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EOC Practice Quiz (5) - Duplin County Schools
EOC Practice Quiz (5) - Duplin County Schools

Evolution: Mutation
Evolution: Mutation

... Mutation is one of the four forces of evolutionary change: mutation, genetic drift, gene flow, and natural selection. Mutation is mainly involved with DNA changes. Which of the following is not a type of DNA mutation? A. Substitution B. Insertion C. Deletion ...
Leukaemia Section t(1;12)(p36;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(1;12)(p36;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... anomaly ...
Practice Exam- KEY - mvhs
Practice Exam- KEY - mvhs

... b) No. A frameshift will occur. This will change all the amino acids after K. There will no longer be the signal sequence, so the Stfn4 protein will not be secreted. c) Yes. GUG stands for valine which also, this is a silent mutation. There will be no effects. d) No. GAG stands for Glutamic Acid (a ...


... • State what is meant by a gene • State that mRNA carries the genetic code from DNA in the nucleus to a ribosome for protein synthesis • Describe how a protein is synthesised at a ribosome • Explain how the sequence of DNA bases determines protein structure and function ...
Warm-Up 2/26 and 2/27
Warm-Up 2/26 and 2/27

... malaria (Plasmodium can’t infect sickle shaped cells) ...
Student Handout - University of California, Irvine
Student Handout - University of California, Irvine

...  As the pieces of DNA move through the gel matrix, they will meet resistance. ____________ pieces of DNA will have more difficulty moving through the gel than ___________ fragments. Thus, larger fragments will move _____________ than smaller fragments. This allows separation of all different ______ ...
GBE 305 MOLECULAR BIOLOGY II
GBE 305 MOLECULAR BIOLOGY II

... Total Hours : 75 ...
Bio 139 Exam Review Outline: Exam #3
Bio 139 Exam Review Outline: Exam #3

... RNA polymerase: synthesizes RNA from a DNA template. What is a codon? How many nucleotides does it take to encode one amino acid?(3) What is the “genetic code” and how is it “degenerate”? Know that some codons mean “stop” (don’t need to memorize which ones). tRNAs have two functional ends: one binds ...
CS691K Bioinformatics Kulp Lecture Notes #0 Molecular
CS691K Bioinformatics Kulp Lecture Notes #0 Molecular

Genetics & Prenatal Development
Genetics & Prenatal Development

... Sex Linked Traits • The sex chromosomes, the 23rd pair of chromosomes, determine biological sex • In females, the 23rd pair of chromosomes is made up of two large X chromosomes. XX • In males, a large X chromosome and a smaller Y chromosome make up the 23rd pair. XY • For males, the smaller Y chrom ...
Bacterial Transformation
Bacterial Transformation

... BRIDGES 2014 ...
Epigenetics - Louisiana State University
Epigenetics - Louisiana State University

... Louisiana State University ...
DNA replication - Understanding Evolution
DNA replication - Understanding Evolution

... Students will understand that 1) molecular mechanisms that preserve the fidelity of the genetic sequence have been favored by natural selection, 2) some entities, such as HIV, lack some of these mechanisms and so have a higher rate of mutation and evolution, and 3) many challenges posed to medical s ...
What is DNA Fingerprinting
What is DNA Fingerprinting

... 2. Go to the following site: http://www.pbs.org/wgbh/nova/sheppard/analyze.html Before doing the activity, read the following background information: Background Essay: Create a DNA Fingerprint In the last 15 years, DNA has played an increasingly important role in our legal system. Tissue evidence is ...
Types of Genetic Testing
Types of Genetic Testing

...  Diagnose > 100 disorders, cells analyzed for chromosomal and biochemical disorders  Risk of infection and spontaneous abortion  Normally only used when: ...
DNA
DNA

... Curing genetic diseases – 5% of babies in USA born with one Decoding the human genome (determine the nucleotide sequence of about 3 billion nucleotides or about100,000 genes and to map their location on every chromosome) Completed in June 2000 Personal Id Diagnosis of disease – 4,000 human genetic ...
DNA Powerpoint Notes
DNA Powerpoint Notes

... process occurs due to the enzyme ___________________ which also checks for ___________________ as it goes. ...
Name Living Environment Test 10 1. Evidence that best supports the
Name Living Environment Test 10 1. Evidence that best supports the

... 20. A restriction enzyme is used to cut the DNA from species A and B. The enzyme binds to the sequence G G G A T T and cuts between G and A. State how many cuts will be made in the DNA sequences of each species when this enzyme is used. [1] ...
Chapter 16 Review
Chapter 16 Review

... The DNA of somatic cells is constantly bombarded with agents from the environment that could cause mutations. Select the correct statement about mutations and somatic cells. A. Somatic cells are in the various organs of organisms and are shielded from the harmful agents that might cause mutations. ...
2421_Ch9.ppt
2421_Ch9.ppt

... RFLPs - restriction fragment length polymorphisms – Inherited differences in distance between restriction enzyme sites. Can test for inherited differences in a person’s DNA (can be used to test for genetic diseases -- genetic screening) ...
Genetics Outcomes
Genetics Outcomes

HOW SAGE WORKS (Reference http://www
HOW SAGE WORKS (Reference http://www

LEQ: How do we splice new genes into DNA?
LEQ: How do we splice new genes into DNA?

... Reverse Transcriptase used to make genes for cloning 1. Transcribe DNA into RNA in the ...
Establishment of a screening service for BM and UCMD
Establishment of a screening service for BM and UCMD

... demonstrates splice + large del/dup – Potential to reduce sequencing load • Genomic: 107 fragments • cDNA: 26 fragments ...
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Cell-free fetal DNA

Cell-free fetal DNA (cffDNA) is fetal DNA circulating freely in the maternal blood stream. It can be sampled by venipuncture on the mother. Analysis of cffDNA provides a method of non-invasive prenatal diagnosis.cffDNA originates from the trophoblasts making up the placenta. It is estimated that 2-6% of the DNA in the maternal blood is fetal in origin. The fetal DNA is fragmented and makes its way into the maternal bloodstream via shedding of the placental microparticles into the maternal bloodstream (figure 1). Studies have shown that cffDNA can first be observed as early as 7 weeks gestation, and the amount of cffDNA increases as the pregnancy progresses. cffDNA diminishes quickly after the birth of the baby, so that it is no longer detectable in the maternal blood approximately 2 hours after birth. cffDNA is significantly smaller than the maternal DNA in the bloodstream, with fragments approximately 200bp in size. Many protocols to extract the fetal DNA from the maternal plasma use its size to distinguish it from the maternal DNA.Studies have looked at, and some even optimized, protocols for testing non-compatible RhD factors, sex determination for X-linked genetic disorders and testing for single gene disorders. Current studies are now looking at determining aneuploidies in the developing fetus. These protocols can be done earlier than the current prenatal testing methods, and have no risk of spontaneous abortion, unlike current prenatal testing methods. Non-invasive prenatal diagnosis (NIPD) has been implemented in the UK and parts of the US; it has clear benefits above the standard tests of chorionic villi sample (CVS) and amniocentesis which have procedure-related miscarriage risks of about 1 in 100 pregnancies and 1 in 200 pregnancies, respectively.As a method of prenatal diagnosis, cell-free fetal DNA techniques share the same ethical and practical issues, such as the possibility of prenatal sex discernment and sex selection.
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