February 6 Webinar: New Variation Services for Normalizing, Remapping, and Annotating Variants | NCBI Insights

February 6 Webinar: New Variation Services for Normalizing, Remapping, and Annotating Variants | NCBI Insights

February 6 Webinar: New Variation Services for Normalizing, Remapping, and Annotating Variants

01/16/2019 02:14 PM EST

Join us on Wednesday, February, 2019, when NCBI staff will show you how to use a new set of NCBI variation services that rely on a variant data model called SPDI (Sequence Position Deletion Insertion). These services and data model allow … Continue reading →

NLM Technical Bulletin, Nov-Dec 2018, MeSH Webinars: 2019 Highlights and PubMed Searching in January 2019 [Editor's Note Added]

01/16/2019 01:39 PM EST

A recording of the 2019 MeSH Highlights Webinar is available.

RefSeq release 92 updates 10,000 human transcripts

01/16/2019 01:09 PM EST

RefSeq release 92 is accessible online, via FTP and through NCBI’s Entrez programming utilities, E-utilities. This full release incorporates genomic, transcript, and protein data available, as of January 4, 2019 and contains 185,738,687 records, including 130,366,644 proteins, 25,088,890 RNAs, and … Continue reading →

NLM’s 2019 In/Out List

01/16/2019 09:00 AM EST

We made it! Another year is upon us, and with it, a sense of anticipation for what’s to come. We’re not those who can just wait for time to tell its tale, however, so we’ve put on our prognosticator’s hat, peered into the future, and come up with our list of what’s in for the…