80 results found for "Somatic variants"
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consumable
Advanta Assays and Kits
Combining microfluidics technology with optimized reagents produces high-quality results in less time. …
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Infographic
The Search for the Hidden Mutation, One Cell at a Time
This Fluidigm infographic shows how somatic mutations cause disease, including how single-cell DNA sequencing can reveal hidden mutations in cell populations.
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media
To Cure Cancer, Identify Every Cell
Discover hidden clonalities through single-cell DNA seq with this visual infographic …
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brochure
Advanta Solid Tumor NGS Library Prep Assay
To advance our understanding of cancer and make strides toward improved patient care, researchers have a growing need to interrogate somatic mutations, often from limited quantities of available samples.
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article
Advanta Solid Tumor NGS Library Prep Assay
Confidently analyze multiple somatic variants with a flexible, automated NGS workflow …
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brochure
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article
Advanta Oncology Assays
The variants you need. The workflow you'll love. …
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Release notes
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Publications
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Poster
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article
Advanta RNA Fusions NGS Library Prep Assay
Analyze over 380 gene fusion pairs with a flexible, automated NGS workflow …
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technical note
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technical note
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technical note
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media
Tie a Pink Ribbon on Breast Cancer Treatment
Single-cell exome sequencing reveals cell population insights for better therapies …
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consumable
Targeted DNA Seq
Achieve economy of scale with ease …
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Protocol
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faq
Can I add other variants of interest that are not covered by the Advanta CFTR NGS Library Prep Assay?
Yes. Assays designed for other variants, including those within other genes, may be added to the open assay inlets of the integrated fluidic circuit (IFC). …
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faq
Which CFTR variants does the Advanta CFTR NGS Library Prep Assay cover and how were they chosen?
The Advanta™ CFTR NGS Library Prep Assay was designed to support the sequencing of all 27 exons of the CFTR gene along with select intronic regions. …
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Protocol
C1 System for DNA Sequencing Protocol
version I1