1 100 120 University of Oklahoma Genome Center4/14/12.

Slides:



Advertisements
Similar presentations
RAPD Randomly Amplified Polymorphic DNA
Advertisements

Molecular cloning overview Steps to prepare vector hour overnight culture 2.Minipreps (day immediately following O/N) (use Qiaprep spin miniprep.
SEPARATION OF DNA FRAGMENTS BY LENGTH. Organic molecules such as DNA are charged. DNA is negatively charged because the phosphates (red circles) that.
The 454 and Ion PGM at the Genomics Core Facility Dr. Deborah Grove, Director for Genetic Analysis Genomics Core Facility Huck Institutes of the Life Sciences.
PCR Basics Purpose of PCR Overview Components of PCR Reaction
PCR Basics 1.Purpose of PCR 2.Overview 3.Components of PCR Reaction 4.Variables Temperature Cycle Times and Numbers Primer Buffer Polymerase 5.Experimental.
Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome Jay Shendure, Gregory J. Porreca, Nikos B. Reppas, Xiaoxia Lin, John P. McCutcheon.
The SOLiD System: Next-Generation Sequencing Overview of the SOLiD System –  Scalable  Accurate Ultra High Throughput  Flexible  Mate Pairs.
Update on Next-Generation Sequencing
Competitive multiplex-PCR Amplicon Sequencing Library Preparation Note: Load into slide show mode, and click mouse periodically to play animation show.
PCR Primer Design Guidelines
-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.
CUGI Pilot Sequencing/Assembly Projects Christopher Saski.
Sequencing at the speed of life. Simple is beautiful.
Detection of Genomic Rearrangements in K562 cells using Paired End Sequencing Rosa Maria Alvarez Massachusetts Institute of Technology Class of 2009.
PCR Forensics. Today’s Lab There has been an outbreak of Salmonella poisoning in the Student Union cafeteria at Stanford University cafeteria. You have.
Polymerase Chain Reaction (PCR) Developed in 1983 by Kary Mullis Major breakthrough in Molecular Biology Allows for the amplification of specific DNA fragments.
Stratton Nature 45: 719, 2009 Evolution of DNA sequencing technologies to present day DNA SEQUENCING & ASSEMBLY.
Chapter 08 Author: Kelly Elkins © 2013 Elsevier, Inc. All rights reserved.
1. 2 VARIANTS OF PCR APPLICATIONS OF PCR MECHANICS OF PCR WHAT IS PCR? PRIMER DESIGN.
© 2005 Prentice Hall Inc. / A Pearson Education Company / Upper Saddle River, New Jersey Progress in genome sequencing  Human Genome Project  10.
Ultra-High Throughput DNA Sequencing on the 454/Roche GS-FLX
How many cycles you are going to run? Sequencing with transposons vs. traditional sequencing TGS Methodology 1. Perform transposition reaction 2. Transform,
Comparison between old generation and new generation of sequencing machines.
Polymerase Chain Reaction (PCR) Used to amplify a sample of DNA Many applications, including: DNA sequencing Phylogeny Diagnosis of genetic disorders Identity.
Polymerase Chain Reaction What is PCR History of PCR How PCR works Optimizing PCR Fidelity, errors & cloning PCR primer design Application of PCR.
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.
Introduction to PCR Polymerase Chain Reaction
Supplemental Figure 1. HD CAG repeat lengths and their corresponding melting temperatures in a Caucasian population. For each sample, top half of each.
Primers to map bsd deletion points on genomic DNA NameForwardReverse Amplicon size (base pairs) A15’-CCACGGATGGAGTGAGTTCT-3’5’-GCCCCCAAGATGAGGATTAT-3’931.
Presented by Samuel Chapman. Pyrosequencing-Intro The core idea behind pyrosequencing is that it utilizes the process of complementary DNA extension on.
Library QA & QC Day 1, Video 3
HRM Assay and Optimization 1. DNA Quality 2. Amplicon LengthAmplicon  lengths of 100–300 bp 3. Primer Selection 4. Dye Selection 5. MgCl2 Concentration.
