View the complete HGMD Professional statistics here.
When using Batch Search, the results table will now include a ClinVar column to the far right. This column will provide links to ClinVar records and list predicted classifications.
Read about the importance of having access to the most up-to-date and comprehensive database for human disease mutations in our white paper.
Learn how to take advantage of all HGMD’s features by watching our video tutorials available at our Resources Page.
New ANNOVAR databases are now available!
Learn more about how ANNOVAR can be used with HGMD for variant annotation.
Watch a recorded webinar featuring ANNOVAR here.
Genome Trax 2018.4 has updated tracks containing the 2018.4 HGMD release or all HGMD-related tracks.
Need a clinical genomic interpretation solution?
Look no further than QIAGEN Clinical Insight (QCI). Offering the highest level of interpretation transparency currently available on the market, QCI dynamically computes ACMG classification and AMP-tiering based on phenotype and clinical evidence. QCI incorporates knowledge from HGMD, CentoMD, over 30 public and proprietary databases, and over 2,000 scientific and clinical articles manually curated each month.
Kick start your year and sign-up for a free QCI demo here!