Events
EHA
Online: June 9-17 2021
ESHG 2021
Online: August 28-31 2021
PMWC 2021 Silicon Valley
Online: June 14-18 2021
Consolidated approach for the interpretation of hereditary cancer variants
Online: June 22 2021
Medlab Middle East
Online: 23 May-22 July 2021 & In person: 21-24 June 2021
RCPA Pathology Update
In person: 2-4 July 2021
CGC
Online: August 1-4 2021
HGSA
In person: 4-17 August 2021
HLTH
In person: October 17-20 2021
RSNA
In person: November 28 - December 2 2021
AMP
In person: November 16-20 2021
Past Events
Implementation of a customized myeloid NGS-based solution in an academic clinical laboratory
The University of Michigan implemented a new NGS capture-based solution to assess myeloid malignancies.
A streamlined workflow for CNV analysis on whole-exome sequencing
Whole-exome sequencing has emerged as a comprehensive and cost-effective tool for researching rare disease-causing variants.
SOPHiA DDM™ platform and Microsoft Azure for genomics: When accuracy meets security
The SOPHiA DDM™ platform unlocks the power of new-generation health data for cancer and rare disease management.
Advanced germline variant analysis with the SOPHiA DDM™ platform
A major challenge in precision medicine is quick, reliable identification of potentially disease-causing genetic variants.
