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Gene sequences and annotations used as references for the study of orthologs structure, expression, and evolution
Protein sequences, 3-D structures, and tools for the study of functional protein domains and active sites
A tool to find regions of similarity between biological sequences
Genome sequence assemblies, large-scale functional genomics data, and source biological samples
Genome assembly information
Museum, herbaria, and other biorepository collections
Biological projects providing data to NCBI
Descriptions of biological source materials
Genome sequencing projects by organism
DNA and RNA sequences
High-throughput sequence reads
Taxonomic classification and nomenclature
Heritable DNA variations, associations with human pathologies, and clinical diagnostics and treatments
Privately and publicly funded clinical studies conducted around the world
Human variations of clinical significance
Genotype/phenotype interaction studies
Short genetic variations
Genome structural variation studies
Genetic testing registry
Medical genetics literature and links
Online mendelian inheritance in man
Repository of chemical information, molecular pathways, and tools for bioactivity screening
Pharmacy closures and layoffs by two large home infusion companies spark fears for those who require parenteral nutrition.
Keeping a child home from school for “cognitive rest” after a concussion may do more harm than good, according to a study.
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Do you currently add an organism name(s) to focus your searches when using the BLAST standard nr database? You can now focus your searches by organism with the BLAST ClusteredNR database and get faster results with a better overview of protein homologs in a wider range of organisms. Your searches will be restricted to protein … Continue reading Now Available! Add your favorite organism(s) to your BLAST ClusteredNR searches
The NIH’s All of Us Research Program is a historic effort to create an unprecedented research resource that will speed biomedical breakthroughs, transform medicine and advance health equity. To create this resource, we are enrolling at least 1 million people who reflect the diversity of the United States.
Do you work with human-derived sequence data? Do you often struggle with the need to determine if your data is free of human sequence and therefore suitable for public distribution? We encourage submitters to screen for and remove contaminating human reads from data files prior to submission to SRA. To support investigators in this effort, … Continue reading Scrubbing human sequence contamination from Sequence Read Archive (SRA) submissions