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1 - 16 共 16 條結(jié)果
應(yīng)用的篩選條件
我們的 Alissa 臨床信息學(xué)平臺(tái)提供了創(chuàng)新型 NGS 和 CGH 數(shù)據(jù)分析、變異解析和臨床級(jí)報(bào)告起草模塊，并針對(duì)各種技術(shù)和應(yīng)用的工作流程進(jìn)行了優(yōu)化。
Align & Call 為 NGS 信息學(xué)提供二級(jí)分析工作流程，可用于原始數(shù)據(jù)和 VCF 文件。
Agilent now provides a WES solution for cancer research labs that includes exome enrichment reagents and software for variant analysis and interpretation.
Agilent provides a whole exome sequencing solution for genetics labs.
Agilent NGS Genomics Solutions Workflow Infographic
Shariant case study
Updated Datasheet for Alissa Interpret v5.4
How customers have established their laboratories' routine testing on the Alissa Clinical Informatics Platform.
An automated pipeline for NGS testing and reporting in a commercial molecular pathology lab.
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.
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.
Alissa Interpret | Research, the next evolution of Cartagenia Bench, allows clinical research labs to efficiently triage, curate and report genomic variants.
The Alissa Clinical Informatics Platform offers integrated sequencing analysis solutions.