Single-cell and spatial Hi-C¶
Single-cell Hi-C (and Dip-C, scMicro-C, sci-Hi-C) gives each cell a sparse list of contacts — pairs of loci that were close in that nucleus; the multi-omics variants add the cell’s transcriptome or accessibility (HiRES, GAGE-seq, scHiCAR, Paired / Droplet Hi-C), and spatial Hi-C measures contacts per spot of a tissue section. Contacts are not coordinates: U-Chrom keeps them as contact maps linked to the cells, and computes coordinates from them when you want structures.
Step |
API |
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read contacts: |
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link per-cell contact maps ( |
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link RNA / ATAC matrices ( |
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3-D structures of one cell, an ensemble of models (native engine, CPU or GPU) |
EMber: |
contacts of a structure (to compare with the input) |
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cell features from contact maps; Higashi / FastHigashi |
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spots of a section in the tissue |
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The atlas holds single-cell and spatial Hi-C datasets ready to open — HiRES, dscHi-C, GAGE-seq, Droplet and Paired Hi-C, scHiCAR, Uni-C, Stevens 2017 with its published structures, spatial Hi-C, spatial ATAC-Hi-C and Hi-C-RNA sections (datasets).
Tutorials¶
The scHiCAR part of cell embeddings embeds the same cells by their contact maps, their RNA and their accessibility.
Guides¶
Then¶
Reconstructed models are coordinates like traced ones: distance maps and contact frequencies of the models (per-locus features), comparisons with imaging of the same cell type, and the web browser, which shows each cell’s models next to its own contact map. Linked contact maps, pseudo-bulk maps per cell type and embedded copies for sharing: data model & storage.
API: uchrom.recon, uchrom.emb, uchrom.io.