do Neufeld and Scheck believe about the impact of the O.J. Simpson trial on the use of DNA evidence?
The oj simpson trial made people in prison who are innocent try to use dna to get out of their crimes.
Wednesday, March 30, 2011
DNA Sequencing Graph
As you can see in the graph Abby and Bob are both 97% from normal and Carol is 58%. Abby has point mutation wrong with his DNA. this means that one point is wrong with his.Bob has truncation mutation. This means one point is wrong with his but that point caused the DNA to add a stop. so everything after the stop doesn't matter. so really Bob is 79%. the last is carol she is at 58% because she has a frame shift mutation. one letter was missing so all the rest of the letters shifted over and made her entire DNA wrong. All three people have a chance of having a disease but we don't know them so we can't tell. We are pretty sure carol has a disease though.
Tuesday, March 15, 2011
DNA extraction lab
A few days ago we did a DNA extraction lab. It was really cool first we mixed wheat germ water and soap together. None of us knew what we were doing. then when we added the alcohol the DNA started to rise into the alcohol. It looked like a booger. My group didn't think about getting a picture of it for our blogs, so we didn't, too bad.
Saturday, March 5, 2011
Eugenics
Eugenics is a very interesting subject. In this post I will go through what eugenics are, what is the social and scientific origins of eugenics, How they researched it, and finally how it impacted America.
Eugenics is the study of or belief in the possibility of improving the qualities of the human species or a human population, especially by such means as discouraging reproduction by persons having genetic defects or presumed to have inheritable undesirable traits (negative eugenics) and encouraging reproduction by persons presumed to have inheritable desirable traits. This was started in the united states of America. Only instead of just trying to discourage people with genetic defects from having kids. They sterilized them so they couldn't have kids. They also wanted to improve humanity by encouraging the blessed and healthiest people to have more children.
The social origins of eugenics was it explained the causes of pauperism, feeble-mindedness, alcoholism, rebelliousness, nomadism, criminality, and prostitution as the inheritance of defective germ plasm. Eugenicists said society paid a high price by allowing the birth of defective individuals who would have to be cared for by the state and Sterilization of one defective adult could save future generations thousands of dollars. Eugenics was seen as a way to solve all of these problems because it placed the cause in the defective germ plasm of individuals and ethnic groups, and not society itself. Eugenics used the cover of science.
Francis Galton made up the word eugenics. Positive eugenics is encouraging the blessed and healthiest people to have more children. negative eugenics is when stopping the less fit people from having kids. Germany and the united states did the negative approach. Indiana law enacted in 1907 compulsory sterilization of "degenerates", the First Eugenic Sterilization Law in the United States. people caught masturbating were known as degenerates and then sterilized them to stop the degeneracy gene.
Eugenics research started with Mendel’s laws of inheritance of human traits. Also known as independent assortment which states that alleles of different genes assort independently of one another during gamete formation. By examining pedigrees eugenicist attempted to make a pattern of one of these three basic modes of inheritance either recessive, dominant, or sex-linked. They had to find big families and score each member of the family of the absence or presence of a trait. This would work but where they messed up on back then was they attempted to measure complex traits like intelligence or musical ability or complex mental illnesses like schizophrenia or manic depression.
Eugenics did many things for America. The first and biggest thing it did was bring the crime rate down. They made us more educated. Also they tried to save the future generations money. The last thing they did for a America was made us a pure race.
This was an interesting subject. I'm kind of interested to learn more about it and wonder if we or other countries still do this only smarter.
Sunday, February 27, 2011
INVESTIGATING INDEPENDENT ASSORTMENT
INVESTIGATING INDEPENDENT ASSORTMENT
Mendel observed the effects of independent assortment when he carried out his dihybrid crosses. When he crossed two plants that bred true for different versions of two traits, the first-generation offspring all displayed the same phenotype (the dominant phenotype for both traits). However, when these plants were crossed, the second-generation offspring included four different phenotypes.
Mendel carefully recorded the numbers of phenotypes among the offspring of many dihybrid crosses. He found that certain combinations of phenotypes among the second-generation offspring occur in a 9:3:3:1 ratio, on the average. We now know that this pattern occurs because genes on pairs of homologous chromosomes are sorted out for distribution into one gamete or another independently of gene pairs of other chromosomes.
Activity
In this activity, you will first access the meiosis tutorial provided by the University of California, Santa Barbara. The tutorial demonstrates the random assortment of chromosomes into gametes. Next you will complete a tutorial quiz about independent assortment. This is part of The Biology Project from the University of Arizona.
Part 1.
Use your browser to go to the meiosis tutorial at
Use the tutorial to learn how to determine which allele combinations are possible in two or even three trait crosses.
Part 2.
Use your browser to go to the independent assortment tutorial at
Go through questions 1-9 of the tutorial. If you answer any question incorrectly, review the tutorial material and try again.
