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Next Generation Sequencing

  • Agilent Technologies Array CGH Platform Assures Quality of Cancer Cell Lines Used in Biomedical Research

    SANTA CLARA, Calif., July 28, 2016

  • Agilent Technologies Launches SureGuide CRISPR Libraries for Functional Genomics

    SureGuide Offerings Include GeCKO Libraries and Full Customization for Any CRISPR Screening Experiment

    SANTA CLARA, Calif., Oct. 20, 2016

  • Agilent's DNA Integrity Number (DIN)

    Base your genomic DNA sample QC on science not personal interpretation

  • GeneSpring GX

    GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. Designed specifically for the needs of biologists, GeneSpring offers an interactive environment that promotes investigation and enables understanding of Transcriptomics, Genomics, Metabolomics and Proteomics data within a biological context.  NGS data can be aligned and analyzed in Strand NGS (Agilent’s business partner – free trial), and the imported reads, region and entities can be visualized in GeneSpring the Genome Browser, and further correlated with other data types. GeneSpring allows you to quickly and reliably identify targets of interest that are both statistically and biologically meaningful.

    • Statistical Analysis
    • Clustering and PCA
    • Multi-omic Analysis for Integrated Biology
    • Pathway Analysis and Visualizations
  • OneSeq: One Assay, All Variants

    Comprehensive Target Enrichment Panel for Genome-Wide Copy Number, LOH and Targeted Mutations - in ONE assay.

  • Streck Cell-Free DNA BCT®

    Blood Collection Tube for the preservation of cell-free DNA

  • Sureselect Human All Exon V7

    Sleek Design, Best-in-Class Coverage, Minimal Sequencing 

    The Agilent SureSelect Human All Exon V7 delivers unmatched coverage of targeted regions with minimal sequencing. Designed using the GRCh38/hg38 genome assembly, this exome design targets only coding regions from RefSeq, CCDS, GENCODE &USC Known Genes. all exon sequencing product features a novel bait design algorithm resulting in an end-to-end design size of only 48.2 MB. A novel bait design algorithm results in a sleek design with an end-to-end design size of only 48.2Mb.

    The exome sequencing system provides excellent uniformity and allows more samples to be pooled per flow cell, for more cost-effective sequencing. The accurate targeting ensures that even hard-to-capture exons can be accessed. In addition, the system is compatible with all SureSelect Library prep solutions, making it one of the most versatile exome solutions for a wide range of sample types including low input material and FFPE samples, and workflow needs such as enzymatic or mechanical shearing.