I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
We are glad to announce the 16th PHENOMIN call for proposals for innovative mouse and rat model generation. PHENOMIN supports scientists to create new models:
Conditions for eligibility: PHENOMIN is committed to reduce the use of animals (3R’s), only nomination of mutant lines that are not available in known repository, are eligible.
Application deadline: January 31st
Scientific evaluation: All the projects will be reviewed by an external panel of experts beyond the technical feasibility and will be ranked and prioritized. A short description of the project and scientific goal (1 page) will be required for the submission.
For all models that will be selected, please consider that:
Since 2011, PHENOMIN has generated close to 300 models for the International Mouse Phenotyping Consortium (knock-out and point mutation mice to decipher the coding genome) and more than 1400 models for the French and International scientific community.
It was a aditionnal INFRAFRONTIER´s new free-of-charge transnational access (TA) call " COVID-19 Therapeutics Pipeline ". The goal was to provide extensive user support to the selected projects for assessing novel potential vaccine and treatment candidates for COVID-19. The TA service is covered by the INFRAFRONTIER2020 project (Horizon 2020).
INFRAFRONTIER partners (PHENOMIN-CIPHE and CCP) execute this call by providing viral particles, COVID-19 mouse models, cohort production, and BSL3 pipeline analysis. Further functional analysis and advanced readouts like organ histopathological analysis, multiplex assay profiling of cytokines and chemokines in lung and mouse serum, etc. can be provided on a collaborative basis outside the TA call scope.
The expert teams are happy about the high value of the submitted projects. Ana Zarubica, PHENOMIN-CIPHE Deputy Director and the PI supervising the COVID-19 Therapeutics Pipeline, says: "The relevance and quality of all proposals was excellent. They are all addressing fundamental clinical issues."
We are glad to announce the 14th PHENOMIN call for proposals for innovative mouse and rat model generation and/or phenotyping. PHENOMIN is able to support scientists to create and phenotype new models to study:
Since 2011, PHENOMIN has generated 265 models for the International Mouse Phenotyping Consortium (knock-out mice to decipher the coding genome) and more than 900 models for the French and International scientific community.
Conditions for eligibility: PHENOMIN is committed to reduce the use of animals (3R’s), only nomination of mutant lines that are not available in known repository, are eligible
Scientific evaluation: All the projects will be reviewed by an external panel of experts beyond the technical feasibility and will be ranked and prioritized
For all models that will be selected, please consider that:
The 14th PHENOMIN call for projects was a great success. Fifty projects were submitted by 30 French researchers from laboratories across the country. 27 projects were selected and supported by the PHENOMIN-CIPHE or PHENOMIN-ICS centers. Most of these projects have already started and will certainly contribute to the influence of French research in various fields.
Applications at the 1st of every month !
Specialized phenotyping in inflammatory condition and functional immune phenotyping screen
The INFRAFRONTIER mouse clinics offer the examination of mouse mutants using a broad and standardised phenotypic check-up covering key research areas such as behaviour, clinical chemistry, immunology, energy metabolism, and lung function amongst others. If phenotypes are uncovered by the primary assays, mouse mutants can be subjected to more detailed analyses in hypothesis driven and disease focussed phenotyping pipelines.
In this specialised phenotyping call we provide access to a comprehensive panel of phenotyping tests, relying on standardized and customized protocols in key therapeutic areas.
1-Induced secondary phenotyping screen under acute or more chronic inflammatory conditions
2-Functional immune-phenotyping screen by mass cytometry is proposed by PHENOMIN-CIPHE, and is dedicated to secondary functional immune-phenotyping screen by mass cytometry toassess the effector functions of immune cells:
More information about these calls
in progress
The project had to be based on scientifically validated preliminary data and the choice of the experimental model must be clearly justified. The call was dedicated only to generating new experimental models for rare diseases i) animal models, ii) in vitro models based on induced pluripotent stem cell (iPSC) (including conditions for archiving lines). Any other request (breeding, phenotyping, advanced imaging etc.) was not eligible.
Animal models
To develop the new experimental animal models of rare diseases, successful applicants will have a facilitated access to experimented platforms for which most of them are being part of CELPHEDIA, the French infrastructure that promotes innovative services and tool on model organisms:
Non-mammalian models
Mammalian models: Rabbit, Rat, Mouse
The precise type of model development (knock-out, knock-in, humanized model, transgenic…), will be specific to each organism, but will rely on the latest improvements and most appropriate techniques of genome editing (ZFNs, TALEN, CRISPR/CAS9, etc.) or more classical transgenic approaches (such as DNA microinjection or lentiviral infection).
