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NGS and Proteomics Data Analysis

Clear results from complex omics data sets

We are experts in the correct application of standard and custom OMICs data processing pipelines. Many platforms offer standard next-generation sequence analysis for RNASeq and DNASeq, but none help a new organization correctly understand and interpret those results. Boulder BioConsulting staff have over 50 years of experience with complex OMICs data analysis and bring the experience and scientific acumen necessary to derive reliable insights from these high-dimensional, challenging scientific data types. This experience can help you with:

  • RNASeq analysis
  • DNASeq analysis, variant calling and interpretation
  • ChIPSeq analysis
  • Custom pipeline development for your unique application and science
  • Multi-omics integrated data analysis

Most recently, we have focused on Proteomics analysis as a raising field and can offer unique experience with interpreting the results from platforms like:

In addition, we have a leading expert in the development of multiplexed molecular diagnostic experiment design. Correct multiplexing, sequencing, amplification, and identification strategies are critical for enabling high-throughput and accurate data, which all derive from rigorous and intelligent primer design. BBC has a leading expert who has been responsible for whole Affymetrix chip designs and whose algorithmic insights have enabled several successful products to be brought to market. This experience can help you with:

  • CRISPR guide RNA.
  • Multiplex nucleic acid detection.
  • Complex, atypical sequence analysis problems.
  • Molecular diagnostic panels.

Expertise in

Trusted by industry leaders

Sagimet Biosciences
NYU Tisch School of the Arts
University of Colorado
Mayo Clinic
Think Bioscience
G3 Pharmaceuticals
Clene Nanomedicine

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