2nd CRISPR Congress Boston, 23-25 February 2016

February 23-25 2016 | Boston, USA
• Improve Target Specificity & Efficiency of Genome Editing
• Enhance Drug Discovery & Screening Applications
• Design & Develop Clinical Therapies
2nd
Annual
Rachel Haurwitz
Caribou Biosciences
Jon Moore
Horizon Discovery
Alexandra Glucksmann
Editas Medicine
Emmanuelle Charpentier
Max Planck Institution, Umeå University
George Church
Harvard Medical School
Rodger Novak
CRISPR Therapeutics
This is
designed to
describe the
profound
impact CRISPR
is having
on basic
research and
therapeutic
development. It
will explore the
research tools,
bioinformatics
and expertise
needed to
make the
most of this
breakthrough
technology.
Eric Rhodes, Horizon
Lead Partner Additional Event Partners
Tel: +1 212 537 5898 | Email: info@hansonwade.com
RESEARCHED & DEVELOPED BY:crispr-congress.com

Welcome to Those Dedicated to CRISPR
2.Engineer the next generation of humanized
animal models cell lines for improved
disease modeling and preclinical predictability
2. Harness CRISPR technology for more
accurate gene editing in non-eukaryotic
bacterial and plant cells
5 Key Benefits to Takeaway
1. Discover innovative ways to measure and
optimize specificity of the CRISPR/Cas9
system in order to reduce off target effects
1. Effectively adopt the lentiviral delivery system
to optimize genome wide targeting from basic
research to drug discovery
3. Develop strategies to perform large scale
genome wide screening from basic research
to disease target identification
3.Utilize CRISPR/Cas9 to develop robust cell-
based cancer immunotherapies including
CAR-Ts and TCRs
4. Learn how to independently design and
optimize CRISPR with novel emerging
enzymes (Cpf1) to enhance the precise
nature of genome editing
4. Understand the regulatory requirements
for CRISPR/Cas9 mediated therapeutic
development as it is poised to demonstrate
clinical utility
5.Enhance the delivery and efficiency of
CRISPR/Cas9 in primary cells
5.Harness CRISPRi to elevate the regulation of gene
expression through epigenetic modifications
5 Key Ideas to Implement
Tel: +1 212 537 5898 Email: info@hansonwade.com
crispr-congress.com #CRISPR2016 CRISPR Precision Genome Editing
2nd
Annual CRISPR Precision Gene Editing Congress
Boston, USA | February 23-25 2016
Achieve the Full Potential of CRISPR Genome Editing to
Ensure Accuracy Success
Optimize your CRISPR Design to Efficiently Power Novel Applications in Drug
Discovery, Screening and Therapeutic Development
The 2nd Annual CRISPR Congress will enhance the basic
research, drug discovery and therapeutic applications
of CRISPR technology by overcoming key specificity,
efficiency and delivery challenges needed to improve the
precise editing and repair of the genome.
With the superior applications of CRISPR showing no signs
of relenting, join the leading CRISPR figureheads as they
reveal advanced methodology, strategies and clinical
timelines that maximize the power of precision genome
editing and fulfill its revolutionary potential.
As well as applying CRISPR to optimize the custom
development of stable cell lines disease models for
target identification and enhanced drug discovery, CRISPR
Congress 2016 pioneers the translation of CRISPR-based
gene therapies into a clinically relevant transformative
therapy.
As CRISPR continues to create a sea change for genetic
research, not to mention the next class of enzymes on
the horizon, join the CRISPR Congress to deepen your
understanding, minimize off-target effects and elevate
delivery mechanisms for therapeutic use. There is a
a key opportunity for you to network and build future
collaborations with fellow peers to optimize the application
of CRISPR gene editing technology and transform
your research to the next level.
Why the 2nd CRISPR Congress Should Be in Your Calendar