Human induced pluripotent stem cell (iPSC) lines
For the development of in vitro models based on induced pluripotent stem cell (iPSC) lines, the best suited approach will be designed for each project. Please pay attention that only projects for which agreements of lineage derivation from iPS of patients have already been obtained will be considered. Human induced pluripotent stem cell (iPSC) lines will be developed with the support of the Platform iPSC Nantes.
The Sientific commitee has selected 8 projects amongst 16 submitted to develope new experimental animal models for rare diseases. New nominated genes for 5 new mouse models and 3 rat models were selected.See the awarded project
More information regarding this pasted call at aap-bio@fondation-maladiesrares.com
Precision mammalian model development / rat models - January 2019
This Trans-national Access call of the INFRAFRONTIER2020 project supports a total of 3 precision rat model development projects. A complementary call provides support for 12 customised mouse model development projects.
The EC Horizon 2020 funded INFRAFRONTIER2020 project (2017 – 2020) supports eligible customers by providing a total of 5 access units in this call.The access unit offered covers the derivation of germ-free (axenic) mice from a breeding nucleus or from frozen materials provided by the applicants. Mice will be kept under germ-free conditions for 6-8 weeks.
More information about this call
1 new rat model have been selected to be carried out by PHENOMIN-ICS for its generation.
Derivation of germ-free mice (axenic service)
This call offers a service to derive germ-free mice for European researchers who study the role of the microbiome in metabolism, physiology, and immune function.The `axenic´ service is free of charge. Access to the axenic service will be granted on the basis of scientific excellence and supports pilot projects for the derivation of-germ-free mice. Further breeding and characterisation of axenic mice or the development of gnotobiotic models can be offered on a fee-for-service or on a collaborative basis.
The EC Horizon 2020 funded INFRAFRONTIER2020 project (2017 – 2020) supports eligible customers by providing a total of 5 access units in this call.The access unit offered covers the derivation of germ-free (axenic) mice from a breeding nucleus or from frozen materials provided by the applicants. Mice will be kept under germ-free conditions for 6-8 weeks.
More information about this call
Specialised Phenotyping - metabolic and behavioral phenotyping pipelines
Main objective of this INFRAFRONTIER2020 Trans-national Access call is to facilitate access for the wider biomedical research community to the unique infrastructure and scientific expertise of the participating INFRAFRONTIER mouse clinics, where mouse mutant lines can be tested through specialised metabolic- and behavioural phenotyping pipelines. Disturbed energy balance regulation results in obesity and in numerous related metabolic disorders such as type 2 diabetes mellitus. We offer specialised phenotyping pipelines comprising state-of-the-art test assays monitoring disease related parameters. In-depth behavioural phenotyping supports the elucidation of the molecular and genetic basis of behavioural impairments that are relevant for human neuropsychiatric disorders such as anxiety disorders, post-traumatic stress disorder, depression, schizophrenia, autism, attention-deficit hyperactivity disorder, Parkinson’s and Alzheimer’s Disease.
Access will be granted on the basis of scientific excellence and supports the development and in depth characterisation of mouse models for investigating gene function and human pathophysiology. INFRAFRONTIER will provide open access to all characterised disease models and phenotyping data.
More information about this call
Mutant mouse technology represents a powerful means to investigate the genetic basis of behavior and to elucidate the mechanisms underlying neurological and psychiatric disorders. PHENOMIN-ICS was able to support three In-depth behavioral phenotyping projects of mouse models through this call.
PHENOMIN-ICS carried out neuro-behavioural phenotyping on 3 projects selected from 9 submitted projects (9 different PI's applications)
The Neurobiology and Behavior platform has developed a battery of tests adapted to the mouse. These tests include analyses of sensory responses, motor abilities, cognitive functions as well as behaviors related to neuropsychiatric disorders, such as anxiety, depression or schizophrenia. Tests may be utilized as a package for phenotyping genetically modified mice or to screen for potential therapeutics. A flow scheme was suggested by experence while it might have been customized upon request from the PI, for a similar final budget.
Precision mammalian model development / rat models
Rat models for studies in neurobiology, cardiobiology, and immunology
Main objective of this INFRAFRONTIER open call is to facilitate access for the wider biomedical research community to the unique infrastructure and scientific expertise of the participating INFRAFRONTIER partners, to deliver novel rat mutant models that will advance knowledge of human disease and will be of widespread use in biomedical science. Many cognitive and physiological characteristics make the rat an ideal human disease model and choice for laboratory studies in neurobiology, cardiobiology, and immunology. Recent advances in genome-editing technology will be used to develop new rat models of human disease.