Assay I HLA-DQ Alpha (A1) Haplotype. Purpose To determine which one of several known alleles is present at the HLA DQ α locus on each of an individual’s.
16S rRNA Experimental Design
Introduction to PCR Polymerase Chain Reaction
Polymerase Chain Reaction
Figure S1. Boxplot shows distribution of pre-processed DNA methylation level (β values) from all the samples and different groups used for comparison.
Restriction Enzyme Digestion of Phage DNA
PCR Basics Purpose of PCR Overview Components of PCR Reaction
DNA Sequencing -sayed Mohammad Amin Nourion -A’Kia Buford
Overview Wednesday Thursday Labs 12, 13 & 14 due March 7th
Manlio Fusciello Jaakko Itkonen Maarja Laos Tania Quirin
RNA molecule RNA fragment Activity Intro Slide:
Primer design.
Polymerase Chain Reaction
California Department of Justice – Jan Bashinski DNA Laboratory
Lab 8: PTC Polymerase Chain Reaction Lab
© 2013 Elsevier, Inc. All rights reserved.
PCR genotype analysis to determine RNP-mediated knockout efficiency in C. lusitaniae. PCR genotype analysis to determine RNP-mediated knockout efficiency.
Optimization of a Relative Telomere Length Assay by Monochromatic Multiplex Real- Time Quantitative PCR on the LightCycler 480  Anthony Y.Y. Hsieh, Sara.
mRNA Sequencing Sample Preparation
© 2013 Elsevier, Inc. All rights reserved.
High-throughput sequencing techniques
Suppression of Wild-Type Amplification by Selectivity Enhancing Agents in PCR Assays that Utilize SuperSelective Primers for the Detection of Rare Somatic.
Molecular diagnosis of viral hepatitis
Consequences of T‐DNA insertion on SWP expression in swp mutant.
Molecular Diagnosis of Autosomal Dominant Polycystic Kidney Disease Using Next- Generation Sequencing  Adrian Y. Tan, Alber Michaeel, Genyan Liu, Olivier.
Bioinformatics Lecture By: Ms AQSAD RASHDA
Andrea Gaedigk, Amanda K. Riffel, J. Steven Leeder 
Visual detection of IS6110 of Mycobacterium tuberculosis in sputum samples using a test based on colloidal gold and latex beads  P. Upadhyay, M. Hanif,
Catherine E. Keegan, Anthony A. Killeen 
Supplemental Figure 3 A B C T-DNA 1 2 RGLG1 2329bp 3 T-DNA 1 2 RGLG2
Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing  Imma Hernan, Emma Borràs, Miguel de Sousa Dias,
David L. Evers, Junkun He, Yeon Ho Kim, Jeffrey T. Mason, Timothy J
Standard (Sanger) sequencing
PCR amplification of the ORF encoding the cytosolic p36 protein of M
Genomic DNA Sample Preparation
Genomic structure of LTBP-4 around the 3rd 8-Cys repeat.
Mitochondrial DNA as a Cancer Biomarker
Presentation transcript:

University of Oklahoma Genome Center4/14/12

University of Oklahoma Genome Center4/14/12

The line was extrapolated from 3 data points, 100, 120 and 150 ul of amplification primer University of Oklahoma Genome Center4/14/12

Suggested Optimal Amount of Amplification Primer (ul) for Various Average Sized Template DNAs (bp) 4 Average Template DNA Size (bp) Optimal Amount of Amplification Primer (ul) University of Oklahoma Genome Center4/14/12

Most recent amplicon sequencing results 5University of Oklahoma Genome Center4/14/12 For this amplicon run: – we loaded 1800K beads made from a mixture of amplicons of ~300 and ~500 bases each (see slide 5) on each half of the plate (3600K beads total) using 100 ul of amplification primer on one half and 120 ul of amplification primer on the other half. This run yielded 1,232, 028 reads that passed the filter, with 445,121,246 total bases for an average read length of 362 bases/read. The average read length for each of the 4 sample sets is shown on the next slide.

Average Read length for ~500 and ~300 bp fragments 6 We conclude that both sets of sequence reads cover the full length of the respective amplicons University of Oklahoma Genome Center4/14/12

Read length distribution for 1 kb genomic DNA fragments 7University of Oklahoma Genome Center4/14/12