Speaker Faculty
2nd
Rachel Haurwitz
President CEO
Caribou Biosciences
Alexandra Glucksmann
Chief Operating Officer
Editas Medicine
Emmanuelle Charpentier
Director
Max Planck Institution for
Infection Biology, MIMS
Umeå University
George Church
Professor of Genetics
Jon Moore
CSO
Horizon Discovery
John Feder
Associate Director of
Genome Biology
Bristol-Myers Squibb
TJ Cradick
Head of Genome Editing
CRISPR Therapeutics
Joel Klappenbach
Director of Applied
Genomics
Merck
Gregory Davis
RD Manager, Molecular
Biotechnology
Sigma-Aldrich
Charles Gersbach
Associate Professor, Director,
Center of Biomolecular
Tissue Engineering
Duke University
David Root
Senior Director, Broad
Institute Genetic Perturbation
Platform and the Functional
Genomics Consortium
Channabasavaiah
Gurumurthy
Assistant Professor-
Genetics, Director- Mouse
Genome Engineering Core
Facility, University of
Nebraska Medical Center
Greg Gocal
Senior Vice President RD
Cibus
Benjamin Kleinstiver
Postdoctoral Fellow,
Keith Joung’s Group,
Massachusetts General
Hospital Harvard Medical
School
Lorenz Mayr
VP Global Head, Reagents
Assay Development
AstraZeneca
John Doench
Associate Director,
Genetic Perturbation
Platform, MIT
Harvard University
Jennifer Berman
Staff Scientist,
Applications, Digital
Biology Center
Bio-Rad Laboratories
Rodger Novak
Chief Executive Officer
CRISPR Therapeutics
Jonathan Gootenberg
Feng Zhang’s Lab, Broad
Institute, MIT
Harvard University
Jason Potter
Senior Scientist Manager
Thermo Fisher Scientific
Shawn Zhou
Senior Scientist
Genscript
Wen Xue
Assistant Professor, RNA
Therapeutics Institute,
University of Massachusetts
Anja Smith
Director of RD
Dharmacon,
GE Healthcare
Mark Behlke,
Chief Scientific Officer
Integrated DNA
Technologies, Inc
Daniel Anderson
Sam Goldblith Associate
Professor
Massachusetts Institute of
Technology (MIT)
Join the Discussion on
SEARCH GROUPS FOR:
CRISPR Precision Genome Editing
to join the online community.

Conference Day One
8.00 Registration, Breakfast Networking
9.00 Chair’s Opening Remarks
CRISPR the Superior: A Revolution That Speeds On
9.10 Keynote Interviews: Optimizing CRISPR Design to
Efficiently Power Novel Applications in Drug Discovery,
Screening and Therapeutic Development
The panel will discuss and answer the following questions:
• How has the novel CRISPR enzyme Cpf1 enhanced the application
CRISPR technology?
• With continued innovation - will CRISPR always be at the top or are
there better alternatives emerging to drive gene engineering?
• How has the industry tried to enhance CRISPR/Cas9 mediated gene-
editing in primary cells?
• How is the industry addressing the ethical challenges surrounding
genetic editing of germline cells in order to be diligent whilst
pushing scientific boundaries?
• From a therapeutic perspective, how close are we to demonstrating
clinical utility and what have been the lessons learning in preparing
CRISPR-based gene therapies for human trials?
Emmanuelle Charpentier, Director, Max Planck
Institution for Infection Biology, MIMS,
Umeå University
Alexandra Glucksmann, Chief Operating Officer,
Editas Medicine
Rodger Novak, Chief Executive Officer,
CRISPR Therapeutics
Rachel Haurwitz, President CEO,
Caribou Biosciences
10.00 Using CRISPR as a Screening Tool for Genomic Target
Validation Screens and to Identify Novel Drug Targets
• Learn to accurately analyze data from screens and to functionally
validate them
• Genome wide screening for gain of function or loss of function
screening, either in exploring the developmental state for basic
biology or for screening for therapeutic targets for diseases
(drug development)
• Discover how to establish CRISPR libraries for target identification
Jon Moore, CSO, Horizon Discovery
10.30 Morning Refreshments Speed Networking
Measuring and Optimizing Specificity of the CRISPR/Cas9 System
11.30 Keynote Presentation: The CRISPR-Cas9 Revolution in
Genome Engineering: Lessons Learned from Bacteria
• Addressing the origins of CRISPR-Cas9
• Discover the mechanisms of CRISPR-Cas9 and to highlight the
evolution of CRISPR-Cas9
Emmanuelle Charpentier, Director, Max Planck
Institution for Infection Biology, MIMS, Umeå
University
12.15 Beyond Cas9: Discovering New Tools for Precision
Genome Editing
• Using smaller, easier to deliver Cas9 orthologs enables new
translational applications for genome editing
• Cas9 is just one of many programmable nucleases in nature with
gene editing potential
• The RNA-guided endonuclease Cpf1 expands the genome
engineering toolbox and allows for allele-specific targeting
Jonathan Gootenberg, Feng Zhang’s Lab,
Harvard University
12.45 Ultra-Sensitive Quantification of Genome Editing Events
by Droplet Digital PCR
• Genome editing events can be rare and difficult to quantify, with
frequencies 5% in some targeted cell types
• Genome editing methods development and optimization would
benefit from a sensitive, rapid-readout tool for edit validation and
off-target detection
• Droplet Digital PCR (ddPCR) enables sensitive (0.1%), precise
absolute quantification of NHEJ and HDR alleles in a rapid, high-
throughput format
Jennifer Berman, Staff Scientist, Applications,
Digital Biology Center, Bio-Rad Laboratories
2nd
Tuesday February 23rd 2016

