Different microarray applications Rita Holdhus Introduction to microarrays September 2010 microarray.no Aim of lecture: To get some basic knowledge about.

Slides:



Advertisements
Similar presentations
Linkage and Genetic Mapping
Advertisements

Lecture 2 Strachan and Read Chapter 13
CZ5225 Methods in Computational Biology Lecture 9: Pharmacogenetics and individual variation of drug response CZ5225 Methods in Computational Biology.
Introduction to genomes & genome browsers
Genetic Analysis in Human Disease
Recombinant DNA technology
Polymorphisms: Clinical Implications By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of Medicine, KSU.
MiRNA-drug resistance mechanisms Summary Hypothesis: The interplay between miRNAs, signaling pathways and epigenetic and genetic alterations are responsible.
Genetics and Health Jennifer Eyvindson Epi 6181 November 2006.
CS177 Lecture 9 SNPs and Human Genetic Variation Tom Madej
Positional Cloning LOD Sib pairs Chromosome Region Association Study Genetics Genomics Physical Mapping/ Sequencing Candidate Gene Selection/ Polymorphism.
Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.
Restriction Fragment Length Polymorphisms (RFLPs) By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of.
Identification of obesity-associated intergenic long noncoding RNAs
Paola CASTAGNOLI Maria FOTI Microarrays. Applicazioni nella genomica funzionale e nel genotyping DIPARTIMENTO DI BIOTECNOLOGIE E BIOSCIENZE.
CH 11 pg217 Role of Gene Expression DNA on several chromosomes –Only some of these genes are expressed at any given time Activation of a gene that results.
Large-Scale Copy Number Polymorphism in the Human Genome J. Sebat et al. Science, 305:525 Luana Ávila MedG 505 Feb. 24 th /24.
Genetic Analysis in Human Disease. Learning Objectives Describe the differences between a linkage analysis and an association analysis Identify potentially.
Control of Gene Expression Eukaryotes. Eukaryotic Gene Expression Some genes are expressed in all cells all the time. These so-called housekeeping genes.
CHAPTER 18 Molecular Biology and Medicine
Epigenome 1. 2 Background: GWAS Genome-Wide Association Studies 3.
The virochip (UCSF) is a spotted microarray. Hybridization of a clinical RNA (cDNA) sample can identify specific viral expression.
Analyzing DNA Differences PHAR 308 March 2009 Dr. Tim Bloom.
Computational research for medical discovery at Boston College Biology Gabor T. Marth Boston College Department of Biology
Finish up array applications Move on to proteomics Protein microarrays.
Next Generation Sequencing and its data analysis challenges Background Alignment and Assembly Applications Genome Epigenome Transcriptome.
Microarrays and Their Uses Brad Windle, Ph.D
CS177 Lecture 10 SNPs and Human Genetic Variation
A Genome-wide association study of Copy number variation in schizophrenia Andrés Ingason CNS Division, deCODE Genetics. Research Institute of Biological.
Michael Cummings David Reisman University of South Carolina Gene Regulation Part 2 Chapter 9.
Eukaryotic Genomes  The Organization and Control of Eukaryotic Genomes.
ABC for the AEA Basic biological concepts for genetic epidemiology Martin Kennedy Department of Pathology Christchurch School of Medicine.
Lecture 6. Functional Genomics: DNA microarrays and re-sequencing individual genomes by hybridization.
MEME homework: probability of finding GAGTCA at a given position in the yeast genome, based on a background model of A = 0.3, T = 0.3, G = 0.2, C = 0.2.
Recombination breakpoints Family Inheritance Me vs. my brother My dad (my Y)Mom’s dad (uncle’s Y) Human ancestry Disease risk Genomics: Regions  mechanisms.
Pathways between Genes and Behaviour. Functional Genomics Understanding the pathways between genes and behaviours (i.e., mechanisms of genes affecting.
Lecture 28 Genetics of Cancer Copyright © 2010 Pearson Education Inc.
ANALYSIS OF GENE EXPRESSION DATA. Gene expression data is a high-throughput data type (like DNA and protein sequences) that requires bioinformatic pattern.
Advances in Genetic Technology Class Notes Make sure you study this along with our first PowerPoint on Transgenics and your class Article notes.
Trends Biomedical Science
Genomics A Systematic Study of the Locations, Functions and Interactions of Many Genes at Once.
PLANT BIOTECHNOLOGY & GENETIC ENGINEERING (3 CREDIT HOURS) LECTURE 13 ANALYSIS OF THE TRANSCRIPTOME.
Transcriptome What is it - genome wide transcript abundance How do you obtain it - Arrays + MPSS What do you do with it when you have it - ?
Genomics A Systematic Study of the Locations, Functions and Interactions of Many Genes at Once.
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)
Human Genomics Higher Human Biology. Learning Intentions Explain what is meant by human genomics State that bioinformatics can be used to identify DNA.
1 From Bi 150 Lecture 0 October 4, 2012 An introduction to molecular biology... but you will learn the cell biology in this course.
Enhancers and 3D genomics Noam Bar RESEARCH METHODS IN COMPUTATIONAL BIOLOGY.
1 Finding disease genes: A challenge for Medicine, Mathematics and Computer Science Andrew Collins, Professor of Genetic Epidemiology and Bioinformatics.
Molecular Biology of Cancer AND Cancer Informatics (omics) David Boone.
Gene Expression Profiling Brad Windle, Ph.D
Looking Within Human Genome King abdulaziz university Dr. Nisreen R Tashkandy GENOMICS ; THE PIG PICTURE.
Epigenetics of cancer Vilja ja Mia.
High-throughput data used in bioinformatics
Chapter 2. Differential gene expression in Development
GENETIC BIOMARKERS.
Genomics A Systematic Study of the Locations, Functions and Interactions of Many Genes at Once.
Regulation of Gene Expression
Introduction to bioinformatics lecture 11 SNP by Ms.Shumaila Azam
What makes a mutant?.
Cell Signaling.
By Michael Fraczek and Caden Boyer
Chapter 18: Regulation of Gene Expression
Regulation of Gene Expression
Regulation of Gene Expression
Review Warm-Up What is the Central Dogma?
In these studies, expression levels are viewed as quantitative traits, and gene expression phenotypes are mapped to particular genomic loci by combining.
Review Warm-Up What is the Central Dogma?
Review Warm-Up What is the Central Dogma?
Presentation transcript:

