Literature request

Please complete the form below to request electronic copies of selected literature.

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Selected literature for research

Late-breaking material

Brochure: Targeted Sequencing Solutions for Oncology Research

White paper: An approach for establishing Oncomine Focus Assay performance

Selected assays and panels

NEW Ion Torrent™ Oncomine™ BRCA Research Assay

NEW Ion AmpliSeq™ Direct FFPE DNA Kit

Ion Torrent™ Oncomine™ Comprehensive Assay

Ion Torrent™ Oncomine™ cfDNA Assays

Ion Torrent™ Oncomine™ Focus Assay

Ion AmpliSeq™ DNA Custom Panels

Ion AmpliSeq™ Cancer Hotspot Panel v2

Ion AmpliSeq™ Infectious Disease Panels

Ion AmpliSeq™ Inherited Disease Panels

Ion AmpliSeq™ Transcriptome Kit

Ion 16S™ Metagenomics Kits

Applied Biosystems™ TaqMan® Advanced miRNA Assays

Applied Biosystems™ TaqMan® Gene Expression Assays

Applied Biosystems™ TaqMan® Genotyping Assays

TaqMan® Assays for Women's Health Research

Ion AmpliSeq™ and TaqMan® Assays for Pharmacogenomics Research

Informatics

Ion Torrent™ Oncomine™ NGS Informatics

Ion Reporter™ Software & Server

Minor Variant Finder Software for Sanger Sequencing

Instruments

Ion S5™ System

Ion PGM™ System

Ion Chef™ System

Ion Torrent™ LiquidBiopsy™ Platform

Applied Biosystems™ Arcturus™ Laser Capture Microdissection System

Applied Biosystems™ QuantStudio™ 3/5 Real-Time PCR System

Applied Biosystems™ QuantStudio™ 3D Digital PCR System

Applied Biosystems™ 3500 Genetic Analyzer

Reagents and consumables

Applied Biosystems™ TaqPath™ qPCR Master Mix

DNA Purification

Applied Biosystems™ TaqMan® Fast Advanced Master Mix

Scientific posters

Multiplex TaqMan Assays for rare mutation analysis for using digltal PCR

Automated, purification-free, Ion AmpliSeq library preparation from FFPE samples using the Ion Chef System

Detection of somatic mutations at 0.1% frequency from cfDNA in peripheral blood with a multiplex next-generation sequencing assay

Minor Variant Finder: new software for detecting somatic mutations at low levels in Sanger sequencing traces

A next-generation sequencing-based sample-to-result pharmacogenomics research solution enables both SNV and CNV detection at once

Novel biomarkers and multiplexed NGS to stratify FFPE NSCLC by tumor-infiltrating lymphocytes and histopathology phenotypes

Clinical research results for an NGS-based kit for targeted detection of relevant gene rearrangements in lung tumor samples

Gene fusion database to create custom panels: enabling detection of fusion transcripts and gene expression assays

Application notes

Using Sanger CE to confirm variants discovered by NGS

Low-level somatic variant detection in tumor FFPE samples by Sanger sequencing

A simplified DNA extraction method for Sanger sequencing of FFPE samples

Sanger sequencing using Ion AmpliSeq primers and libraries

Next-generation sequencing analysis of low-frequency mutations from cell-free DNA

Using the versatile Ion S5 System for cancer genomics and transcriptomics research

Mutational analysis of cfDNA, CTC and germline DNA from a single blood sample

A complete next-generation sequencing workflow for circulating cell-free DNA isolation and analysis

For Research Use Only. Not for use in diagnostic procedures.

Selected literature for in vitro diagnostic use kits and instruments

Ion PGM™ Dx System

Applied Biosystems™ Veriti™ Dx System

Applied Biosystems™ QuantStudio™ Dx Real-Time PCR System

Applied Biosystems™ 7500 Fast Dx Real-Time PCR Instrument

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All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified. TaqMan is a registered trademark of Roche Molecular Systems, Inc., used under permission and license. LiquidBiopsy is a trademark of Cynvenio Biosystems, Inc.