The names and addresses of people participating in the Personal Genome Project can be easily tracked down despite such data being left off their online profiles.
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Biotech entrepreneur Stephen Friend shares his thoughts on how cancer researchers can collaborate more effectively to achieve faster progress.
The regulatory body that licenses drugs for use in the European Union is devising a policy that will require the publication of some clinical trial data.
Although fully organized patient-run trials are still few and far between, patients are taking a more active role in clinical research.
Patients are sidestepping clinical research and using themselves as guinea pigs to test new treatments for fatal diseases. Will they hurt themselves, or science?
Non-confirmatory or “negative” results are not worthless.
The largest collection of genetic and medical data in the United States links telomeres and genetic variants to longevity and disease.
Will the recently launched Reproducibility Initiative succeed in cleaning up research and reducing retractions?
Giving researchers access to the health records of 52 million people in England could prove invaluable to biomedical scientists.
Reduced support from the US National Library of Medicine threatens to shut down five popular biological databases.
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