Pyromania USAFSAM “EPI Lab” MSgt Stephen Christian, USAF, MSgt, MT (ASCP) Lucinda Sinclair, GS-11 1 Distribution Statement A: Approved for Public release;

Slides:



Advertisements
Similar presentations
Pyrosequencing at LWH Carly Broadhurst.
Advertisements

MCB 317 Genetics and Genomics Topic 11, part 2 Genomics.
PCR way of copying specific DNA fragments from small sample DNA material "molecular photocopying" It’s fast, inexpensive and simple Polymerase Chain Reaction.
COMPUTER EXERCISE Design of PCR and PCR-RFLP experiments This presentation shows all steps of a PCR-RFLP experiment and is a companion of the computer.
SEQUENCING-related topics 1. chain-termination sequencing 2. the polymerase chain reaction (PCR) 3. cycle sequencing 4. large scale sequencing stefanie.hartmann.
DNA Sequencing.
Proprietary Bead Deposition Load DNA & Enzyme beads into PicoTiter™ Plate.
PCR Polymerase Chain Reaction. PCR - a method for amplifying (copying) small amount of DNA in nearly any amount required, starting with a small initial.
DNA Sequencing How do you do it?. DNA Sequencing DNA sequencing – used to determine the actual DNA sequence of an organism. Using a computer, one can.
Nucleotides and Nucleic Acids Part 2 (and a little bit from Chapter 9) Chapter 8.
Definition of PCR Requirements for PCR PCR Process Agarose gel electrophoresis.
Genomic DNA purification
Emily Buckhouse. Nitrogenous Bases Nucleosides  Base linked to a 2-deoxy-D-ribose at 1’ carbon Nucleotides Nucleosides with a phosphate at 5’ carbon.
Sequencing tutorial Peter HANTZ EMBL Heidelberg.
7.1 cont’d: Sanger Sequencing SBI4UP MRS. FRANKLIN.
The polymerase chain reaction (PCR) rapidly
NEXT GENERATION SEQUENCING Technologies on Biomedical Research
HIV GENOTYPE ASSAY Anabelia Perez, MLT (ASCP) Molecular Technologist August 6, 2008.
Bioinformatics/PCR Lab How does having a certain genetic marker affect chances of getting brain cancer?
Automated DNA Sequencing LECTURE 7: Biotechnology; 3 Credit hours Atta-ur-Rahman School of Applied Biosciences (ASAB) National University of Sciences and.
DNA Sequencing Today, laboratories routinely sequence the order of nucleotides in DNA. DNA sequencing is done to: Confirm the identity of genes isolated.
MCB 7200: Molecular Biology
1.) DNA Extraction Follow Kit Grind sample Mix with solution and spin Bind, Wash, Elute.
Recombinant DNA Technology……….. BTEC3301. DNA Libraries How do you identify the gene of interest and clone only the DNA sequence you are interested? Read.
Announcements Lab notebooks due Monday by 5 No Ch. 9 Part 2 homework
© 2005 Prentice Hall Inc. / A Pearson Education Company / Upper Saddle River, New Jersey Chapter 3 Fundamentals of Mapping and Sequencing Basic principles.
Chapter 14: DNA Amplification by Polymerase Chain Reaction.
Polymerase Chain Reaction PCR. PCR allows for amplification of a small piece of DNA. Some applications of PCR are in: –forensics (paternity testing, crimes)
DNA sequencing methods. Developing new methods and instruments that permit fast polynucleotide sequencing has attracted considerable attention recently.
Chapter 5: Exploring Genes and Genomes Copyright © 2007 by W. H. Freeman and Company Berg Tymoczko Stryer Biochemistry Sixth Edition.
Stratton Nature 45: 719, 2009 Evolution of DNA sequencing technologies to present day DNA SEQUENCING & ASSEMBLY.
Molecular Testing and Clinical Diagnosis
GENE SEQUENCING. INTRODUCTION CELL The cells contain the nucleus. The chromosomes are present within the nucleus.
Ultra-High Throughput DNA Sequencing on the 454/Roche GS-FLX
Sequencing by the Sanger Dideoxynucleotide Chain Termination Method 1. Prepare replication template denature, add synthetic primer, promote annealing TAGGCGA.
Sequencing tutorial Peter HANTZ EMBL Heidelberg.
Sanger or Dideoxy DNA Sequencing
Nucleic acid labeling Radioactive deoxynucleoside triphosphate (dNTP); labeled with H 3 (tritium) or P 32.dNTP Purposes: 1. keep tracking small amounts.
Biotechnology and Genetic Engineering PBIO 450/550 Characterization of DNA clones including: Restriction Enzyme (RE) mapping Subcloning Southerns Northerns*
PCR With PCR it is possible to amplify a single piece of DNA, or a very small number of pieces of DNA, over many cycles, generating millions of copies.
Genomics I: The Transcriptome RNA Expression Analysis Determining genomewide RNA expression levels.
DNA Sequencing Hunter Jones, Mitchell Gage. What’s the point? In a process similar to PCR, DNA sequencing uses a mixture of temperature changes, enzymes.
Polymerase Chain Reaction Chromosome 16: PV92Alu PCR TM.
CAMPBELL BIOLOGY Reece Urry Cain Wasserman Minorsky Jackson © 2014 Pearson Education, Inc. TENTH EDITION CAMPBELL BIOLOGY Reece Urry Cain Wasserman Minorsky.
Rajan sharma.  Polymerase chain reaction Is a in vitro method of enzymatic synthesis of specific DNA sequences.  This method was first time developed.
Metagenomics The study of metagenomes, genetic material recovered directly from environmental samples. Term: Coined in 1998 to refer to the idea that a.
I. PCR- Polymerase Chain Reaction A. A method to amplify a specific piece of DNA. DNA polymerase adds complementary strand DNA heated to separate strands.
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
6.3 – Manipulating genomes
Genetic Engineering.
Midterm Review Feb
PCR uses polymerases to copy DNA segments.
Sequencing Technologies
AMPLIFYING AND ANALYZING DNA.
SOLEXA aka: Sequencing by Synthesis
DNA Sequencing The DNA from the genome is chopped into bits- whole chromosomes are too large to deal with, so the DNA is broken into manageably-sized overlapping.
Sequencing and Copying DNA
Introduction to Bioinformatics II
A B - deoxynucleotide (dNTP) dideoxynucleotide (ddNTP)
PCR uses polymerases to copy DNA segments.
PCR uses polymerases to copy DNA segments.
Polymerase Chain Reaction (PCR) & DNA SEQUENCING
Introduction to Polymerase Chain Reaction (PCR)
PCR uses polymerases to copy DNA segments.
PCR uses polymerases to copy DNA segments.
PCR uses polymerases to copy DNA segments.
Standard (Sanger) sequencing
SBI4U0 Biotechnology.
Polymerase Chain Reaction (PCR) & DNA SEQUENCING
PCR uses polymerases to copy DNA segments.
Presentation transcript:

