Prognostic whole-genome and transcriptome signatures in colorectal cancers
Colorectal cancer (CRC) is caused by a sequence of somatic genomic alterations affecting driver genes in core cancer pathways1. To understand the functional and prognostic impact of cancer-causing somatic mutations, we analysed the whole genomes and transcriptomes of 1,063 primary CRCs in a population-based cohort with long-term follow-up. This study constitutes the largest integrated genome and transcriptome analysis of CRC to date, and links mutations, gene expressions and patient outcomes.
- Type: Transcriptome Sequencing
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
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EGAD50000000169 | BGISEQ-500 | 1183 |
Publications | Citations |
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Prognostic genome and transcriptome signatures in colorectal cancers.
Nature 633: 2024 137-146 |
4 |