A complete service offering for error corrected sequencing.

Increase sensitivity of your NGS experiment 100X to discover what you’ve never been able to measure

Separate the Signal from the Noise

The standard NGS process introduces errors during PCR and the sequencing workflow. These errors result in noise that makes it challenging to differentiate between errors and true variants.

RareSeq™ eliminates the noise

How it Works

We use a proprietary unique molecular index strategy combined with a custom bioinformatics pipeline to identify ultra-rare variants- down to 1:10,000

Sequencing errors are corrected by aligning reads sharing the same UMI

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Ultra-sensitive and Quantitative

Detect and quantitate previously undetectable mutations in heterogeneous DNA with RareSeq™. Quantitative to a variant allele frequency (VAF) of 1:10,000, RareSeq™ is a highly reproducible and sensitive to identify indels and SNVs.

Accuracy and Precision

The error rate of NGS has been reported to be between 1-3%. Ensuring variant detection is accurate, RareSeq™ is validated by ddPCR demonstrating the high degree of correlation in identified variant allele fractions (VAFs).


TruSight® Myeloid Panel covers 54 genes found to be mutated in hematologic malignancies.


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TruSight® is a registered trademark of Illumina, Inc. and is used without permission. No challenge to the rights of Illumina is intended or implied.


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