Pyromania USAFSAM “EPI Lab” MSgt Stephen Christian, USAF, MSgt, MT (ASCP) Lucinda Sinclair, GS-11 1 Distribution Statement A: Approved for Public release; distribution is unlimited. 311 ABG/PA No , 12 Mar 2010

Team Aerospace Begins Here! Overview Introduction to Influenza Why\What to Sequence Sequencing (Pyro versus Sanger) Pyrosequencing for influenza antiviral resistance markers (Tamiflu resistance in 2009 A (H1/N1) 2

Team Aerospace Begins Here! Influenza 3

Team Aerospace Begins Here! = H1N1 50,000,000 deaths 1957 = H2N2 1,000,000 deaths 1968 = H3N2 500,000 deaths Annual flu 250,000 deaths H5N1 annual Types of influenza 2009 A/H1N1 A,B, and C (Epidemics = A &B) Pandemics = A only

Team Aerospace Begins Here! Influenza Genome PB2 PB1 PA HA NP NA M NS 5

Team Aerospace Begins Here! HA1 region of HA gives the most bang for the buck. Why/What to Sequence PB2 PB1 PA HA NP NA M NS 13,588 bp’s 6 Amantadine Presence/Absence of Antiviral resistance markers Tamiflu

Team Aerospace Begins Here! Nucleic Acid Extraction Traditional RT PCR Sequencing 7 Sequencing (Pyro versus Sanger)