16.45 Breakout Roundtables: Advancing CRISPR Technology to The Next Level
Discover multiple perspectives on the key issues and applications in the revolutionary CRISPR field by joining roundtable
discussions, specifically designed so you can learn from your fellow gene-editing peers.
Moderators:
Joel Klappenbach, Director of Applied Genomics, Merck
Jon Moore, CSO, Horizon Discovery
Daniel Anderson, Sam Goldblith Associate Professor, Massachusetts Institute of Technology (MIT)
Discovering how to
perform high throughout
genome screenings
in the development of
CRISPR libraries
5.
Collaborating to
develop and define
protocols for gene
editing in non-
eukaryotic cells
4.
Advancing non-viral delivery
methods to progress
CRISPR-therapeutics – how
can you refine methodology
to overcome this key hurdle
of CRISPR therapeutic
development in the context
of clinical utility
3.Harnessing CRISPRi
technology to fast-track
development of therapies
– ensuring sequence
specific control of
gene expression
2.Evaluating and combining
different methods to
enhance specificity
of CRISPR to minimize
unwanted
off-target effects
1.
13.15 Networking Lunch
14.15 From “Gene Editing” to True Genome-Scale Engineering
• Reducing issues with competing events like Non-Homologous
End-Joining (NHEJ) and efficiency of large construct insertion/
replacements in homologous recombination editing
• Overcoming NHEJ events with the use of a promising alternative
to double-strand breaks (CRISPR, dual nickase or FokI) via
recombinase/integrase mechanisms
George Church, Professor of Genetics,
14.45 Genome Editing Solutions - New Workflow Tools for
Genome Editing
• High Efficiency editing in difficult cell lines using cas9 mRNA or RNPS
• Improved delivery using Neon electroporation or Lipofectamine
CRISPRMAX
Jason Potter, Senior Scientist Manager,
15.15 How Epigenome Editing Can Be Used to Reprogram
Cell Phenotype for Disease Modeling and Regenerative
Medicine
• Insight into how epigenome editing tools have been developed to
perturb gene regulatory elements
• Annotating the function of regulatory elements can be used
to discover new drug targets, diagnostics, and strategies for
personalized medicine
Charles Gersbach,
Associate Professor, Director, Center of
Biomolecular Tissue Engineering,
Duke University
15.45 Afternoon Refreshments Poster Session
16.15 Beyond the Break: Options for Donor-DNA Driven
Genome Editing with High Fidelity and Efficiency
• Donor DNA formats and their impact on DNA repair rates
• Learn to manipulate DNA repair outcomes among diverse cell types
• Strategies for pooled screens using CRISPR and donor-DNA libraries
Gregory Davis, RD Manager, Molecular
Biotechnology, Sigma-Aldrich
17.45 Chair’s Closing Remarks Jon Moore, CSO, Horizon Discovery
17.50 Evening Drinks Reception Hosted by Horizon Discovery
2nd

