Using Ncbi Data With Tools That Predict The Functional Impact Of Genomic Variants

Using NCBI Data with Tools that Predict the Functional Impact of Genomic Variants

National Library of Medicine

Using NCBI Data with Tools that Predict the Functional Impact of Genomic Variants

National Library of Medicine

Webinar: NCBI Resources and Variant Interpretation Tools for the Clinical Community

National Library of Medicine

The NCBI Minute: Find All Variants with ClinVar

National Library of Medicine

How to Use the NCBI’s Bioinformatics Tools and Databases

Science Buddies

Analyzing Gene Sequence Results with BLAST

Catalyst University

How to Search ClinVar

ClinGen Resource

NCBI Minute: Using NCBI Datasets Command-line Tools to Access Data and Metadata for Genomes

National Library of Medicine

Interactive Visualization of NCBI Annotations for Variant Interpretation

National Library of Medicine

Predicting the Deleteriousness of Genomic Variants – Big and Small

Simons Institute

Introducing NCBI's Comparative Genome Viewer, CGV

National Library of Medicine

NCBI Minute: Introducing the New RefSeq Functional Elements Project

National Library of Medicine

Webinar: Eukaryotic Genome Data Curation at NCBI

National Library of Medicine

RefSeq and NCBI Gene

ClinGen Resource

Knowing Your NGS Downstream: Functional Predictions

Golden Helix Inc.

Using CATH-Gene3D to predict the structure... - Christine Orengo - Technology Track - ISMB/ECCB 2017

ISCB

NCBI NOW, Lecture 5, More DNA-seq and Basic Variant Analysis

National Library of Medicine

NCBI Minute: NCBI Hackathons, a Framework for Prototyping Pipelines

National Library of Medicine

NCBI Minute: Human Population Genetic Data at NCBI

National Library of Medicine

NCBI Minute: Variant Interpretation Using NCBI Resources

National Library of Medicine