Team Aerospace Begins Here! Sanger Sequencing Sequencing by Chain Termination Extract Nucleic Acid Produce amplicon Clean Amplicon Big Dye Rxn (Chain Termination) Clean Big Dye Rxn Electrophoresis of Big Dye (Sequencer) Analyze Sequence Data 8

Team Aerospace Begins Here! Produce Amplicon (HA1) Template (Amplicon) 9

Team Aerospace Begins Here! Clean Amplicon (HA1) 10 Template (Amplicon) Clean PCR Product Amplicon (dATP’s) (dGTP’s) (dCTP’s) (dTTP’s) Polymerase Salts Buffers

Team Aerospace Begins Here! Template (Amplicon) Primer dNTP’s A (dATP’s) G(dGTP’s) C (dCTP’s) T (dTTP’s) ddNTP’s A G C T Big Dye Reaction

Team Aerospace Begins Here! Big Dye Reaction 12 Template (Amplicon)

Team Aerospace Begins Here! Clean Big Dye Reaction 13

Team Aerospace Begins Here! Electrophoresis 14

Team Aerospace Begins Here! Results from Electrophoresis 15

Team Aerospace Begins Here! Sequence Analysis Build Single Contig Analyze constructed nucleotide sequence (Protein) Relate to current vaccine strain on phylogenetic tree 16

Team Aerospace Begins Here!Pyrosequencing 17 Sequencing by Addition Extract Nucleic Acid Produce amplicon Pyrosequencer

Team Aerospace Begins Here!Pyrosequencing

2. Immobilize biotinylated PCR products onto streptavidin-coated beads 3. Separate strands by denaturation in NaOH 5. Anneal sequencing primer 96 samples are processed in parallel 4. Wash /neutralize the immobilized strand 1. Amplify relevant region by PCR ( bp), using 1 biotinylated primer Simple Sample Preparation

Team Aerospace Begins Here! 1.) Hybridize sequence primer along with DNA polymerase, ATP sulfurylase, luciferase, apyrase, adenosine 5’ phosphosuflate (APS) and luciferin. Polymerase Apyrase sulfurylase luciferase APS luciferin PolymerasePyrosequencing

Team Aerospace Begins Here! dNTP’s added one at a time Apyrase sulfurylase luciferase APS luciferin Polymerase 2.) Add one of four dNTP’s, DNA polymerase incorporates dNTP’s (if it is complementary) releasing PPi.Pyrosequencing

Team Aerospace Begins Here! Apyrase sulfurylase luciferase APS luciferin Polymerase 2.) Add one of four dNTP’s, DNA polymerase incorporates dNTP’s (if it is complementary) releasing PPi.Pyrosequencing

Team Aerospace Begins Here! Apyrase sulfurylase luciferase APS luciferin Polymerase 2.) Add one of four dNTP’s, DNA polymerase incorporates dNTP’s (if it is complementary) releasing PPi. PPiPyrosequencing

Team Aerospace Begins Here! Apyrase sulfurylase luciferase APS luciferin Polymerase ATP sulfurylase converts PPi and APS to ATP. Luciferase converts luciferin and ATP to oxyluciferin which generates light read by a camera. + PPi = ATPPyrosequencing

Team Aerospace Begins Here! Apyrase sulfurylase luciferase APS luciferin Polymerase ATP sulfurylase converts PPi and APS to ATP. Luciferase converts luciferin and ATP to oxyluciferin which generates light read by a camera. + PPi = ATP oxyluciferinPyrosequencing

Team Aerospace Begins Here! Hybridize sequence primer, DNA polymerase, ATP sulfurylase, luciferase, apyrase, adenosine 5’ phosphosuflate (APS) and luciferin. Add one of four dNTP’s, DNA polymerase incorporates dNTP’s (if it is complementary) releasing PPi. ATP sulfurylase converts PPi and APS to ATP. Luciferase converts luciferin and ATP to oxyluciferin which generates light read by a camera. Apyrase degrades dNTP’s and ATP, when complete next dNTP is added. As process continues, the correct DNA sequence is built up and displayed.Pyrosequencing

Team Aerospace Begins Here! 27

Team Aerospace Begins Here! 5Sanger sequencing steps VS. 2 Pyrosequencing steps

Team Aerospace Begins Here! Neuraminidase Pyrosequencing 29

Team Aerospace Begins Here! 30 Questions