Reduce turn-around times with streamlined NGS Panels

SEE THE PANELS

Simple, robust and precise NGS enrichment for any target

We understand your pain points

  • Insufficient starting material
  • Labor costs
  • Uneven coverage
  • Costly reruns
  • Unique targets

So we built a simpler solution

Targeted panels that run on SLIMamp for single-tube, single-day library preps with minimal, flexible inputs and uniform coverage. 

Supported by the PiVAT bioinformatics platform for robust enrichment for variant detection at down to 1% allele frequency or <1% for PillarHS (high sensitivity) panels.

Enhanced sensitivity with PillarHS

PillarHS panels incorporate unique molecular IDs (UIDs, also called UMIs) for enhanced sensitivity. PillarHS panels are ideal for early detection or identifying minimally residual disease and are specifically designed for use with cell-free DNA.

Learn more about PillarHS

Panels available for Illumina, MGI, and Thermo sequencers

View poster from ESHG 2020

Solid Tumor Panels

Targets include multi-cancer, breast, lung, and colon. Includes panels specialized to detect fusions and CNVs.

Blood Cancer Panels

Targets include myeloid cancers and myeloprolifitive neoplasm.

Inherited Disease Panels

Targets include cystic fibrosis, thalassemia, and BRCA1/BRCA2.

Custom Panels

Design your own custom panel with a one-day workflow via the ampPD™ primer design platform.

Find a panel that suits your targets or design your own

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Pillar Biosciences, Inc.
9 Strathmore Rd
Natick, MA 01760

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© 2020 Pillar Biosciences
For research use only. Not for use in diagnostic procedures.
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