qPCR NEWS - free REST 2009 version

Editor www.Gene-Quantification.info via methods%40net.bio.net (by editor from gene-quantification.info)
Wed Dec 23 08:03:32 EST 2009


qPCR NEWS - free REST 2009 version




Dear qPCR NEWS Reader,

Best Wishes for the Holiday Season and a Happy and Successful New Year
2010

Our newsletter informs about the latest news in quantitative real-time
PCR (qPCR and qRT-PCR), which are compiled and summarised on the Gene
Quantification homepage. The focus of this newsletter issue is:

- new REST 2009 Version  =3D>  http://www.REST.eu.com
- Call for Abstracts - qPCR 2010 event in Vienna =3D> http://www.qPCR2010-V=
ienna.net
- Download Call =3D> http://www.bioeps.com/qpcr2010/call-for-abstracts-qPCR=
-2010.pdf
- Download course brochure 2010 =3D> http://www.gene-quantification.de/bioe=
ps-course-programm-2010.pdf
- Register here =3D> http://site.bioeps.com/index.php?option=3Dcom_seminar&=
Itemid=3D6

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REST 2009 Software
For gene expression analysis using real-time PCR data from the Rotor-
Gene Q and other cyclers

Estimates up and down regulation for gene expression studies
Analysis using randomization and bootstrapping techniques
Graphical data output via whisker-box plots
REST 2009 Software is a standalone software tool, developed by M.
Pfaffl (Technical University Munich) and QIAGEN, for analysis of gene
expression data from quantitative real-time PCR experiments.

Click the "Resources" tab to download REST 2009 Software free of
charge  =3D>  http://www.REST.eu.com

REST 2009 Software is intended for molecular biology applications.
This software is neither intended for the diagnosis, prevention, or
treatment of a disease, nor has it been validated for such use either
alone or in combination with other products. Therefore, the
performance characteristics of the product for clinical use (i.e.,
diagnostic, prognostic, therapeutic, or blood banking) are unknown.

Principle
REST 2009 Software applies a mathematic model that takes into account
the different PCR efficiencies of the gene of interest and reference
genes. Compared to using a single reference gene, using multiple
reference genes for normalization can improve the reliability of
results.

Traditional relative quantitation enables estimation of gene
expression. However, this method does not provide statistical
information that is suitable for comparing expression in groups of
treated and untreated samples in a robust manner. The integrated
randomization and bootstrapping methods used in REST 2009 Software
test the statistical significance of calculated expression ratios and
can be used even when the data includes outliers. REST 2009 Software
provides additional features for convenient and robust data analysis
(see table "Convenient and robust data analysis").

Convenient and robust data analysis
Feature  Description - REST RG mode An optional input method allows
users to copy and paste results from a Rotor-Gene Q comparative
quantitation analysis rather than importing standard curve and CT
results.
Whisker box plots export  - Expression variation for each gene is
visualized in a whisker-box plot to highlight potential issues, such
as a distribution skew. Whisker-box plots are exported by right-
clicking the graph.
Improved randomization - Randomization algorithms have been improved
for better confidence intervals and more accurate p values.
Handling of standard curve variation - Improvements have been made to
the calculation of confidence intervals and p values. Efficiency is
determined using the best fit for the standard curve and is used in
the randomization process.

REST 2009 Software is suitable for gene expression analysis using real-
time PCR data from the Rotor-Gene Q and other cyclers.