Different microarray applications Rita Holdhus Introduction to microarrays September 2010 microarray.no Aim of lecture: To get some basic knowledge about the different applications microarrays are used for

microarray.no Systems biology – microarray applications The understanding of a biological system requires knowledge of the molecular mechanisms involved in regulation at: RNA level DNA level Gene expression miRNA expression DNA Copy Number SNP Protein level chIP on chip Protein arrays

microarray.no Gene expression Measuring: RNA in order to find gene expression changes Measuring RNA transcipts in order to determine the gene expression profile in the sample.

microarray.no Gene expression studies Gene affected by a given treatment Time series (with and without a given treatment) Patterns of gene activity (healthy vs. control) Predicting disease by gene patterns –Predict outcome of AML disease –MammaPrint (breast cancer prognosis)

microarray.no miRNA miRNA are small non-coding RNAs (19-23 nucleotides) miRNA act as regulators that binds to complementary sequences in the 3’UTR of a target mRNA trasncript > 800 human miRNA-encoding genes Regulate expression of least onethird of all human genes. Measuring: RNA in order to determine miRNA expression profiles

microarray.no miRNA study miRNA study of differentiated and dedefferentiated sarcomas Heatmap of differentially expressed miRNA betwwen the two sarcoma types

microarray.no miRNA miRNA have shown to be Critical in the development of organism Differentially expressed in tissues Involved in viral infection processes Associated with oncogenes Potential in miRNA expression profiling Insight in gene regulation mechanisms Biological subgrouping (diagnosis and prognosis) Identification of potential therapeutic miRNA targets

microarray.no DNA copy number DNA copy number changes in the genome are deletions (loss) and duplications (gain) Measuring: DNA in order to find DNA copy number changes duplication deletion

microarray.no DNA copy number Potential in DNA copy number profiling Identification of candidate (disease) genes Identification of genetic disorders/syndromes Lybæk et al., clin Genet 2008

microarray.no SNP SNPs are normally occuring DNA variants (markers) located in the genome SNPs are DNA sequence variations occuring when a single nucleotide –A, T, C or G in the genome differs between members of a species (or between paired chromosomes in an individual) SNP-genotyping is used to study diseases since SNP are inheritable. Genotyping is used for identifying novel candidate (disease) genes and mapping multifactorial conditions/diseases Measuring: DNA in order to determine the SNP-genotype profile

microarray.no SNP – linkage studies Linkage study is a method that allows us to determine regions of chromosomes that are likely to contain a risk gene, and rule out areas where there is a low chance of finding a risk gene The linkage method works by linking a given SNP-genotype to a given disease and thereby to a DNA region containing the disease causing gene. Patients needs to be related to each other.

microarray.no SNP - Linkage study Linkage study identified the gene causing Cold-Induced Sweating Syndrome (CISS) CISS is a very rare disease and has only been detected in 8 individuals from 5 different families Nan-Therese inherited the same mutated gene-allele from both here parents Knappskog et al., AM J Hum Genet 2003

microarray.no SNP – Association studies Association study: The same as linkage (linking a disease to a DNA region with a gene/genes), but samples are not related Association studies are used to so-called ”common public health diseases” as: –Diabetes –Rheumatism –Heart-/stroke diseases –Psychological diseases Such diseases are ”multifactorial” i.e influenced by both genetic- and environmental factors. Therefore association studies requires thousands of patients with a certain disease and thousands of control samples

microarray.no Association studies SNP-genotyping of genes involved in development of schizophrenia –4 718 persons with schizophrenia – control persons –Individuals included from 10 countries The deletions were times more frequent in persons with schizophrenia than in control persons Indicates that the genes located in these deletions are involved in development of schizophrenia

microarray.no chIP-on-chip chIP-on-chip: chromatin immunoprecipitation-on-chip Immunoprecipitation of DNA-binding proteins and their target DNA sequences Regulatory proteins binds to promotor DNA regions and therby regulate gene expression Measuring: DNA fragments that has been bound to a specific protein

microarray.no chIP-on-chip Potential in chIP profiling Insight into transciptional regulation and epigenomic events Information of mechanisms involved in cell proliferating, cell fate determination, oncogenesis, apoptosis and gene silencing. Study of transcription factors and gene expression in human embryonic stem cells vs. in differentiated tissues and cell types Identification of target genes for three stem cell specific transcription factors

microarray.no Protein arrays Screening of thousands of different interactions: –Protein - antibody –Protein – protein –Protein – ligand –Protein – drug –Enzyme – substrate Different types of protein arrays: –Funcational arrays – e.g kinase arrays –Capture array – antobodies

microarray.no Systems biology – microarray applications Transciptome mRNA expression miRNA expression Splice variance Genome structure DNA copy number Genome variation Single nucleotide polymorphism Copy number variations Proteome Protein-protein interactions DNA-protein interaction Epigenetics DNA Methylation Chromatin structure