Www.roche-applied-science.com 1 Content Principles and advantages of melting-curve based genotyping LightCycler ® 480 Genotyping Software - examples Discrimination.

Slides:



Advertisements
Similar presentations
Rob Brown. To think about how we can save money in the lab. To discuss how Haemochromatosis testing has changed and developed over time in Newcastle and.
Advertisements

Getting Started on the Rotor-Gene-6000
DL Windows Software “Rules” Import a CSV File From Excel
Corporate Property Automated Information System (CPAIS) Macro Walkthrough Guide for Excel Version 2003.
Kanban Task Manager for Outlook ‒ Introduction
DNA was extracted from whole blood using 3 extraction instruments: Radius (Protedyne, Windsor, CT) and MagNA Pure (Roche Applied Science, Indianapolis,
Droplet digital PCR Overview and applications
Kanban Task Manager Single‒ Introduction
TOP, The Output Processor TOP, The Output Processor  Training Presentation Electrotek Concepts.
:NEUROPSYCHIATRIC GENETICS [BIOSTATISTICS|BIOINFORMATICS] CORE BIOSTATISTIC/BIOINFORMATIC TOOLS FOR GENETICS DATA: DATA MANAGEMENT AND ANALYSIS RICHARD.
Figure 1. Melting curve of SNP marker D1 of probe and PCR amplicon on LightScanner. SNA D1 is CA or CA deletion. It is very clear to see the genotype by.
Graph these numbers. 1. Highlight the rows you need for your axes 2. Click on the chart wizard icon.
SNP Genotyping Without Probes by High Resolution Melting of Small Amplicons Robert Pryor 1, Michael Liew 2 Robert Palais 3, and Carl Wittwer 1, 2 1 Dept.
The Report Tab. Please select a button to learn more. Welcome to the Report Tab. Here you can view the status of all the projects that you are a part.
High Resolution Melting
Center for Homogeneous DNA Analysis - Software April 21, 2005.
Results Interpretation and Database Management
What Can You Do With qPCR?
Real Time PCR as a Diagnostic Tool. PCR = Polymerase Chain Reaction A way to make lots of copies of DNA What Happens in the Machine? Do the PCR virtual.
X-ray Diffraction Outline Crystals and Bragg Diffraction
Press Esc to Exit ©2011 Cengage Learning. All Rights Reserved. May not be scanned, copied or duplicated, or posted to a publicly accessible website, in.
IN THE NAME OF GOD. PCR Primer Design Lecturer: Dr. Farkhondeh Poursina.
High Resolution Melting: History, Technology, and Utility Charles Hardwick, Ph.D Field Applications Consultant HRM - utilized.
Genetic and Molecular Epidemiology Lecture III: Molecular and Genetic Measures Jan 19, 2009 Joe Wiemels HD 274 (Mission Bay)
The LightScanner ® System Achieve High Throughput Mutation Discovery and Genotyping.
© Copyright 2009 by the American Association for Clinical Chemistry Enrichment and Detection of Rare Alleles by Means of Snapback Primers and Rapid-Cycle.
Real time RT-PCR Quantitating Gene Expression.
Quantification of RNA by real-time PCR
How to use ImageJ to perform mahidol cephalometric analysis
What is it? Infotronics Enterprise Solution SQL based application
Basic Reporting. 2  How to select a Quantification Calculation type.  How to choose a report destination.  How to save a report to a file.  Report.
WORKING WITH MACROS Session Taught by Jennifer Garbett and Zahra Khushbakht.
Real-Time Quantitative PCR Basis
MzGroupAnalyzer tutorial last updated: February 2014.
Processing Workshop. What is processing? “Processing is an open source programming language and environment for people who want to program images, animation,
Microsoft Office Excel By : Juan Pratama Anandika Year : 7 Project Presentation : ICT.
Excel 2007 Non-Mathematical Uses of Excel. DASD Technology Click column
Estimating Crop ET from Satellite Section 1. download satellite data and visualization-V8.
Factor V Leiden Detection and Genotyping
Chem. 133 – 1/26 Lab Lecture. Lab Topic: Data Processing How to Set Up Folders Saving Raw and Processed Data Excel Processing of Raw Data.
Unity Application Generator How Can I… Import control modules (Instrument list) from PID Into the UAG.
THE MOUSE Left Click THE MOUSE Right Click.
Contract Compliance: Reporting
Microsoft Excel Illustrated
EXCEL Create a Pie Graph.
Dreamweaver B 簡至攸.
How to make a visual aid in MS Power Point
Creating a Class Notebook in OneNote
ZXWR RNC Routine Maintenance
Steps to respect : First create a folder where yo will save all the images Draw the first image (basic image) or open it Save your first image in the folder.
Chapter 1 Functions.
Genes and Inheritance Review
Formatting a Worksheet
MBOX Converter Convert MBOX to EML, MSG, RTF & HTML
Excel Spreadsheets 1/28 I can… BW… Work with basic functions in Excel
Formatting a Worksheet
أ.إسراء الطريقي أ. هاله الشملان , 102 تقن , المعمل الخامس
Homogeneous Polymerase Chain Reaction Nucleobase Quenching Assay to Detect the 1-kbp Deletion in CLN3 That Causes Batten Disease  Paul G. Rothberg, Denia.
Webropol – getting started 8
Interferon λ 3 and 4 Genotyping Using High-Resolution Melt Curve Analysis Suitable for Multiple Clinical Sample Types  François M.J. Lamoury, Sofia Bartlett,
Hints on Exporting Data From HQ BOA Into Microsoft Excel
Quick Start Guide   Export data GM Pro 7.4.
Use of Single Nucleotide Polymorphisms (SNP) and Real-Time Polymerase Chain Reaction for Bone Marrow Engraftment Analysis  Dwight H. Oliver, Richard E.
Rapid and Inexpensive Detection of α1-Antitrypsin Deficiency-Related Alleles S and Z by a Real-Time Polymerase Chain Reaction Suitable for a Large-Scale.
Iris Schrijver, Tiffanee J. Lenzi, Carol D. Jones, Marla J
A Simple and Rapid Genotyping Assay for Simultaneous Detection of Two ADRB2 Allelic Variants Using Fluorescence Resonance Energy Transfer Probes and Melting.
Rebecca L. Margraf, Rong Mao, Carl T. Wittwer 
Genotyping of Human Platelet Antigens 1 to 6 and 15 by High-Resolution Amplicon Melting and Conventional Hybridization Probes  Michael Liew, Lesa Nelson,
Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system. Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system.
Instructions for using the Miradi Companion Reporting Tool
Presentation transcript:

1 Content Principles and advantages of melting-curve based genotyping LightCycler ® 480 Genotyping Software - examples Discrimination by allel specific PCR, end-point genotyping on the LightCycler ® 480 System High-Resolution Melting for mutation scanning, genotyping and GC-tail Tm shift

2 Allel Specific PCR Allel 1 Allel 2

3 LightCycler ® 480 End-Point Genotyping Analysis of Hydrolysis Probe Assays Excel macro (“Taqxel” tool) available for analysis of LightCycler ® 480 data

4 Create LightCycler ® 480 Data for “Taqxel Tool” Analysis (1) After PCR with Hydrolysis probes (run on LC480 or another instrument) perform an endpoint measurement by programming a short "Melting Curve" from 60-61°C.

5 After run open analysis "Tm Calling" and export raw data with a right mouse click into the Melting Curves graph, save as.xml format:set filter combination: 533; color comp: on, for FAM data set filter combination: 568; color comp: on, for VIC/Hex data Create LightCycler ® 480 Data for “Taqxel Tool” Analysis (2)

6 On excel: Open FAM.xml and VIC.xml Create LightCycler ® 480 Data for “Taqxel Tool” Analysis (3)

7 Open “Taqxel tool“ and copy/paste the FAM and VIC excel sheets into the respective FAM/VIC folder of the analysis macro “Taqxel Tool” for the Analysis of LightCycler ® 480 Data (4)

8 Click on Graph to visualize groups homozygote FAM homozygote VIC heterozygote “Taqxel Tool” for the Analysis of LightCycler ® 480 Data (5)

9 negative “Taqxel Tool” for the Analysis of LightCycler ® 480 Data (6)

10 unknown “Taqxel Tool” for the Analysis of LightCycler ® 480 Data (7)

11 Click on Analyse to visualize the listed genotypes and to adjust angle settings “Taqxel Tool” for the Analysis of LightCycler ® 480 Data (8)