Category Archives: SPDI
NCBI on YouTube: Get the most out of NCBI resources with these videos
Check out the latest videos on YouTube to learn how to best use NCBI graphical viewers, SRA, PGAP, and other resources. Genome Data Viewer: Analyzing Remote BAM Alignment Files and Other Tips This video shows you how to upload remote … Continue reading
Posted by 1000 Genomes, API, ClinVar, dbgap, dbGaP Allele Frequency Aggregator (ALFA), dbSNP, DNA-Seq, ExAC, GDV, Genome, Genome Data Viewer, GnomAD, human variant data, PGAP, prokaryotic genome annotation, RNA-Seq, SPDI, SRA, TopMed, What's New, youtube
inNCBI on YouTube: Get the most out of NCBI resources with these videos
Check out the latest videos on YouTube to learn how to best use NCBI graphical viewers, SRA, PGAP, and other resources. Genome Data Viewer: Analyzing Remote BAM Alignment Files and Other Tips This video shows you how to upload remote … Continue reading
Posted by 1000 Genomes, API, ClinVar, dbgap, dbGaP Allele Frequency Aggregator (ALFA), dbSNP, DNA-Seq, ExAC, GDV, Genome, Genome Data Viewer, GnomAD, human variant data, PGAP, prokaryotic genome annotation, RNA-Seq, SPDI, SRA, TopMed, What's New, youtube
inFebruary 6 Webinar: New Variation Services for Normalizing, Remapping, and Annotating Variants
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