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必威体育登录手机Agilent now provides a WES solution for cancer research labs that includes exome enrichment reagents and software for variant analysis and interpretation.
Updated Datasheet for Alissa Interpret v5.4
Alissa Align & Call ushers in the next generation of NGS data analysis, delivering bioinformatic accuracy and speed, from raw data to draft report
An automated pipeline for NGS testing and reporting in a commercial molecular pathology lab.
Alissa Interpret | Research, the next evolution of Cartagenia Bench, allows clinical research labs to efficiently triage, curate and report genomic variants.
| Spanish (Mexico) | Complete (PDF) |
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| Portuguese (Brazil) | Complete (PDF) |
This white paper explains how the Alissa Clinical Informatics Platform implements security measures.
必威体育登录手机Agilent provides a whole exome sequencing solution for genetics labs.
必威体育登录手机Agilent NGS Genomics Solutions Workflow Infographic
Shariant case study
UMC Utrecht Genetics uses Alissa to build a foundation to efficiently transition to whole genome sequencing with combined CNV and SNV analysis on the same data set.
How customers have established their laboratories' routine testing on the Alissa Clinical Informatics Platform.
Assessment of the performance of Alissa Align & Call and four other common variant callers on SNPs in a normal diploid sample,
Learn how Robert-Debré hospital saves time by using Alissa Interpret to set up a variant classification strategy to help diagnose patients suffering from rare dev pathologies.
How UMC Utrecht implemented an automated and tiered approach for Whole Exome Sequencing (WES) diagnostics using Alissa Interpret.