2nd
Conference Day Two
8.00 Breakfast Networking
9.00 Chair’s Opening Remarks
Advancing Large Scale Genome Wide Screening
9.10 Harnessing the Power of CRISPR to Improve Drug
Discovery Across Key Therapeutic Areas
• Optimizing experimental design and data analysis to validate hits
from the screens
• Evaluating the genes to knock-out to eliminate expression of target
gene and subsequent genes to build the have workout interactions
Lorenz Mayr, VP Global Head, Reagents
Assay Development, AstraZeneca
9.40 Innovative Trait Development Tools in Plant Breeding will be
Crucial for Doubling Global Agricultural Productivity by 2050
• Rapid Trait Development System (RTDS™) employs Gene Repair
OligoNucleobases (GRONs) to make defined spelling changes in
genomic DNA
• We report that RTDS can significantly improve the outcome of
double strand break activity by reliably inducing precise and targeted
nucleotide spelling changes closely aligned to the cut site
• Our work demonstrates the significance of gene editing to rapidly,
precisely and reliably improve cro performance to develop any trait
in commercially relevant crop varieties
Greg Gocal, Senior Vice President, Research
Development, Cibus
10.10 Opportunities and Challenges of Applied Genome
Engineering Technologies in the Pharmaceutical
Research Setting
• Genome engineering is advancing at an incredible pace however,
applications across the types of translational and predicative cell
models now preferred for drug target discovery remains a challenge
• What areas of the drug discovery process will genome engineering
have the biggest and most immediate impact
• How does the pharmaceutical industry evaluate and implement a
technology that is evolving so rapidly
John Feder, Associate Director of Genome
Biology, Bristol-Myers Squibb
10.40 Improving CRISPR-Cas9 Gene Knockout with a Validated
Guide RNA Algorithm
• Development of an algorithm for improved CRISPR RNA functionality
and specificity
• Utility of a synthetic two-RNA approach for high-throughput arrayed
gene knockout
• Importance of rigorous alignment tools for CRISPR RNA specificity
Anja Smith, Director of RD,
Dharmacon, GE Healthcare
11.10 Morning Refreshments
11.40 Understanding the Regulatory Requirements for CRISPR/
Cas9 Mediated Therapeutic Development
• Addressing the safety aspects involving specificity and understanding the
proper usage and safety concerns of different delivery techniques
• Learnings from other gene editing tools in the clinic
• WhatistheregulatorypathwayandhowequippedornotareEFSAandtheFDA
• Addressing successful case studies involved in regulatory path of
TALENs or ZFNs
Alexandra Glucksmann, COO, Editas Medicine
Wednesday February 24th 2016

Harnessing CRISPR Technology in Disease and Preclinical Modeling
12.10 Optimizing Bioinformatic Tools to Improve Guide Design
and to Enhance Specificity
• Optimize CRISPR/Cas systems to drive gene editing
• Utilize CRISPR corrects the underlying disease-causing mutations
• Harness bioinformatics and design strategies to improve and ensure
specificity
• Discovering the use of new CRISPR systems
TJ Cradick, Head of Genome Editing,
CRISPR Therapeutics
12.40 Tipping the CRISPR NHEJ/HDR Imbalance: Strategies for
Efficient Generation of Large-Size-DNA Knock-in Animal
Models
• Latest developments in enhancing insertion of larger DNA
molecules using HDR-dependent and HDR-independent
mechanisms
• The CRISPR strategies that help rapid development of humanized
animal models
Channabasavaiah Gurumurthy,
Assistant Professor-Genetics, Director- Mouse
Genome Engineering Core Facility,
University of Nebraska Medical Center
13.10 Applying GenCRISPR Efficiently – Pioneering to Make
Genome-Editing Easy
• GenCRISPR services cover mammalian and bacterial cell
line services
• GenCRISPR-related reagents and making research easy through
one-stop service solution
Shawn Zhou, Senior Scientist, GenScript
13.20 Networking Lunch
14.20 Precision Cancer Mouse Models Through Genome Editing
with CRISPR-Cas9
• Address how CRISPR can speed up the generation of precision
cancer models
• How these models can be used to understand the evolution and
progression of individual tumors
• Identify new strategies for cancer treatment
Wen Xue, Assistant Professor, RNA
Therapeutics Institute, University of
Massachusetts Medical School
Maximizing Precision for Novel Applications
14.50 Increase Efficiency of Genome Editing Using the Alt-R™
CRISPR-Cas9 System
• Improving on-target CRISPR-Cas9 genome editing performance
while also reducing cell toxicity and eliminating innate cellular
immune response as compared to in vitro transcribed guide
RNA alternatives
• A discussion on challenges and potential pitfalls of genome editing
with guidance towards successful CRISPR-Cas9 editing experiments
Mark Behlke, Chief Scientific Officer,
Integrated DNA Technologies, Inc
2nd

