Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels.

Slides:



Advertisements
Similar presentations
Vanderbilt Center for Quantitative Sciences Summer Institute Sequencing Analysis Yan Guo.
Advertisements

MCB 317 Genetics and Genomics Topic 11, part 2 Genomics.
High-Throughput Sequencing Technologies
Recombinant DNA technology
RNA-Seq An alternative to microarray. Steps Grow cells or isolate tissue (brain, liver, muscle) Isolate total RNA Isolate mRNA from total RNA (poly.
Next-generation sequencing and PBRC. Next Generation Sequencer Applications DeNovo Sequencing Resequencing, Comparative Genomics Global SNP Analysis Gene.
DNA Sequencing.
DNA Sequencing and Gene Analysis
RNA-Seq An alternative to microarray. Steps Grow cells or isolate tissue (brain, liver, muscle) Isolate total RNA Isolate mRNA from total RNA (poly.
Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels.
Chapter 10 DNA Sequencing.
Emily Buckhouse. Nitrogenous Bases Nucleosides  Base linked to a 2-deoxy-D-ribose at 1’ carbon Nucleotides Nucleosides with a phosphate at 5’ carbon.
7.1 cont’d: Sanger Sequencing SBI4UP MRS. FRANKLIN.
with an emphasis on DNA microarrays
MCB 7200: Molecular Biology
Lecture 189Functional Genomics Based on chapter 8 Functional and Comparative Genomics Copyright © 2010 Pearson Education Inc.
HC70AL Spring 2009 Gene Discovery Laboratory RNA and Tools For Studying Differential Gene Expression During Seed Development 4/20/09tratorp.
Affymetrix vs. glass slide based arrays
Analyzing your clone 1) FISH 2) “Restriction mapping” 3) Southern analysis : DNA 4) Northern analysis: RNA tells size tells which tissues or conditions.
Plant Molecular Systematics Michael G. Simpson
 It is the methods scientist use to study and manipulate DNA.  It made it possible for researchers to genetically alter organisms to give them more.
-The methods section of the course covers chapters 21 and 22, not chapters 20 and 21 -Paper discussion on Tuesday - assignment due at the start of class.
Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels.
DNA MICROARRAYS WHAT ARE THEY? BEFORE WE ANSWER THAT FIRST TAKE 1 MIN TO WRITE DOWN WHAT YOU KNOW ABOUT GENE EXPRESSION THEN SHARE YOUR THOUGHTS IN GROUPS.
Announcements Lab notebooks due Monday by 5 No Ch. 9 Part 2 homework
Microarray Technology
 It is the methods scientist use to study and manipulate DNA.  It made it possible for researchers to genetically alter organisms to give them more.
© 2005 Prentice Hall Inc. / A Pearson Education Company / Upper Saddle River, New Jersey Chapter 3 Fundamentals of Mapping and Sequencing Basic principles.
Pyromania USAFSAM “EPI Lab” MSgt Stephen Christian, USAF, MSgt, MT (ASCP) Lucinda Sinclair, GS-11 1 Distribution Statement A: Approved for Public release;
UNIT 1 INFORMATION METHODS OF A CELL. What do you know about DNA? Building blocks are called? –nucleotides The shape is ? –Double helix The three primary.
RNA and PROTEIN SYNTHESIS Chapter 13-1 & 13-2
13-1 Changing the Living World
Genomics: READING genome sequences ASSEMBLY of the sequence ANNOTATION of the sequence carry out dideoxy sequencing connect seqs. to make whole chromosomes.
Molecular Biology Dr. Chaim Wachtel May 28, 2015.
Genomics I: The Transcriptome
Polymerase Chain Reaction (PCR)
Gene expression. The information encoded in a gene is converted into a protein  The genetic information is made available to the cell Phases of gene.
Sequencing DNA 1. Maxam & Gilbert's method (chemical cleavage) 2. Fred Sanger's method (dideoxy method) 3. AUTOMATED sequencing (dideoxy, using fluorescent.
Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels.
Gene, MicroArray and GAs Ashish Anand Kanpur Genetic Algorithms Laboratory (KanGAL) IIT Kanpur.
Chapter 20: DNA Technology and Genomics - Lots of different techniques - Many used in combination with each other - Uses information from every chapter.
Lecture 23 – Functional Genomics I Based on chapter 8 Functional and Comparative Genomics Copyright © 2010 Pearson Education Inc.
Molecular Genetic Technologies Gel Electrophoresis PCR Restriction & ligation Enzymes Recombinant plasmids and transformation DNA microarrays DNA profiling.
Gene expression and DNA microarrays No lab on Thursday. No class on Tuesday or Thursday next week –NCBI training Monday and Tuesday –Feb. 5 during class.
Sanger or Dideoxy DNA Sequencing
Biotechnology and Genetic Engineering PBIO 450/550 Characterization of DNA clones including: Restriction Enzyme (RE) mapping Subcloning Southerns Northerns*
DNA Microarray Overview and Application. Table of Contents Section One : Introduction Section Two : Microarray Technique Section Three : Types of DNA.
Semiconservative DNA replication Each strand of DNA acts as a template for synthesis of a new strand Daughter DNA contains one parental and one newly synthesized.
Lecture 26 GWAS Based on chapter 9 Functional and Comparative Genomics Copyright © 2010 Pearson Education Inc.
Higher Human Biology Unit 1 Human Cells KEY AREA 5: Human Genomics.
Human Genomics Higher Human Biology. Learning Intentions Explain what is meant by human genomics State that bioinformatics can be used to identify DNA.
Microarray: An Introduction
Green with envy?? Jelly fish “GFP” Transformed vertebrates.
TRANSCRIPTION (DNA → mRNA). Fig. 17-7a-2 Promoter Transcription unit DNA Start point RNA polymerase Initiation RNA transcript 5 5 Unwound.
© 2005 Prentice Hall Inc. / A Pearson Education Company / Upper Saddle River, New Jersey Chapter 5 RNA Expression Analysis Determining genomewide.
6.3 – Manipulating genomes
Next generation sequencing
PCR Optimization To optimize PCR the following must be evaluated and fine tuned Target DNA Too small or too large Good or poor quality Complete or incomplete.
Microbial Genomes and techniques for studying them.
Chapter 20: DNA Technology and Genomics
SOLEXA aka: Sequencing by Synthesis
Screening a Library for Clones Carrying a Gene of Interest
DNA Technology.
CHAPTER 12 DNA Technology and the Human Genome
The transcription process is similar to replication.
High-Throughput Sequencing Technologies
High-Throughput Sequencing Technologies
Chapter 20: DNA Technology and Genomics
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
Using the DNA Sequence Knowing the sequence of an organism’s DNA allows researchers to study specific genes, to compare them with the genes of other organisms,
Presentation transcript:

Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels

Genomic analysis of gene expression Methods capable of giving a “snapshot” of RNA expression of all genes Can be used as diagnostic profile –Example: cancer diagnosis Can show how RNA levels change during development, after exposure to stimulus, during cell cycle, etc. Provides large amounts of data Can help us start to understand how whole systems function

Basics of microarrays DNA attached to solid support –Glass, plastic, or nylon RNA is labeled –Usually indirectly Bound DNA is the probe –Labeled RNA is the “target”

Cell-cycle regulated genes Each gene is a line on the longitudinal axis Treatments in different panels Cell-cycle stages are color coded at top Vertical axis groups genes by stage in which expression peaks Brown and Botstein, 1999 Alphacdc15cdc28Elu M/G1 G1 S G2 M

Analysis of microarray results Inherent variability: need for repetition –Biological and technical replicates Analysis algorithms –Based on statistical models Means of generating hypotheses that need to be tested

RNA- seq High throughput sequencing of cDNAs from biological samples Determine abundance of mRNA by representation in sequencing reads May detect variants (alternative splicing, specific alleles, etc.)

The structure of 2 ’,3 ’ -dideoxynucleotides Dideoxy Sequencing- The Old Way

The dideoxy sequencing method Figure 20-16a

© 2005 Prentice Hall Inc. / A Pearson Education Company / Upper Saddle River, New Jersey Summary of chain termination sequencing

Comparison of NextGen Sequencing Platforms

Pyrosequencing I (454 Strategy) Based on production of pyrophosphate during sequencing reaction Each time polymerase adds nucleotide (dNTP) to the growing strand, pyrophosphate (PPi) is released –Amount released equal to number of nucleotides added

Pyrosequencing II To quantitate amount of PPi released: –ATP sulfurylase converts PPi to ATP –ATP used by enzyme luciferase to produce light from the substrate luciferin The amount of light produced is directly proportional to the amount of ATP, which is proportional to the amount of PPi released

Pyrosequencing III Sequential addition of each dNTP gives sequence Apyrase enzyme used to degrade dNTPs after reaction completed Sequence read from amount of light emitted as each dNTP is added Nucleotide sequence Nucleotide added

Transcriptome Analysis by Pyrosequencing Like SAGE in that portions of each RNA are sequenced; abundance proportional to representation in sequencing “Micro reaction chambers” formed using emulsion of oil and aqueous phases to separate clones Sequencing strategy different from standard methodology; allows analysis of thousands of clones on one slide science.com/publications/multimedia/genome_sequencer/amplicon_07/wbt.htm science.com/publications/multimedia/genome_sequencer/amplicon_07/wbt.htm

Illumina Solexa Strategy -YouTube animation

-Can generate density of 10 7 clusters/cm 2

SOLiD Sequencing Strategy ABI site

Ion Torrent Sequencing Strategy -YouTube animation-YouTube animation chemistry