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NGS exome panels offer the depth and breadth of coverage you need for discovering mutations associated with diseases.
Agilent cancer NGS assays and panels detect content relevant in oncology, including somatic cancer SNVs, indels, CNVs and translocations.
Agilent NGS Custom Target Enrichment probes can be utilized to design customized hybrid capture panels to target any coding or non-coding regions of the genome or the transcriptome.
Agilent offers NGS designs for comprehensive or focused coverage of genes relevant to human genetics research.
Agilent offers NGS designs targeting genomic regions for epigenetics research.
NGS panels targeting pathogens for infectious disease research
Agilent offers NGS targeted DNA sequencing panels for plant genotyping and genetic research in model organisms that are both comprehensive and cost-effective.
NGS Quality Control for library preparation and experiments is important for achieving accurate, and reliable results.
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The SureSelect Clinical Research Exome, in addition to providing deeper coverage of the most relevant disease-associated targets, is the only exome on the market to come with a list of included genes and their evidence for disease relevance.
Confident results & efficient sequencing powered by V8’s comprehensive content & great performance.
SureSelect Focused Exome captures more disease-associated regions for more comprehensive analysis.
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