Is Cpf1 the
start of the
next generation
class of CRISPR
enzymes?
What are the
next exciting
applications on
the horizon?
What are the
fundamental next
steps required to
develop and optimize
CRISPR technology
further?
15.10 Application of CRISPR Technologies to Genetic Screens
• As a powerful tool for large scale screens how do CRISPR libraries
perform in actual screens?
• What factors are experimentally shown to be important?
• What are strengths and limitations of CRISPR libraries and screens?
David Root, Senior Director, Broad Institute
Genetic Perturbation Platform and the
Functional Genomics Consortium
15.40 Afternoon Refreshments
16.10 Genetic Screens with CRISPR-Cas9: Optimizing On-Target
Activity and Avoiding Off-Target Effects
• Considerations for library design to optimize on-target activity
• Detection and avoidance of potential off-target activity
• Comparison of CRISPR to RNAi
John Doench, Associate Director, Genetic
Perturbation Platform, MIT, Harvard University
16.40 Expanding and Improving the Genome-Wide Specificities of
CRISPR-Cas9 Nucleases
• The targeting range of Cas9 can be expanded by engineering
variants that can target previously inaccessible sitesDetection and
avoidance of potential off-target activity
• The genome-wide specificity of Cas9 can be improved with novel
evolved variants
• GUIDE-seq can be used to define the genome-wide specificities of
Cas9 variants
Benjamin Kleinstiver, Postdoctoral Fellow,
Keith Joung’s Group, Massachusetts General
Hospital Harvard Medical School
17.10 CRISPR Roundtable Intelligence Mastermind Discussion
Missed a roundtable you wished you were at or have unanswered questions to your specific challenges? Roundtable
moderators summarize the industry intelligence from the Day 1 Breakout Roundtables, providing you one final opportunity
to outline key future trends for the CRISPR gene editing field. The panel will discuss the following:
17.25 Chair’s Closing Remarks
17.30 Evening Drinks Reception Hosted by Sigma-Aldrich
2nd

Workshop A
2nd
CRISPR technology has rapidly changed the face of biological research. In particular, precision genome editing has been so
readily adopted it has now become routine for many labs. One key application of CRISPR is in the discovery and functional
understanding of genomics through high-throughput screening. In this interactive workshop, attendees will capitalize lessons
learned in order to:
• Develop protocols to carry out large scale genome screens to better understand gene interactions in disease
• Learn from a range of applications to optimize the development of CRISPR libraries
• Optimize data analysis of genome screens for target identification in drug discovery
CRISPR/Cas9-mediated genome editing has become the preferred tool of choice when it
comes to efficiently and easily manipulating the genome with strong specificity. As such,
a rapidly adopted application has emerged to create more physiologically relevant and
predictable in vivo disease models to better understand the complexity of human disease. In
this interactive workshop, attendees will discover solutions and answers to help them:
• Outline the latest in developments in the CRISPR-mediated generation of disease models
• Overcome the current limitations of using CRISPR for disease modeling
• Harness CRISPR gene editing technology to develop humanized animal models,
particularly for emerging immunotherapies
• Address and discuss case studies to standardize protocols to utilize CRISPR for
in vivo models
Performing High Throughout Genome Screenings for Developing CRISPR Libraries
Date: Thursday February 25th 2016 | Time: 9.00am – 12.00pm
Developing More Predictable Disease Models With CRISPR: From
Basic Research to Target Identification and Drug Discovery
Date: Thursday February 25th 2016 | Time: 1.00pm – 4.00pm
TJ Cradick, PhD has studied the different families of nucleases that enable genome editing and gene
therapy, such as for correcting mutations that cause diseases. Recent work has focused on CRISPR/Cas
nucleases (see publication list). Previously we developed and studied TAL Effector Nucleases (TALENs),
and Zinc Finger Nucleases (ZFNs). Many of these studies in academia or industry included measuring
and improving specificity. TJ co-authored manuscripts detailing our bioinformatics web tools: ZFN-Site,
PROGNOS, SAPTA and COSMID (CRISPR off-target).
Workshop Leader
TJ Cradick, Head of Genome Editing, CRISPR Therapeutics
CB Gurumurthy obtained a faculty position at the University of Nebraska Medical Center (UNMC), Omaha in 2007.
He is currently an assistant professor in Developmental Neuroscience Department and serves as the Director of
UNMC Mouse Genome Engineering Core Facility. He is actively pursuing research in developing newer geneome
editing technologies in addition to developing widely-usable animal models for basic and drug discovery research.
Workshop Leader
Channabasavaiah Gurumurthy, Assistant Professor-Genetics, Director- Mouse
Genome Engineering Core Facility, University of Nebraska Medical Center
Workshop B

