INVIEW™ HUMAN EXOME
Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol for low-input samples (≥ 10ng) Available under diagnostics standard (ISO17025) INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications. Exome enrichment with the latest Agilent SureSele…
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Highlights:
- Fastest exome sequencing, starting from one sample
- Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample)
- Special protocol for low-input samples (≥ 10ng)
- Available under diagnostics standard (ISO17025)
INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications.
Exome enrichment with the latest Agilent SureSelect chemistry and massively parallel sequencing of the coding regions is a versatile and economic tool for researchers who want to identify relevant disease-causing mutations. Customers have the option to complement their BioIT analysis with the established QIAGEN Ingenuity Variant Analysis software. INVIEW HUMAN EXOME EXPLORE is ideal for studies on germline mutaitons, whereas INVIEW HUMAN EXOME ADVANCE is perfectly suited to investigations of both germline and somatic mutations. INVIEW™ HUMAN EXOME is a highly standardised complete solution for clinical and medical researchers to help them answer important questions faster.