Free Download REST 2009 Software  =3D>  http://www.REST.eu.com

Download User Guide  =3D>  REST 2009 Software User Guide - English
(PDF)  http://www.gene-quantification.de/REST_2009_Software_User_Guide.pdf


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Call for Abstracts - qPCR 2010 event in Vienna
7th =96 9th April 2010 in Vienna
http://www.qPCR2010-Vienna.net

The great international interest of the previous International qPCR
Events from 2004 to 2009 with up to 600 participants from over 40
countries, and 32 international companies in the Exhibition motivates
repeating the success next year in Vienna - qPCR 2010 Vienna
international symposium 7th =96 9th April 2010. The focus of the qPCR
2010 Event will be =93The ongoing evolution of qPCR=94 representing all
new and emerging techniques, applications and data analysis methods:
MIQE Gudelines, HRM, microRNA, CNV, single-cell qPCR, digital PCR, and
analysis of circulating nucleic acids will be in the focus of the
conference. The talks topics by the keynote lecturer and selected
invited academic speakers will be published in a METHODS special qPCR
issue with the title =93The ongoing evolution of qPCR=94, at the meeting
in cooperation with Elsevier.

Why Vienna?  The Vienna region is Austria=92s largest life sciences
location. The Austrian government and the City of Vienna set up a
biotechnology network (LISA VR www.lisavr.at) with the aim of having
one central body to provide support and advice to start-ups and high-
tech companies in the biotec field. Currently 175 life science
companies employ 11,000 people in the greater Vienna region. In
addition an estimated 4,500 academic researchers work in the life
science sector. Vienna is the economic and biotechnology hub for
Central and Eastern Europe and has become an innovative center for the
life science in recent years.

The event is structured in two parts:
1)  an international qPCR Symposium taking place April 7 - 9,
including various talk sessions in the big lecture hall fitting 350
persons,
2)  a parallel qPCR Industrial Exhibition with 32 companies in the
Aula and the Basement of the Juridicum (Juridicum der Universit=E4t
Wien) directly in the city center of Vienna.

We have the pleasure to announce the Call for Abstracts for the qPCR
2010 Event !

Register and submit your abstract now  =3D>   http://submission.qPCR2010-Vi=
enna.net
Deadline to submit an abstract is 31st January 2010.

Symposium sessions:

- MIQE and QM strategies in qPCR
- High throughput quantitative PCR =96 digital PCR
- HRM =96 High Resolution Melting - Epigenetics
- CNA - Circulating nucleic acids
- Single-cell qPCR
- RNAi - microRNA - siRNA Applications =96 miRNA normalisation
- qPCR BioStatistics & BioInformatics

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Symposium sessions & preliminary titles

MIQE and QM strategies in qPCR
The MIQE guidelines: minimum information for publication of
quantitative real-time PCR experiments. Following these guidelines
will encourage better experimental practice, allowing more reliable
and unequivocal interpretation of qPCR results. QM strategies in real-
time PCR to guarantee better and more valid results.
Prof. Stephen Bustin,  =93The MIQE Guidelines:  Minimum Information for
Publication of Quantitative Real-Time PCR Experiments=94
Prof. Christine Mannhalter,  "Standardization efforts of qPCR: Example
BCR-ABL Translocation"
IT-IS Lifescience,  "Optical artefacts: Cause, Consequence,
Correction"

High throughput quantitative PCR =96 digital PCR
384 well applications, new high throughput platforms, droplet PCR,
qPCR robotics, digital PCR, gene expression real-time RT-PCR arrays
(mRNA and microRNA), quantitative multiplexing, =85
Prof. Mikael Kubista,  =93Digital PCR and intracellular expression
profiling=94
Dr. Philip Day,  =93High throughput droplet PCR=94
Dr. Ken Livak,   "High Throughput Gene Expression Profiling of Single
Cells"
Dr. Dr. Simone Kreth,  "Prognostic Impact of Gene Expression Analyses
in Human Glioblastoma"
Dr. Gudrun Tellmann,  "High-Throughput Gene Expression Analysis Using
the LightCycler Platform"

HRM =96 High Resolution Melting - Epigenetics
SNP analysis, HRM =3D high resolution melt applications, Epigenetics,
methylation markers, HRM platform comparison, =85
Prof. Carl Wittwer,  "High Resolution Melting Analysis"
Prof. Claudio Orlando,  =93High Resolution Melting Analysis in Cancer
Diagnosis=94