CRISPR Partners
Sigma-Aldrich
Sigma-Aldrich is proud to offer its newest line of genome editing tools, Sigma CRISPRs, to the global research
community. Sigma CRISPRs offer rapid, reliable and reproducible results – everything you need for gene editing
experiments. Sigma-Aldrich also offers the CRISPR Core Partnership Program providing scientists and core
facilities with world class service and a diverse portfolio of innovative CRISPR reagents, with the support of an
industry-leading bioinformatics engine. The Cell Design Studio team at Sigma Aldrich, utilizes CRISPR, ZFN,
and shRNA technologies to rapidly and efficiently generate model cell lines to be used in basic research, cell-
based assays, target validation and much more.
www.sigmaaldrich.com
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, our mission is to enable
our customers to make the world healthier, cleaner and safer. We help our customers accelerate life
Sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory
productivity. Through our four premier brands Thermo Scientific, Life Technologies, Fisher Scientific and Unity
Lab Services we offer an unmatched combination of innovative technologies, purchasing convenience and
comprehensive support.
www.thermoscientific.com
Program Partner
Program Partner
Bio-Rad
Bio-Rad Laboratories, Inc. designs, manufactures, and distributes a broad range of innovative tools and
services to the life science research and clinical diagnostics markets. Founded in 1952, Bio-Rad has a
global team of more than 7,750 employees and serves more than 100,000 research and industry customers
worldwide through the company’s global network of operations. Throughout its existence, Bio-Rad has built
strong customer relationships that advance scientific research and development efforts and support the
introduction of new technology used in the growing fields of genomics, proteomics, drug discovery, food safety,
and medical diagnostics.
www.bio-rad.com
Program Partner
2nd
Horizon Discovery
Horizon Discovery combines long scientific heritage in translational research with GENESIS™, a
precision gene editing platform incorporating rAAV, CRISPR and ZFN technologies. Horizon supplies
genetically-defined cell lines, gene-editing tools and services, custom cell line generation, molecular
reference standards, and contract research services to approaching 1,000 academic, clinical and
biopharmaceutical organisations.
www.horizondiscovery.com
Lead Partner

