FFPE sequencing and arrays

Solutions designed to meet the challenges of analyzing degraded or limited genomic material

FFPE Sample Analysis

Specifically designed to meet the challenges of utilizing formalin-fixed, paraffin-embedded (FFPE) samples for genetic analyses, the Illumina portfolio of FFPE solutions provides a comprehensive range of FFPE sequencing and microarray applications. These solutions leverage optimized workflows and technologies for FFPE samples, which generally contain partially degraded or limited genomic material. Researchers can now analyze previously inaccessible samples to derive high quality genomic data and insight. With seamless solutions that encompass innovative preparation methods, leading next-generation sequencing and array platforms, and intuitive data analysis tools, FFPE sequencing and array studies have never been easier.

New QC Method for FFPE Sequencing

A novel QC approach enables researchers to sequence degraded DNA from FFPE tumor samples successfully.

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Targeted sequencing focuses on a select set of genes or gene regions that are chosen based on a priori knowledge. By sequencing targeted DNA regions, researchers can perform cost-effective, high-depth sequencing with a more streamlined data analysis pipeline.

To facilitate targeted cancer FFPE sequencing studies, Illumina offers fixed panels for guaranteed performance, and a custom amplicon solution where researchers can choose their amplicons of interest.

TruSight Tumor 170 is a comprehensive panel that detects single-nucleotide variants (SNVs), amplifications, and indels that contribute to solid tumor progression from 40 ng of nucleic acid, and is compatible with low-quality FFPE samples.

TruSight Tumor 15 enables molecular profiling of solid tumor specimens from FFPE tissue samples, delivering a high level of sensitivity for minor allele detection.

AmpliSeq for Illumina Cancer HotSpot Panel v2: Targeted research panel for investigating hotspot regions of 50 genes with known associations to cancer.

AmpliSeq for Illumina Comprehensive Cancer Panel: Targeted research panel for investigating the exonic regions of 409 genes with known associations to cancer.

FFPE Sample QC Recommendations

Extraction methods for FFPE tissue generally yield highly degraded DNA and RNA. Read our FFPE quality control recommendations to determine whether your FFPE samples are viable input material for Illumina library preparation kits.

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FFPE Sample QC Recommendations

Accurately measure gene expression at the transcript level and discover or validate gene fusions with our portfolio of RNA sequencing (RNA-Seq) library prep kits for FFPE sequencing.

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Sequencing FFPE Tumor Samples

See how Yasser Riazalhosseini, PhD sequences challenging FFPE cancer samples to identify driver genes and novel biomarkers.

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The TruSight RNA Pan-Cancer Panel enables comprehensive detection of 1385 gene fusions and gene expression changes, providing researchers with a focused view of the functionally relevant changes occurring in cancer. The panel is compatible with FFPE tissue and accommodates as little as 20 ng of total RNA input from FFPE. The TruSight RNA Pan-Cancer Panel provides a sensitive, reproducible, and economical solution for studies of expression dynamics and functional mechanisms in cancer.

TruSight Tumor 170 is a comprehensive panel that detects fusions and splice varients (as well as other variant classes) that contribute to solid tumor progression from 40 ng of nucleic acid and is compatible with low-quality FFPE samples.

TruSeq RNA Access Library Prep focuses your sequencing power on high-value coding RNA, making the most effective use of your read budget and enabling excellent data quality from as little as 20 ng of input RNA.

TruSeq Stranded Total RNA offers the most complete view of the transcriptome, capturing coding and non-coding RNA, while eliminating highly abundant RNA species such as ribosomal RNA.

TruSeq Targeted RNA Expression is an accurate and economical method for measuring dozens to thousands of RNA targets simultaneously, making it ideal for validating gene expression arrays and RNA-Seq studies.

Employing a streamlined workflow, all Illumina custom, semi-custom, and commercially available arrays can be used to genotype FFPE samples. This workflow utilizes the Infinium FFPE DNA Restoration Solution, which simplifies upfront sample processing by identifying samples of sufficient quality and repairing the damaged DNA in the samples for downstream genotyping.

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Methylation arrays enable quantitative interrogation of selected methylation sites across the genome at single-nucleotide resolution. Illumina methylation arrays provide a unique combination of comprehensive, expert-selected coverage, FFPE sample compatibility, high sample throughput, and an affordable price.

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