CNA - Circulating Nucleic Acids
Analysis of circulating RNAs and DNA and microRNAs as diagnostic and
prognostic marker, =85
Dr. Pamela Pinzani,  =93Cell free circulating DNA=94
Dr. Alfred Sch=F6ller,  "Targeting the human urine RNAome for tumor
diagnostics by qPCR=94
Dr. Jim Huggett,  "Diagnostic tools for measuring cell free nucleic
acids. What can we expect from the next decade?=94

Single-cell qPCR
Single-cell sampling, pre-amplification techniques, laser
microdissection, sub-cellular PCR, micro-manipulation of cell
clusters, cellular micro injection, FACS spotting, single cell
handling, pre-amplification=85
Dr. Michael W. Pfaffl,  =93Quantitative expression analysis after pre-
amp in single WBCs=94
Dr. Anders Stahlberg,  =93Single-cell gene expression profiling=94
Dr. Petra Hartmann,  "Analysis of Single Circulating Tumour Cells
isolated from Gastro-Intestinal Cancer Patients"

RNAi - microRNA - siRNA Applications =96 miRNA normalisation
RNAi mechanism, microRNA extraction, qRT-PCR technologies to detect
microRNA, microRNA normalisation strategies, siRNA applications in
combination with qRT-PCR, microRNA targets and microRNA precursors,
new siRNA manipulation and microRNA technologies, ...
Prof. Jo Vandesompele,  =93MicroRNA and mRNA gene expression
normalization=94
Dr. Mirco Castoldi, "Expression profiling of microRNA by quantitative
real time PCR, what is available and where to go from there"

qPCR BioStatistics & BioInformatics
software applications, data mining, calculation of relative
expression, primer and probe design on mRNA and microRNA level, real-
time PCR efficiency determination, mathematical modelling,
multivariate expression profiling, statistics in real-time PCR, data
management, multiway expression profiling, multiple regression
analysis,  3D data visualization, ...
Dr. Ales Tichopad,  =93Statistical aspects of quantitative PCR
experiment design and qPCR data analysis=94
Dr. Jan Hellemans,  =93Accurate and objective copy number profiling
using real-time quantitative PCR=94
Dr. Anders Bergkvist,  =93Expression profiling - clusters of
possibilities=94
Dr. Jan Ruijter,  "Determining PCR efficiency and Cq value after
monitoring PCR amplification with hydolysis probes"


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BioEPS GmbH - qPCR Application Workshops

Life Science is still a growing sector and new methods and
technologies are continously developed. Therefore permanent training
and education becomes so important.

With our specific course program we are offering a range of high-
quality course modules, in cooperation with different companies to
give a general and independent overview of existing qPCR technologies
and systems. Our course issues are based on skilled know-how from own
research studies and publications.

Our aim is to point out a critical way of thinking to increase the
quality and outcome of experimental data.


All courses are held regularly in Freising-Weihenstephan, Germany, in
German and English language.
Further customized workshops and specialized trainings will be held as
well across Europe and world-wide.
Workshops are powered by BioEPS GmbH, located at the campus of the
Technical University of Munich, in Freising-Weihenstephan, very close
to the Munich Airport (MUC).
For more information and registration, please see our web page =3D>
http://workshops.gene-quantification.info/

Course Occasions 2010:

3-day qPCR Basic Module
2-day BioStatistics & Expression Profiling Module
3-day single-cell qPCR
2-day microRNA qPCR
1-day HRM     NEW !
2-das qPCR-R data analysis   NEW !
1-day Project Management     NEW !
2-day Quality Management    NEW !

Download course brochure 2010 =3D> http://www.gene-quantification.de/bioeps=
-course-programm-2010.pdf

Register here =3D> http://site.bioeps.com/index.php?option=3Dcom_seminar&It=
emid=3D6

Access to our workshops =3D> http://www.gene-quantification.de/bioeps-acces=
s.html


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Forward Please send the qPCR NEWS to further scientists and friends
who are interested in qPCR !


Best regards,

Michael W. Pfaffl
responsible Editor of the Gene Quantification Pages
http://www.gene-quantification.info



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