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必威体育登录手机The Agilent Alissa Reporter platform is an intuitive and streamlined cloud-based NGS secondary analysis software-as-a-service solution.
- Publication Part Number: 5994-4282EN
- Created: 19 June 2024
- 4 MB
Offers customized genomic profiling of cancer samples with custom NGS panels, which can incorporate new and emerging biomarkers.Enables assessment of CNVs, SNVs, indels, translocations, TMB, MSI.
- Publication Part Number: 5994-7308en
- Created: 01 Apr 2024
- 1 MB
必威体育登录手机The Agilent Alissa Reporter platform is an intuitive and streamlined cloud-based NGS secondary analysis software-as-a-service solution.
- Publication Part Number: 5994-6507EN
- Created: 01 Feb 2024
- 257 KB
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.
- Publication Part Number: 5994-6577EN
- Created: 05 Jan 2024
- 1 MB
必威体育登录手机Automation of the Agilent SureSelect XT HS2 library preparation workflow on the Agilent Magnis NGS Prep system.
- Publication Part Number: 5994-4951en
- Created: 08 Sep 2023
- 505 KB
Offers tumor-specific profiling of lung, colon, pancreas, kidney, and bladder with NGS panels of globally curated genes sourced from cancer databases.Enables detection of CNVs, SNVs, indels, translocations.
- Publication Part Number: 5994-6687EN
- Created: 07 Sep 2023
- 508 KB
必威体育登录手机The Agilent SureSelect XT HS2 DNA reagent kit is a state-of-the-art NGS library preparation and target enrichment solution.It provides a streamlined and flexible workflow, excellent performance, and comprehensive features that can be used in...
- Publication Part Number: 5994-1687EN
- Created: 05 June 2023
- 312 KB
SureSelect Clinical Focused Exome V4: Whole exome sequencing powered by insights from the genome
- Publication Part Number: 5994-6205EN
- Created: 05 June 2023
- 579 KB
Offers genomic profiling of cancer samples with a NGS panel of globally curated genes sourced from cancer databases.Enables detection of CNVs, SNVs, indels, translocations, gene fusions as well as TMB & MSI.
- Publication Part Number: 5994-5796EN
- Created: 01 Mar 2023
- 2 MB
Datasheet for the Magnis SureSelect XT HS2 RNA reagent kit
- Publication Part Number: 5994-5823EN
- Created: 24 Feb 2023
- 376 KB
Data sheet for automation of SureSelect XT HS2 DNA on the Bravo NGS workstation with the on-deck thermal cycler (ODTC).
- Publication Part Number: 5994-5787EN
- Created: 15 Feb 2023
- 409 KB
Somatic and Germline sequencing of SureSelect Libraries on the Element AVITI System
- Publication Part Number: 5994-4647EN
- Created: 04 Mar 2022
- 480 KB
Library Preparation Performance on the Magnis NGS Prep System with Reagent and Protocol Updates
- Publication Part Number: 5994-3865EN
- Created: 27 Aug 2021
- 265 KB
SureSelect Human All Exon V8 Datasheet: High Performance Exome Built on Advanced and Proven Technology
- Publication Part Number: 5994-3154EN
- Created: 21 July 2021
- 869 KB
必威体育登录手机"The Agilent SureSelect XT HS2 RNA Reagent Kit is an advanced solution for targeted RNA-Seq.It is optimized for low-input, formalin-fixed paraffin-embedded (FFPE) samples, a critical sample type for translational cancer research."
- Publication Part Number: 5994-2314EN
- Created: 17 Aug 2020
- 252 KB
必威体育登录手机The Agilent Magnis NGS Prep System (Figure 1) produces sequencing-ready libraries compatible with Illumina platforms.It is comprised of an instrument, reagents, and pre-configured protocols.The system is fully automated to deliver eight libraries...
- Publication Part Number: 5994-1624EN
- Created: 20 Feb 2020
- 1 MB
Alissa Align & Call ushers in the next generation of NGS data analysis, delivering bioinformatic accuracy and speed, from raw data to draft report
- Publication Part Number: 5991-9121EN
- Created: 27 Jan 2020
- 2 MB
SureSelect Cancer All-in-One solid tumor assay enables the detection of SNVs, indels, CNVs and translocations in genes relevant to common tumor types.This assay requires a single genomic DNA and is compatible with FFPE tumor samples.
- Publication Part Number: 5994-1005EN
- Created: 22 May 2019
- 589 KB
One assay, all lung cancer-relevant variants in a single DNA workflow
- Publication Part Number: 5994-0231EN
- Created: 04 Dec 2018
- 925 KB
NGS with Molecular Barcodes Uncovers Somatic Mosaicism
- Publication Part Number: 5991-6886EN
- Created: 30 Nov 2018
- 288 KB