Single-cell Multi-omics Sequencing and Analyses of Human Colorectal Cancer
Source: NCBI BioProject (ID PRJNA382695)
Source: NCBI BioProject (ID PRJNA382695)
0 0
Project name: Homo sapiens
Description: Although genomic instability, epigenetic abnormality, and gene expression dysregulation are hallmarks of colorectal cancer, these features have not been simultaneously analyzed at single-cell resolution. Using optimized single-cell multi-omics sequencing together with multi-regional sampling of the primary tumor, lymphatic and distant metastases, we provide insights beyond intratumoral heterogeneity. Genome-wide DNA methylation levels were relatively consistent within a single genetic sub-lineage. The genome-wide DNA demethylation patterns of cancer cells were consistent in all 10 sequenced patients. Our work demonstrates the feasibility of reconstructing genetic lineages, and tracing their epigenomic and transcriptomic dynamics with single-cell multi-omics sequencing.Overall design: Single cell RNA-seq and Bisulfite-seq on whole cells or by TrioSeq2.[scTrioSeq2Rna and scTrioSeq2Met Samples]Sample Title structure: Library_PatientID_SamplingPositions_CellIDSamplingPositions abbreviations:PT: Primary TumorLN: Lymph Node metastasisML: Liver MetastasisMP: Post-treatment Liver Metastasis
Data type: Other
Sample scope: Multiisolate
Relevance: Medical
Organization: Fuchou Tang, School of life sciences, Peking University
Literatures
- PMID: 30498128
Last updated: 2017-04-12