Genomic testing for multiple myeloma, colorectal, and bile-duct cancers

Genome Characterization Unit

NIH-funded research Washington University · NIH-11191583

Comprehensive CLIA-certified genomic testing of tumor, normal tissue, and blood for people with multiple myeloma, colorectal cancer, or cholangiocarcinoma to identify mutations and support care decisions.

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionWashington University NIH-funded
Lab location1 site (Saint Louis, United States)
Project IDNIH-11191583 on NIH RePORTER

What this research studies

If you participate, your diagnostic tumor tissue, matched normal tissue, and sometimes blood will be processed under CLIA-compliant procedures for high-quality genetic testing. The program performs deep tumor/normal whole-exome sequencing (~250X), tumor-only whole-genome sequencing (~60X), RNA sequencing, and very deep targeted sequencing (>10,000X) of tumor DNA or cell-free DNA using unique molecular indexes to sensitively detect mutations. Selected samples may also undergo single-cell RNA sequencing, proteomics, and cellular imaging to improve understanding of tumor biology. Testing and planned follow-up collections occur year-by-year within the Washington University PE-CGS program with integrated quality management.

Who could benefit from this research

Good fit: People with a diagnosis of multiple myeloma, colorectal cancer, or cholangiocarcinoma who can provide diagnostic tumor tissue and matched normal samples (and sometimes blood) through the Washington University PE-CGS program.

Not a fit: People without these cancer types, those unable to provide suitable tissue or blood samples, or whose tumors lack clinically actionable mutations may not gain direct benefit.

Why it matters

Potential benefit: Could reveal actionable mutations to help match patients with targeted therapies and enable very sensitive monitoring of tumor mutations over time.

How similar studies have performed: High-depth exome and targeted deep sequencing approaches with UMIs have been successfully used in cancer diagnosis and monitoring, while the integrated use of WES, WGS, RNA-seq and single-cell/proteomic assays is more advanced and partly novel.

Where this research is happening

Saint Louis, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.