Recent blog posts
We have re-annotated all RefSeq genomes for Escherichia coli, Mycobacterium tuberculosis, Bacillus subtilis, Acinetobacter pittii, and Campylobacter jejuni using the most recent release of PGAP. You will find that more genes now have gene symbols (e.g. recA). Your feedback indicated that the lack of symbols was an impediment to comparative analysis, so we hope that this improvement … Continue reading Announcing the re-annotation of RefSeq genome assemblies for E. coli and four other species!
Guest post by Carolina Mendoza-Puccini, MD, CDE Program Officer, Division of Clinical Research, National Institute of Neurological Disorders and Stroke (NINDS) and Kenneth J. Wilkins, PhD, Mathematical Statistician, Biostatistics Program and Office of Clinical Research Support, Office of the Director, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Previous posts published in Musings … Continue reading "Common Data Elements: Increasing FAIR Data Sharing"
Join us on June 30, 2021 at 12PM eastern time to learn how to use the new NCBI Datasets resource to find and download gene, genome and SARS-CoV-2 sequence and annotation. You will learn how to access these datasets through either the web interface or the new command-line tools that allow you to incorporate these data … Continue reading June 30 Webinar: Using NCBI Datasets to download sequence and annotation for genomes and genes
The White House wants to fight climate change in ways that also remove economic and racial disparities. The city of Cleveland has a plan that describes what that might mean.
Going to bed early and waking up early may help to provide some protection against depression, a new study suggests.
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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
Genome sequence assemblies, large-scale functional genomics data, and source biological samples
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Heritable DNA variations, associations with human pathologies, and clinical diagnostics and treatments
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Short genetic variations
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Online mendelian inheritance in man
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