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Agilent NGS Genomics Solutions Workflow Infographic
- 文件出版號: 5994-6049EN
- 創(chuàng)建日期: 20 四月 2023
- 9 MB
Shariant case study
- 文件出版號: 5994-5041EN
- 創(chuàng)建日期: 10 六月 2022
- 379 KB
Updated Datasheet for Alissa Interpret v5.4
- 文件出版號: 5991-8498EN
- 創(chuàng)建日期: 16 五月 2022
- 2 MB
How customers have established their laboratories' routine testing on the Alissa Clinical Informatics Platform.
- 文件出版號: PR7000-0746 / 5991-8535EN
- 創(chuàng)建日期: 30 七月 2019
- 844 KB
An automated pipeline for NGS testing and reporting in a commercial molecular pathology lab.
- 文件出版號: 5991-9205 replaces 5991-8529EN
- 創(chuàng)建日期: 30 七月 2019
- 596 KB
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.
- 文件出版號: 5991-9111EN
- 創(chuàng)建日期: 30 七月 2019
- 1 MB
Assessment of the performance of Alissa Align & Call and four other common variant callers on SNPs in a normal diploid sample,
- 文件出版號: 5994-0169EN
- 創(chuàng)建日期: 29 七月 2019
- 2 MB
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.
- 文件出版號: 5991-8530EN
- 創(chuàng)建日期: 01 七月 2019
- 700 KB
How UMC Utrecht implemented an automated and tiered approach for Whole Exome Sequencing (WES) diagnostics using Alissa Interpret.
- 文件出版號: 5991-8533EN
- 創(chuàng)建日期: 01 七月 2019
- 1 MB
Alissa Interpret | Research, the next evolution of Cartagenia Bench, allows clinical research labs to efficiently triage, curate and report genomic variants.
- 文件出版號: 5991-8840EN
- 創(chuàng)建日期: 09 三月 2018
- 2 MB