您可通过产品选择器寻找最适合您应用的相关QIAGEN产品。请从以下类别选择。

12 个查询结果

GeneGlobe Data Analysis Center
For analyzing and interpreting real-time PCR or NGS data
    • Intuitive, user-friendly interface with no bioinformatics skills needed
    • Complimentary data analysis for all GeneGlobe assays and arrays
    • Get results in scatter plot, volcano plot, clustergram and heat map formats
CentoMD
For research use, clinical reporting or clinical diagnostic purposes
ANNOVAR
ANNOVAR
CLC Assembly Cell
A high-performance computing solution for mapping reads to a reference and de novo ...
    • Read mapping of Illumina, Pacific Biosciences, Ion Torrent, SOLiD, and 454 sequencing data

    • De novo assembly of Illumina, Pacific Biosciences, Ion Torrent and 454 sequencing data

    • Support for both short read and long read assembly and mapping

Ingenuity Pathway Analysis (IPA)
适用于'omics数据建模、分析和理解
    • 基因表达/miRNA/SNP微阵列数据分析
    • 更深入地理解代谢组学、蛋白质组学和RNAseq数据
    • 上游调节因子鉴定
    • 深入理解分子和化学相互作用以及细胞表型
    • 疾病进程相关的发现
HGMD

The gold standard resource for comprehensive data on published human inherited disease ...

    • 220,000+ mutation reports including specifics on genome coordinates, sequence details, and links to the source reference as well as public resources like dbSNP and OMIM
    • 8,000+ summary reports listing all known inherited disease mutations for a given gene characterized by six different pathogenic variant classes
    • Advanced search functionality, including the ability to find mutations based on the type of nucleotide or amino acid change, or their location in a specific motif, splice site, or regulatory region

     

CLC Main Workbench
用于高级DNA、RNA和蛋白分析
    • 用于高级DNA、RNA和蛋白分析的综合性工作平台
    • 直观的图形用户界面
    • 支持同事和合作者之间高效分享数据
    • 经常更新最新的科学发展成果
Workbench Modules
For enhancing functionalities of CLC Genomics Workbench, Biomedical Genomics Workbench, ...
    • The modules have an intuitive and user-friendly interface
    • They incorporate cutting-edge technology and algorithms
CLC Genomics Server
For flexible next-generation sequencing data analysis
    • Central execution platform with flexible queuing system
    • Maximum client-flexibility with support for CLC Genomics Workbench
    • Highly customizable on both client- and server-side
    • Advanced and customizable data import/export framework
    • Central data storage
CLC Genomics Cloud Engine
CLC Genomics Cloud Engine
Ingenuity Variant Analysis
适用于从人全基因组、外显子组和基因检测板二代测序研究中鉴定致病性变异
    • 使用方便且直观的界面,无需生物信息学技巧
    • 互动式过滤缩小了变异搜索范围
    • 基于网络的应用程序可与HIPAA和Safe Harbor标准兼容
    • 用于合作和稿件准备的共享和发表工具
CLC Genomics Workbench
用于二代测序数据的分析、对比和可视化
    • 直观友好的界面,适用于多平台应用
    • 整合了先进的技术和算法
    • 涵盖遗传学、转录组学和表观遗传学所需的众多功能
    • 支持多种主要的二代测序仪