Genomic data analysis software, Alissa Interpret

Features

Clinical Decision Support – External and internal curated variant knowledgebases at your fingertips
Secure SaaS Platform – ISO27001 & ISO13485 Certified
Reduce Turnaround Time – Automated variant interpretation solution accelerates CGH and NGS tertiary analysis
Visualize All Variant Types – One platform for SNVs, InDels, CNVs, LOH, and fusions
Increase Productivity – Integrate with your LIMS and eliminate genomic data analysis bottlenecks
Consortium Functionality – Connect with peers, share knowledge, and improve diagnostic yield
Agnostic Solution – Scale from small panels to exomes and genomes with compatibility to support any assay

Applications

Alissa Interpret for Cancer Analysis

Find the right tool to make informed decisions about your cancer sample in the shortest time. Alissa Interpret accelerates your somatic genomic data interpretation with:

Access to up-to-date clinical findings
Actionable biomarkers, trials and therapies
Tumor/normal analysis

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Alissa Interpret for Inherited Disease Analysis

Identify the causative variant in your sample’s inherited disorder or screen for inherited cancer. Alissa Interpret streamlines your germline genomic data interpretation with:

Phenotype-driven variant prioritization
Filter trees for rapid, transparent variant filtration
Single-platform SNV and CNV interpretation
Classification based on ACMG Guidelines
Familial analysis with modes of inheritance

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Combined CGH and NGS Tertiary Analysis

Integrate multiple modes of data into a single platform to get the complete picture of your sample’s genomic profile. Alissa Interpret enables you to overlay NGS and CGH data to maximize diagnostic yield and achieve a faster turnaround time in urgent cases.

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Literature

Key Literature

Alissa Interpret Datasheet 5991-8498EN

Updated Datasheet for Alissa Interpret v5.4

Brochures
English
07 Jun 2022
2.06 MB
PDF

Australian Genomics Pioneers Clinical Data Sharing

Shariant case study

Case Studies
English
10 Aug 2022
379.26 KB
PDF

Exome Enrichment Using Agilent SureSelect Human All Exon V8 Panel And Agilent Alissa Clinical Informatics Platform

Agilent provides a whole exome sequencing solution for genetics labs.

Flyers
English
22 Jun 2023
1.90 MB
PDF

Data Sheets

Flyers

Support

Supplemental Information

Software Use Agreements

1. This product is governed by the Terms and Conditions of the Terms of Use - Agilent Genomics SW (Exhibit 440) and the Data Processor Agreement, which are available on request from Agilent Technologies and on the Agilent.com website.

2. Intended Use Statement