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AllSeq’s Conference Lists are continually updated lists, overviews and access points for scientific conferences, that allows you to know what conferences are going on where and when. Furthermore, and in collaboration with more of the conferences AllSeq offers discount codes for the conference ticket and other benefits for when you are about to determine which […]
Eurofins Genomics - Genomic services by experts
Genomic services by experts: NGS, genotyping, gene expression, sanger sequencing, oligonucleotides and gene synthesis ** SARS-CoV-2 research support
Eurofins Genomics - Genomic services by experts
Genomic services by experts: NGS, genotyping, gene expression, sanger sequencing, oligonucleotides and gene synthesis ** SARS-CoV-2 research support
Natioanl Institute of Plant Genome Research - Academia.edu
Natioanl Institute of Plant Genome Research on academia.edu
ABOUT US
The National Institute of Plant Genome Research is an autonomous institution supported by the Department of Biotechnology, Government of India. The Institute has been established to coincide with the 50th anniversary of India's independence as well as birth anniversary of Prof. (Dr.) J. C. Bose.
New York Genome Center - A Nonprofit Academic Research Institution
NYGC is nonprofit academic research institution focused on furthering genomic research for neurodegenerative disease, neuropsychiatric disease, and cancer.
The Translational Genomics Research Institute (TGen)
The Translational Genomics Research Institute (TGen) is a non-profit 501(c)(3) organization focused on developing earlier diagnostics and smarter treatments. Translational genomics research is a relatively new field employing innovative advances arising from the Human Genome Project and applying them to the development of diagnostics, prognostics and therapies for cancer, neurological disorders, diabetes and other complex diseases.
Rare and Undiagnosed Network
To empower rare & undiagnosed patients and their families with genomic information and community through advocacy, networking and support.
CIGM - Clinical institute of genomic medicine
Clinical institute of genomic medicine NIPT - An analysis is possible from the 11th week of pregnancy At the Clinical institute of genomic medicine we also offer a non-invasive prenatal test (NIPT) - a test that determines with a high degree of
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REWRITING LIFE | The Chew Lab @ Genome Institute of Singapore
The Chew Lab @ Genome Institute of Singapore
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Rare Disease Database, Rare Disease Conditions, Federated Data Sharing
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Rare Renal | The UK Kidney Association
It is often hard to find detailed information on rare diseases because they affect so few patients. Doctors may only treat a few patients with a rare disease in their whole career. This site aims to provide information and links to 27 different rare renal conditions and their current activity such as patient support groups and research. Please contact us if you are interested
Home - Australian Functional Genomics Network (AFGN)
network of clinicians, diagnostic labs, and researchers investigating pathogenic mechanisms of genes and variants identified in patients with rare diseases and cancers
Other sites like raregenomics org
Home | Rare Diseases Clinical Research Network
The Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research, NCATS, is made up of 21 disease research groups (consortia) and a Data Management and Coordinating Center that work together to improve availability of rare disease information, treatment, clinical studies, and general awareness for both patients and the medical community.
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ERN-LUNG | Rare Respiratory Diseases
WELCOME TO ERN-LUNG ERN-LUNG is a patient-centric network of European healthcare providers and patient organisations, committed Europe-wide and globally to reducing morbidity and mortality from rare lung diseases in people of all ages through patient care, advocacy, education, research and knowledge-sharing. A non-profit project of building a clinical care network for all rare diseases of the respiratory
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Rare Disease Foundation
The Rare Disease Foundation is on a mission to find cures and treatments through its innovative patient-centric approach to research. The Foundation also funds and operates programs that provide resources through community and clinical support channels.
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Rare Diseases: Genetics and Metabolism – MRGM Research aims to decipher the molecular mechanisms laying at the root of the physiopathology o
MRGM Research aims to decipher the molecular mechanisms laying at the root of the physiopathology of rare diseases and make our findings worth for patients.
Diving into Genetics and Genomics
A wet-dry hybrid biologist's take on genetics and genomics. Mostly is about Linux, R, python, reproducible research, open science and NGS. I am working on single-cell transcriptomics at Dana-Farber Cancer Institute. I started a new blog http://divingintogeneticsandgenomics.rbind.io/
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Endo-ERN | European Reference Network on Rare Endocrine Conditions
Endo-ERN , European Reference Network on Rare Endocrine Conditions, European Reference Network on Rare Endocrine Conditions. Endo-ERN’s mission is to reduce and ultimately abolish inequalities in care for patients with rare endocrine disorders in Europe, through facilitating knowledge sharing and facilitating related healthcare and research.
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Support for patients with chronic illness or rare disease
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The European Genome-phenome Archive (EGA) is a service for permanent archiving and sharing of all types of personally identifiable genetic and phenotypic data resulting from biomedical research projects. The EGA contains exclusive data collected from individuals whose consent agreements authorise data release only for specific research use or to bona fide researchers. The EGA provides the necessary security required to control access, and maintain patient confidentiality, while providing access ...
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WIRRED - Walkers Institute For Regenerative Research and Design is a organisation that individuals can connect and reconnect with ecosystems.
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Home | Protect ERNs
What are European Reference Networks? European Reference Networks (ERNs) connect patients, clinicians and researchers across Europe. They allow knowledge and expertise about rare diseases to be shared across Europe; providing patients with access to diagnosis and transformative care, without the burden of long-distance travel. ERNs enable researchers to engage rare disease patients across
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Changing the game - The Nathan Project for Rare Diseases
Kids with rare diseases often fall through the cracks of healthcare systems, causing serious problems for patients, their families, and the doctors who treat them. We are developing a needs assessment tool to help doctors and researchers find and fix these gaps, transforming the lives of these families. Left: Our ambassador, Nathan Garcia […]
National Institute of Solar Energy : : An autonomous institution of Ministry of New and Renewable (MNRE) – National Institute of Solar Energ
National Institute of Solar Energy(NISE), an autonomous institution of Ministry of New and Renewable (MNRE), is the apex National R&D institution in the field Solar Energy. The Government of India has converted 25 year old Solar Energy Centre (SEC) under MNRE to an autonomous institution in September, 2013 to assist the Ministry in implementing the National Solar Mission and to coordinate research, technology and other related works.
Duan Lab - Functional Genomics Lab at Cornell University
I am tweeting (@ellieduan) About us Dr. Ellie Duan joined the Department of Animal Science at Cornell University in July 2021 as an Assistant Professor of Functional Genomics. We moved to Duan Lab official website at Cornell. Please check the Cornell website for future updates. Our research focused on functional...
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home - FunctionalGenomics
WELCOME TO PAWEL LISOWSKI RESEARCH WEBSITE SOLVING MEDICAL MYSTERIES THROUGH GENOME ENGINEERING TECHNOLOGY Decoding of undiagnosed and rare diseasesHealthcare providers are unable to discover the cause for hundreds mysterious diseases every year. Our research study aims to provide answers for patients and families affected by these undiagnosed conditions. We focus on decoding of unknown and...
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