SOPHiA DDM™ PLATFORM

SOPHiA DDM™ PLATFORM

SOPHiA DDM™ PLATFORM

It eases the data analysis without having prior knowledge about bioinformatics.

SOPHiA DDM™ uses machine learning with patented algorithms for variants pre-classification from raw data.

For a demo of the SOPHiA DDM™ platform in five simple steps, click here.

Unique and ideal platform for the interpretation of genomic data.

  • User-friendly browser interface.
  • Analysis, selection, and variants filtering.
  • Didactic and dynamic visualization of data.
  • Easy report generation.
  • Artificial intelligence algorithms.
  • Regular database updates.
  • SOPHiA Community feedback.
  • Multimodal integration of patient data.

ANALYTICS

GRCh38/hg38 for precise variant annotation.

Dual variants

ACMG implementation and predictions based on machine learning.

Virtual Solution

Updated and trusted databases, such as OMIM and HPO.

Cascading Filters

Filtering options for a quick variant screening.

CNV INTEGRAL DETECTION

Copy Number Variation (CNV) is a genetic risk factor for a lot of disorders.

The SOPHiA DDM™ platform filters data sets of noisy NGS to support precise CNV detection with an exon-level resolution.

ALAMUT™ VISUAL PLUS

Alamut™ Visual Plus allows connecting associations in a genetic scale within a full genome browser for selected databases and splice predictors renowned worldwide.

The intuitive interface allows the visualization of GRCh37/38, or the mitochondrial genome, conveniently displaying regions close to the genes of interest and the choice to see overlapping genes.

Alamut™ Visual Plus

Full genome browser that integrates multiple genomic and curated databases, guides, predictors missense, and splice variants.

Through the ISO 27001 international standard, SOPHiA DDM™ is designed to protect the privacy and integrity of its data with security protocols.

CASCADING FILTERS

SOPHiA DDM™ has intuitive filtering of pathological variants with prioritization methods to speed up the interpreting process.

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SOPHiA GENETICS
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