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The National Library of Medicine (NLM) is pleased to announce applications are open to its Michael E. DeBakey Fellowship in the History of Medicine. The NLM Michael E. DeBakey Fellowship in the History of Medicine provides selected individuals with

The National Library of Medicine (NLM) is pleased to announce applications are open to its Michael E. DeBakey Fellowship in the History of Medicine. The NLM Michael E. DeBakey Fellowship in the History of Medicine provides selected individuals with

Eugene V. Koonin, Ph.D., senior investigator at the National Library of Medicine’s (NLM’s) National Center for Biotechnology Information, has been appointed an NIH Distinguished Investigator.

Eugene V. Koonin, Ph.D., senior investigator at the National Library of Medicine’s (NLM’s) National Center for Biotechnology Information, has been appointed an NIH Distinguished Investigator.

We will begin evaluating applications on April 09, 2021. Applications will be accepted until the position is filled.

We will begin evaluating applications on April 09, 2021. Applications will be accepted until the position is filled.

Eugene V. Koonin, PhD, senior investigator in the Computational Biology Branch of the NLM Intramural Research Program, has been elected to the National Academy of Medicine (NAM). The announcement was made today as part of NAM’s annual meeting.

Eugene V. Koonin, PhD, senior investigator in the Computational Biology Branch of the NLM Intramural Research Program, has been elected to the National Academy of Medicine (NAM). The announcement was made today as part of NAM’s annual meeting.

A team of researchers from the National Library of Medicine (NLM) at the National Institutes of Health (NIH) and the Broad Institute developed an improved web-based system, LitVar 2.0, to help researchers and clinicians search for genetic variants

A team of researchers from the National Library of Medicine (NLM) at the National Institutes of Health (NIH) and the Broad Institute developed an improved web-based system, LitVar 2.0, to help researchers and clinicians search for genetic variants