INFRAFRONTIER will provide open access to all newly developed disease models through the European Mouse Mutant Archive (EMMA). Access to this free-of-charge-service will be granted on the basis of the applicant’s research plans and the potential impact of the proposed novel rat model on the wider biomedical research community.
More information about this call
PHENOMIN-ICS carried out 2 projects of new rat models generation amongst 6 submitted from 6 different PIs.
The French Foundation for rare diseases "Fondation maladies rares" and the French National Infrastructure PHENOMIN are pleased to launch their 3rd joint call for the creation and exploration of mouse models for rare diseases.
The call for projects 'Mouse models and rare diseases' aims to give a significant boost to the development of mouse models, in order to:
Indeed, producing these models meets a key objective in the development of a therapeutic strategy. After their initial in vitro testing, therapeutic proofs of concept must be tested in a living model that recapitulates as closely as possible both the phenotype and biological defects associated to the human disease. Such a model should provide appropriate data regarding the safety and the efficiency of the drug, thus evaluating its benefit/risk ratio, prior to conducting early phases of a therapeutic trial. PHENOMIN and the French Foundation for rare diseases combine their efforts in order to achieve these objectives through the joint call for proposals for the generation and characterization of mouse models, dedicated to rare diseases. This action is part of the objectives of PHENOMIN to develop mouse model resources that will be made available to the scientific community.
Upload the call for proposal 2016-MousemodelsRareDiseases-final.pdf
Submission deadline for proposals: February 9, 2017, 5:00 pm
On line submission: HERE.
We are glad to announce the new PHENOMIN call dedicated to generation and characterization of CreERT2 cell specific promoter driven deleter mouse lines.
Since 2011, PHENOMIN has generated more than 150 models with conditional potential. In the frame of the International Mouse Phenotyping Consortium (IMPC) more than 5,000 genes are already committed to the IMPC pipeline. Most of these models can be driven in conditional alleles.
We aim to maximize the utility of this resource by offering the scientific community with the possibility to nominate the making of new Cre or CreERT2 lines.
In the last decade, we have generated and validated more than 30 cell specific inducible CreERT2 deleter lines (http://mousecre.phenomin.fr/). We have written guidelines for using cre/lox system in mice (European FP7 CREATE program, http://www.creline.org/other_cre_db_resources). We developed a highly efficient universal cre deleter line (http://www.ncbi.nlm.nih.gov/pubmed/22121025). As a partner in EUCOMTOOLS effort, we are establishing new 250 CreERT2 knock-in models (http://www.mousephenotype.org/about-ikmc/eucommtools) in a pure C57BL/6N background.
The call targets the French scientific community. It is a real opportunity to nominate new CreERT2 drivers with useful expression patterns. Projects will be selected on scientific bases and non-availability of similar Cre/CreERT2 lines available in other repositories. Proposals will be reviewed by a scientific committee.
Application deadline is 15th of October 2015.
The National Infrastructure PHENOMIN is pleased to announce the results of its 6th Call: Generation and Characterization of CreERT2 cell specific promoter driven deleter mouse lines. The Scientific Committee has selected 13 projects amongst 34 submitted projects from 20 PI. Consequently, 9 additional CreERT2 mouse lines will be generated by PHENOMIN team and will be made available as soon as possible for the scientific community.
The 9 selected models are based on (in alphabetical order):
4 CreERT2 mouse models have been already generated by the European EUCOMMTOOLS consortium and will be further characterized (in alphabetical order):
To get more information, contact mutagenesis@igbmc.fr
Thanks again to all the participants !
We are glad to announce the 5th PHENOMIN call for proposals for conditional or constitutive knock-out mouse generation and standard phenotyping.
Since 2011, PHENOMIN has generated more than 150 models. In the frame of the International Mouse Phenotyping Consortium (IMPC) more than 5,000 genes are already committed to the IMPC pipeline.
Until the end of 2016, PHENOMIN will generate 100 additional knock-out lines. All these lines will be phenotyped through the standardized IMPC broad-based pipeline.
Up to now, all models have been generated from ES mutant cells with conditional potential generated by the International Knockout Mouse Consortium (IKMC).
In the frame of this 5th call, we have added constitutive knock-out models to be generated using CRISPR (clustered regularly interspaced short palindromic repeats) genome editing technology.
Conditions for eligibility:
For all models that will be selected, please consider that:
The National Infrastructure PHENOMIN is pleased to announce the 5th Call for Proposals results for conditional or constitutive knock-out mouse generation and standard phenotyping. For the first time, the use of the CRISPR/Cas9 technology was included (KO models only).
Following the strong success of previous calls (more than 440 proposal submissions), the French academic scientific community has renewed its interest for phenogenomics.
