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Updated: May 18, 2026

An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues
Published on: April 5, 2018
What are we learning from the cancer genome?
Eric A Collisson1, Raymond J Cho, Joe W Gray
1Department of Medicine/Hematology and Oncology, University of California San Francisco, 505 Parnassus Avenue, San Francisco, CA 94143, USA.
Massively parallel sequencing reveals significant genetic heterogeneity in human cancers. Overcoming challenges in genomic analysis is key to advancing precision cancer medicine in clinical practice.
Area of Science:
- Genomics
- Oncology
- Bioinformatics
Background:
- Next-generation sequencing (NGS) technologies have rapidly advanced, becoming accessible and affordable.
- NGS has profoundly impacted the study of human cancer, revealing new genomic features.
Purpose of the Study:
- To review insights from large-scale genomic profiling of cancer.
- To focus on findings with potential to influence future clinical practice.
Main Methods:
- Review of recent advancements in massively parallel sequencing.
- Analysis of large-scale cancer genome data.
Main Results:
- Identification of substantial genetic heterogeneity within cancer types using high-resolution profiling and large sample sets.
- Challenges in distinguishing driver mutations from background somatic events in cancer genomes.
Conclusions:
- Genomic profiling offers valuable insights into cancer but faces challenges in clinical implementation.
- Organizational, regulatory, and societal hurdles must be addressed for precision cancer medicine to become standard care.
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