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

How to Use the NCBI’s Bioinformatics Tools and Databases

Science Buddies

The NCBI Minute: Find All Variants with ClinVar

National Library of Medicine

Analyzing Gene Sequence Results with BLAST

Catalyst University

Introducing NCBI's Comparative Genome Viewer, CGV

National Library of Medicine

How to Search ClinVar

ClinGen Resource

Predicting the Deleteriousness of Genomic Variants – Big and Small

Simons Institute

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

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

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

National Library of Medicine

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

ISCB

Variant Annotation Using RegulomeDB and HaploReg - Jill Moore

National Human Genome Research Institute

Ensuring accurate classification of variants in BRCA1, BRCA2 and HRR genes (2022)

Measuring the Functional Consequences of Large Numbers of Human Genetic Variants - Jay Shendure

National Human Genome Research Institute