When you have completed this much of the tutorial, answer the questions below:
1. What type of gametes will be produced by a plant of genotype AaBb?
The gametes produced be a plant with genotype AaBb would be AB or Ab or aB or ab
2. What type of gametes will be produced by a plant of genotype aabb?
The gametes produced be a plant with genotype aabb would be ab
3. List all the genotypes you would find among the offspring of an AaBb x aabb test cross.
The genotypes would be AaBb, aaBb, Aabb aabb
4. What is the expected phenotypic ratio of the offspring of an AaBb x aabb test cross?
The expected phenotypic ratio of the offspring of an AaBb x aabb would be 1:1:1:1
5. List all possible gametes from a trihybrid individual whose genotype is RrSsTt.
The possible gametes for a trihybrid individual with a genotype RrSsTt would be RST or rst or RsT or RSt or rST or rsT or rSt
In sickness and in health
Autosomal dominant disorders cannot skip generations because they are dominant genes so they will show up if the person has it. They can't just be a carrier. So Greg and his mother can't be carriers of myotonic dystrophy. Greg's aunt or uncle can't be homozygous because their mother is the only one with the disorder. Also Greg's mom and one of his uncles doesn't have it. Greg's cousin has a 50% chance of inheriting the gene. Greg and Olga's children have a 0% chance of inheriting the gene because it is a dominant gene and neither Greg nor Olga have the gene.
There are five hallmarks of autosomal recessive inheritance: The first is Males and females are equally likely to be affected. The second is On average, the recurrence risk to the unborn sibling of an affected individual is 1/4. The third hallmark is The trait is characteristically found in siblings, not parents of affected or the offspring of affected. The forth hallmark is Parents of affected children may be related. The rarer the trait in the general population, the more likely a consanguineous mating is involved. The last hallmark is the trait may appear as an isolated (sporadic) event in small sibships. Consanguineous means the amount of shared (identical) DNA or the genetic material. This concept is important when discussing recessive genetic disorders because it means they have some of the same genetic material so they have more of a chance of inheriting the same genes. The factor VIII deficiency is sex linked and not An autosomal recessive trait because it only effects males.
The characteristics of x linked recessive inheritance are the disease is never passed from father to son. Males are much more likely to be affected than females. If affected males cannot reproduce, only males will be affected. All affected males in a family are related through their mothers. Trait or disease is typically passed from an affected grandfather, through his carrier daughters, to half of his grandsons. A son never inherits his fathers infected X-Chromosome because A son inherets the fathers Y-Chromosome from his father and one of his mothers X-Chromosomes. For a women to display a sex-linked recessive trait she would need to inherit two infected X-Chromosomes. One from her father and one from her mother. It is 1/2 chance that olga is a carrier of Factor VIII deficency. She has a 1/2 chance of passing it off on to her offspring. Male and female childern will be affected differently because a female child will just be a carrier becasue she will inheret a normal gene from her father where a amle child will show the trait because they don't have a spare X-Chromosome. Their is a 0% chance Greg is a carrier of factor VIII defeicy because he would have to show it not just carrie it because males don't have a spare X-chromosome.
The link to the population genetics wont work so i couldn't find the second equation to help figure out the the rest of the questions. If i get the equation i will update this blog and finish it.
Some of the legal risks and benefits of genetic testing are there is a chance you wouldn't be able to get health insurance because of a preexisting conditions or your insurance will be higher because they know you have a disorder but it hasn't showed yet. The benefits are you Know you have it so you can start doing things to try to prevent it. An unintended consequence of genetic testing could be that people would be less liable to seek medical care out of fear that they could later be denied life or health insurance. Privance laws and laws preventing insurance companys from deneying a person because they have a preexising conditing.
There are five hallmarks of autosomal recessive inheritance: The first is Males and females are equally likely to be affected. The second is On average, the recurrence risk to the unborn sibling of an affected individual is 1/4. The third hallmark is The trait is characteristically found in siblings, not parents of affected or the offspring of affected. The forth hallmark is Parents of affected children may be related. The rarer the trait in the general population, the more likely a consanguineous mating is involved. The last hallmark is the trait may appear as an isolated (sporadic) event in small sibships. Consanguineous means the amount of shared (identical) DNA or the genetic material. This concept is important when discussing recessive genetic disorders because it means they have some of the same genetic material so they have more of a chance of inheriting the same genes. The factor VIII deficiency is sex linked and not An autosomal recessive trait because it only effects males.
The characteristics of x linked recessive inheritance are the disease is never passed from father to son. Males are much more likely to be affected than females. If affected males cannot reproduce, only males will be affected. All affected males in a family are related through their mothers. Trait or disease is typically passed from an affected grandfather, through his carrier daughters, to half of his grandsons. A son never inherits his fathers infected X-Chromosome because A son inherets the fathers Y-Chromosome from his father and one of his mothers X-Chromosomes. For a women to display a sex-linked recessive trait she would need to inherit two infected X-Chromosomes. One from her father and one from her mother. It is 1/2 chance that olga is a carrier of Factor VIII deficency. She has a 1/2 chance of passing it off on to her offspring. Male and female childern will be affected differently because a female child will just be a carrier becasue she will inheret a normal gene from her father where a amle child will show the trait because they don't have a spare X-Chromosome. Their is a 0% chance Greg is a carrier of factor VIII defeicy because he would have to show it not just carrie it because males don't have a spare X-chromosome.
The link to the population genetics wont work so i couldn't find the second equation to help figure out the the rest of the questions. If i get the equation i will update this blog and finish it.
Some of the legal risks and benefits of genetic testing are there is a chance you wouldn't be able to get health insurance because of a preexisting conditions or your insurance will be higher because they know you have a disorder but it hasn't showed yet. The benefits are you Know you have it so you can start doing things to try to prevent it. An unintended consequence of genetic testing could be that people would be less liable to seek medical care out of fear that they could later be denied life or health insurance. Privance laws and laws preventing insurance companys from deneying a person because they have a preexising conditing.
Subscribe to:
Posts (Atom)