CRISPR Partners
Dharmacon – part of GE Healthcare
Dharmacon has revolutionized the field of RNA synthesis with the introduction of 2’-ACE synthesis chemistry
since 1995. As leaders in custom RNA synthesis, Dharmacon was an early participant in the newly discovered
field of RNA interference, and contributed several key scientific findings. Dharmacon RNAi products were some
of the first commercially available. This leadership has continued through technical advances in bioinformatics,
and chemical modifications to improve performance. Today, our areas of research and research tools have
expanded to support all aspects of RNAi interference; siRNA, lentiviral shRNA, tools for microRNA research,
and whole-genome scale libraries for RNAi functional screens of genes, microRNAs and long non-coding RNAs.
Dharmacon also has the largest collection of cDNAs and ORFs commercially available.
In addition, Dharmacon offers a unique set of CRISPR-Cas9 gene editing tools. The Dharmacon CRISPR-Cas9
platform greatly simplifies the workflow of permanently knocking out genes. Our approach includes pre-
designed, ready-to-use DNA and RNA components and enables fast assessment of multiple target sites per
gene for multiple genes. We offer CRISPR Guide RNA, high quality, ready-to-use lentiviral and synthetic reagents
to guide Cas9 cleavage; Cas9 Nuclease for your cell type to ensure robust Cas9 expression or explore DNA-free
options; CRISPR Controls and Detection Primers essential to assessment of CRISPR-Cas9 genomic editing
experiments; CRISPR-Cas9 Pooled sgRNA or arrayed crRNA for high-throughput gene editing studies.
www.dharmacon.gelifesciences.com
Program Partner
Cibus
Cibus has developed plant and microbial platforms enabling it to become a world leader in precision gene
editing, generally, and advanced non-transgenic breeding, specifically. The Rapid Trait Development System
(RTDS™), its proprietary technology for non-transgenic breeding, enables site-specific edits of native genes with
no introduction of foreign DNA. The precise and predictable outcomes can replicate products developed using
traditional mutagenesis and are identical to those that could occur in nature, given enough time. Consequently,
these plants are not considered transgenic, the key attributes of GMO crops.
www.cibus.com
Program Partner
Integrated DNA Technologies
Integrated DNA Technologies (IDT) is a leader in the manufacture and development of products for the
research and diagnostic life science market. The largest supplier of custom nucleic acids in the world, IDT
serves academic research, biotechnology, and pharmaceutical development.
IDT products support a wide variety of applications, including next generation sequencing (NGS), genome
editing, DNA amplification, SNP detection, microarray analysis, expression profiling, gene quantification, and
synthetic biology. Platform-independent NGS products and services are available in addition to DNA and RNA
oligonucleotides, qPCR assays, siRNA duplexes, reagents for CRISPR-Cas9 genome editing, and custom gene
synthesis services.
IDT has an active research and development division that supports product development, and participates in
corporate and academic collaborations. IDT also supports the education of the next generation of scientists
through our regular sponsorship of the international Genetically Engineered Machine (iGEM) competition, and
other scientific outreach activities.
www.idtdna.com
Program Partner
2nd

Contact
Diane McKenna
Portfolio Director, Genomics
Tel: +44 (0)203 141 8700
Email: sponsor@hansonwade.com
Join The CRISPR Partnership:
Advanced Analytical Technologies
Advanced Analytical Technologies, Inc. (AATI), founded in 1998 and located in Ankeny, Iowa, is a world leader in
multi-channel (parallel) capillary electrophoresis. The company’s products are designed to improve processes
within the life science, agricultural, molecular diagnostics, biofuels, biotechnology, and pharmaceutical
industries. Its award winning instrument, the Fragment Analyzer™ is the premier instrument to automate the
analysis of nucleic acid fragments and smears. Designed to improve laboratory workflow and decrease time
to results, the Fragment Analyzer can dependably and reliably assess gene editing events generated through
CRISPR/Cas9 mutagenesis using a streamlined heteroduplexing and cleavage process for ultra-sensitive
detection of fragments and digital data outputs with specially designed software to aid in analysis. Additionally,
Reagent Kits are available to accurately qualify and quantify nucleic acid raw materials like genomic DNA and
RNA and analyze NGS library preparation. The Fragment Analyzer is the premier instrument to automate
analysis of nucleic acids.
www.aati-us.com
Exhibitor
GenScript
GenScript is the leading gene, peptide, protein and antibody research partner for fundamental life science
research, translational biomedical research, and early stage pharmaceutical development. Since our
establishment in 2002, GenScript has exponentially grown to become a global leading Contract Research
Organization that provides services and products to scientists in 86 countries worldwide
www.genscript.com
Spotlight Partner
CRISPR Partners
2nd
The CRISPR Congress was highly successful...a very engaging meeting
Bio-Rad on CRISPR Congress 2015

Code:5792
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1 Workshop
$2698
(save $700)
$2898
(save $500)
$3098
(save $300)
$3198
(save $200)
Bronze Package:
Conference Only
$2099
(save $600)
$2299
(save $400)
$2499
(save $200)
$2699
Workshop Each: $699
2nd
• 10% discount – 3 delegates
• 15% discount – 4 delegates
• 20% discount – 5 or more delegates
Please note that discounts are only valid when three or more
delegates from one company book and pay at the same time.
Team Discounts*
crispr-congress.com/register
Tel: +1 212 537 5898
Email: register@hansonwade.com
Mail: Hanson Wade
4th Floor, 52 Grosvenor Gardens,
London, SW1W 0AU

2nd CRISPR Congress Boston, 23-25 February 2016

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2nd CRISPR Congress Boston, 23-25 February 2016