By Michael Fraczek and Caden Boyer

Slides:



Advertisements
Similar presentations
Lecture 41 Prof Duncan Shaw. Genetic Variation Already know that genes have different alleles - how do these arise? Process of mutation - an alteration/change.
Advertisements

Lecture 2 Strachan and Read Chapter 13
Applications of genome sequencing projects 1) Molecular Medicine 2) Energy sources and environmental applications 3) Risk assessment 4) Bioarchaeology,
applications of genome sequencing projects
SC.912.L.16.4 Explain how mutations in the DNA sequence may or may not result in phenotypic change. Explain how mutations in gametes may result in.
CS177 Lecture 9 SNPs and Human Genetic Variation Tom Madej
Chromosomes carry genetic information
Single nucleotide polymorphisms and applications Usman Roshan BNFO 601.
Mutations Section 12–4 This section describes and compares gene mutations and chromosomal mutations.
Changes in DNA can produce variation
Analyzing DNA Differences PHAR 308 March 2009 Dr. Tim Bloom.
Last lesson we looked at: What is the definition of a gene?
Doug Brutlag 2011 Genomics & Medicine Doug Brutlag Professor Emeritus of Biochemistry &
SNPs Daniel Fernandez Alejandro Quiroz Zárate. A SNP is defined as a single base change in a DNA sequence that occurs in a significant proportion (more.
Allele. Alternate form of a gene gene variant autosome.
CS177 Lecture 10 SNPs and Human Genetic Variation
SNP Haplotypes as Diagnostic Markers Shrish Tiwari CCMB, Hyderabad.
A gene is a particular sequence (a string) of nucleotides on a particular site of a chromosome. It is made up of combinations of A, T, C, and G. These.
Do Now: 1) How do somatic and sex cell mutations differ. 2) A mutation causes the adenine in the following sequence to be changed to a guanine. How does.
Unit 4, Topic 5 - Genetic Engineering
Julia N. Chapman, Alia Kamal, Archith Ramkumar, Owen L. Astrachan Duke University, Genome Revolution Focus, Department of Computer Science Sources
Chapter 12 Assessment How could manipulating DNA be beneficial?
Chapter 21 Genetic Variation and Evolution. What is the goal of the Fast Plant Experiment? What are you measuring? What are you comparing?
MUTATIONS _______________ are changes in the genetic material. MUTATIONS mistakes REMEMBER! Mutations can happen when cells make _____________ in.
MUTATIONS. Mutations are heritable changes in genetic information Only mutation in the GAMETES can be passed on from generation to generation There can.
Unit 1 – Living Cells.  The study of the human genome  - involves sequencing DNA nucleotides  - and relating this to gene functions  In 2003, the.
Notes: Human Genome (Right side page)
Genetics 3.1 Genes. Essential Idea: Every living organism inherits a blueprint for life from its parents.
Different microarray applications Rita Holdhus Introduction to microarrays September 2010 microarray.no Aim of lecture: To get some basic knowledge about.
Reality Science Fiction! Just silly.. 1. Some mutations affect a single gene, while others affect an entire chromosome. 2. A mutation is a change in an.
MS-LS 3-1. I will explain how mutations can effect organisms in positive, negative, and neutral ways.
8.7 Mutations A mutation is a change in an organism’s DNA. May occur during replication. May affect a single gene, or an entire chromosome May or may not.
SC.912.L.16.3 DNA Replication. – During DNA replication, a double-stranded DNA molecule divides into two single strands. New nucleotides bond to each.
Single Nucleotide Polymorphisms (SNPs
Karyotyping Cancer.
The Function of DNA.
Mutations Bio Explain how mutations in DNA that result from interactions with the environment (i.e. radiation and chemicals) or new combinations.
The ABC’s of DNA Barry Bowman.
DNA Marker Lecture 10 BY Ms. Shumaila Azam
A mutation is a change in an organism’s DNA.
Mutations Bio Explain how mutations in DNA that result from interactions with the environment (i.e. radiation and chemicals) or new combinations.
School of Pharmacy, University of Nizwa
12- 4 Mutations.
breast cancer 2, early onsetpro What does this protein make up or do?
LIFE SCIENCE 7TH GRADE CHAPTER 5 LESSON 1 THE GENETIC CODE
Mutations change in the DNA or RNA sequence May result in new alleles
What makes a mutant?.
ABO Blood Type: An Example of Genetic Variation
Heredity Lesson 8.
Relationship between Genotype and Phenotype
Mutations and Genetic Abnormalities
Mutations changes in the DNA sequence that can be inherited
A mutation is a change in an organism’s DNA.
Genomic alterations in breast cancer cell line MDA-MB-231.
Some mutations affect a single gene, while others affect an entire chromosome.
“TaqMan genotyping Assay’’
MUTATIONS.
Relationship between Genotype and Phenotype
By Stitziel, Tseng, Pervouchine, Goddeau, Kasif, Liang
A ____________ is a change in an organism’s DNA.
How will cancer be treated in the 21st century?
A mutation is a change in an organism’s DNA.
School of Pharmacy, University of Nizwa
SC.912.L.16.4 Explain how mutations in the DNA sequence may or may not result in phenotypic change. Explain how mutations in gametes may result in.
Copyright Pearson Prentice Hall
Specific Tumor Suppressor Genes
Reminder The AP Exam registration is open in Naviance. The Exam is on Monday, May 13. I’ll let you know when the next test/homework will be.
SNPs and CNPs By: David Wendel.
Presentation transcript:

By Michael Fraczek and Caden Boyer SNPs By Michael Fraczek and Caden Boyer

What is it? The Video “Single Nucleotide Polymorphisms” or SNPs Single nucleotide change in genetic code To be “SNPs”, 2 or more versions of genetic differences present in 1% of population Each “SNP” site has 4 possible versions (A, C, G & T) Occur roughly every 300 nucleotides; 10 million SNPs total present in human genome

Basic Mechanics Two main types of SNPs: Linked SNPs and Causative SNPs Linked SNPs do not affect protein production Still affects drug and environmental responses Two types of Causative SNPs: Non-coding and Coding Coding SNPs change amino acid sequences Non-coding SNPs change the timing or location of proteins “Haplotype” - a combination of SNPs found on alleles in a region of DNA that are inherited from each parent

Applications? SNPs Profile for Drug Effectiveness SNP microarrays for Cancer Research Risk assessment of cancer cells Investigating allelic association of cancers Identification of cancer predisposition and tumor suppressor genes, as well as oncogenes Use as a biological marker Plant genotyping Pacific Salmon Determining response to environmental factors Identifying harmful mutations Risk assessment - genome copy number changes in cancer cells, etc. Plant genotyping - SNPs found in maize Environmental factors - determining individual response to environmental factors like toxins

Article - Alaska Department of Fish and Game The Article

Sources https://ghr.nlm.nih.gov/primer/genomicresearch/snp http://learn.genetics.utah.edu/content/precision/snips/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430687/ https://www.adfg.alaska.gov/static/fishing/PDFs/research/geneconservation/snp/sm ith.pdf http://www.cabi.org/cabebooks/ebook/20083014993 https://www.23andme.com/gen101/snps/ http://www.dnatube.com/video/226/Single-Nucleotide-Polymorphisms-SNPs http://www.dnatube.com/video/2885/Testing-polymorphism-microarray-method

Explaining Video If no flash player: 2nd Video Or: 3rd Video