The Scientific Committee has selected 39 projects amongst 46 submitted projects from 32 PIs.
Thanks to all scientists for your continuous interest.
The French fondation for rare diseases "Fondation maladies rares" and the National Infrastructure PHENOMIN are pleased to announce the launch of the 2nd call for joint research projects: "Mouse models and rare diseases".
This call for projects 'Mouse models and rare diseases' aims to give a significant boost to the development of mouse models, in order to :
Indeed, producing these models meets a key objective in the development of a therapeutic strategy. After their initial in vitro testing, therapeutic proofs of concept must be tested in a living model that recapitulates as closely as possible both the phenotype and biological defects associated to the human disease.
Such a model should provide appropriate data regarding the safety and the efficiency of the drug, thus evaluating its benefit/risk ratio, prior to conduct early phases of a therapeutic trial.
Full text of the call for projects (PDF) (453.4 KB)
Application form (Word) (227.5 KB)
You can also download these documents from the website of the Foundation for rare diseases (http://fondation-maladiesrares.org) by registering / logging in professional area, Call Projects section.
Research projects must be submitted via filled application form no later than January 13, 2015 5:00pm:
Each submitted form must be related to only one model.
We remain at your disposal for any further information and hope that you will respond to this call for many projects.
Wishing you every success in your projects.
The "Fondation maladies rares" in partnership with the National Infrastructure PHENOMIN, is supporting 13 research projects focusing on the development and the study of mouse models in the field of rare diseases.
The Joint Call "Mouse models and rare diseases" aims to give a significant impetus to the creation and the study of mouse models for rare diseases in order to elucidate underlying pathophysiological mechanisms and to develop new therapeutic approaches. This joint call is dedicated to the creation and the characterization of mouse models for rare diseases - constitutive Knock-Out (KO) / conditional Knock-Out (cKO), Knock-In (KI) and transgenic mice.
Platforms of PHENOMIN infrastructure which are partners of that Joint Call:
We are glad to announce the 3rd PHENOMIN expressions of Interest for generation and characterization of transgenic mouse lines bearing a single gene knock-out (with conditional potential).
Today, through its partnership with the International Mouse Phenotyping Consortium (IMPC) PHENOMIN has generated nearly 150 models and more than 5.000 genes are already committed to the pipeline of the IMPC.
The National Infrastructure PHENOMIN is pleased to announce the results of the 3rd Call for Proposals 2013: Establishing and characterizing mouse models - conditional Knock-Out (cKO).
The Scientific Committee has selected 45 projects amongst 98 submitted projects from 59 PI.
Consequently, 45 additional new mouse lines will be generated by PHENOMIN team, in order to be available as soon as possible for the scientific community.
The French fondation for rare diseases "Fondation maladies rares" and the National Infrastructure PHENOMIN are pleased to announce the launch the call for joint research projects: "Murine models and rare diseases".
This call for proposals aims to establish and characterize mouse models: conditional Knock-Out (cKO), Knock-In (KI) and transgenic (TG) in the field of rare diseases. These knockout mice, together with the wealth of associated data, will serve as a valuable, freely available, resource for French researchers investigating gene function and human pathophysiology.
Full text of the call for projects (PDF) (453.4 KB)
Application form (Word) (199.0 KB)
You can also download these documents from the website of the Foundation for rare diseases (http://fondation-maladiesrares.org) by registering / logging in professional area, Call Projects section.
Research projects must be submitted via filled application form no later than Thursday, February 28, 2013:
We remain at your disposal for any further information and hope that you will respond to this call for many projects.
Wishing you every success in your projects.
The "Fondation maladies rares" and the National Infrastructure PHENOMIN are pleased to announce the results of the Call for Proposals 2013 for joint research projects "Murine models and rare diseases". The ad hoc Scientific Committee ("Fondation Maladies Rares" - PHENOMIN) has selected 20 projects amongst 60 submitted projects.
Congratulations to the laureates!
List of selected projects (PDF) (61.0 KB)
Through its partnership in the IMPC, PHENOMIN will, over the next 5 years, produce over 300 transgenic mouse lines bearing a single gene knock-out and analyse them using broad-based, high-throughput phenotyping. This first call for proposal marks the beginning of this strong partnership.
These knockout mice, together with the wealth of associated data, will serve as a valuable, freely available, resource for French researchers.
249 genes were nominated by 85 French PI. Using two selection criterias (value of the scientific project and availability of at least 3 clones with conditional potential in the ES mutant cells resources (International Knockout Mouse Consortium - IKMC)), we were able to select 140 genes which enter the process of mouse model production and phenotyping.
Consequently, additional new mouse lines have been generated by PHENOMIN.