Alamut™ Visual Plus

Pinpoint and visualize pathogenic mutations
Alamut™ Visual Plus equips you to conclude challenging cases by enabling you to see and understand the genomic context of variants.
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Revealing answers for complex conditions

Alamut™ Visual Plus streamlines your workflows by connecting you to curated databases and prediction tools while providing enhanced variant visualization, so you can quickly confirm and report causative variants.
Genomic visualization
The full genome browser reveals previously overlooked variants.
Comprehensive annotation
Variants are annotated with information from renowned databases, missense and splicing predictors, and publications.
Universal add-on
Alamut™ Visual Plus seamlessly enriches any tertiary analysis workflow.

Accelerate variant analysis and interpretation

Comprehensive variant annotation
  • ACMG point-based classification with evidence strength filtering
  • Backed by literature and international guidelines (e.g., Mastermind®, PubMed®, HGVS)
  • Variant annotation from >55 renowned databases (e.g., ClinVar, dbSNP, BRIDGES, COSMIC, dbVar)
  • Missense and splice variant predictors (e.g., REVEL, MaxEntScan, PolyPhen-2‚ NNSPLICE [BDGP]) 
Enhanced variant visualization
  • Comprehensive full-genome browser
  • GRCh37/38 assemblies and mitochondrial genome visualization
  • Structural variant track including copy number variation (CNV) analysis
  • Displays flanking regions and overlapping genes
  • BAM, VCF, BED, and Sanger file viewers
  • Simultaneous exploration of multiple genes
3. Prioritization and filtering
  • Secure login with 2-step verification
  • Quick upload of FASTQ files
  • Performance pipelines tailored to sample type, chemistry, enrichment kit, and sequencer
4. Exploration and Interpretation
  • Secure login with 2-step verification
  • Quick upload of FASTQ files
  • Performance pipelines tailored to sample type, chemistry, enrichment kit, and sequencer
Efficient laboratory workflows
  • Add-on to any workflow
  • Data management
  • Direct link from SOPHiA DDM™
  • Dynamic variant filtering
  • Customizable reporting

Navigate genomic data

SOPHiA DDM™ and Alamut™ Visual Plus are your co-pilots for navigating complex genomic data.

Gain deeper insights into challenging genomic variants with enhanced variant annotation and prioritization powered by SOPHiA DDM™ and
Alamut™ Visual Plus.
WATCH THE WEBINAR
Seamlessly integrate Alamut™ Visual Plus into workflows utilizing leading sequencers, secondary and tertiary analytics.
Associate variants with individual-specific HPO terms and track variant occurrences and history for re-analysis.
Access Alamut™ Visual Plus through SOPHiA DDM™ or as a stand-alone software.

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SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.

SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us at [email protected] to obtain the appropriate product information for your country of residence.

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SOPHiA DDM™ Overview
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SOPHiA DDM™ for Genomics

Oncology 

Rare and Inherited Disorders

Add-On Modules

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Unlock entirely novel insights from your radiology images
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SOPHiA DDM™ for Multimodal
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