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4dn:methods [2024/01/16 09:56] rcalandrelli created |
4dn:methods [2025/04/22 16:21] (current) |
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| - | ====== 4DN-created methods to search in full scope analysis ====== | + | ====== 4DN Methods ====== |
| - | * C-BERST | + | [[https://docs.google.com/spreadsheets/d/1z89XhSBqEyHvXvy6QRDzruR43E6jHvW-1sa8yEcd0wY/edit?usp=sharing|Here is a list]] of the 4DN-created methods to search in full scope analysis to identify how used they are across publications. |
| - | * ChIA-Drop | + | Please let us know if your method is missing. |
| - | + | ||
| - | * ChIA-PET | + | |
| - | + | ||
| - | * Chromatin interaction analysis by paired-end tag sequencing | + | |
| - | + | ||
| - | * Chromatin interaction analysis in droplet | + | |
| - | + | ||
| - | * COLA | + | |
| - | + | ||
| - | * concatemer ligation assay | + | |
| - | + | ||
| - | * DamID seq | + | |
| - | + | ||
| - | * DNA multiplexed error-robust fluorescence in situ hybridization | + | |
| - | + | ||
| - | * DNA-MERFISH | + | |
| - | + | ||
| - | * DNase Hi-C | + | |
| - | + | ||
| - | * DNAseqFISH | + | |
| - | + | ||
| - | * E/L Repli-seq | + | |
| - | + | ||
| - | * FISH omics | + | |
| - | + | ||
| - | * Genome architecture mapping | + | |
| - | + | ||
| - | * GPSeq | + | |
| - | + | ||
| - | * Hi-C 3.0 (not “Hi-C” alone) | + | |
| - | + | ||
| - | * Hi-M | + | |
| - | + | ||
| - | * iMARGI | + | |
| - | + | ||
| - | * in situ ChIA-PET | + | |
| - | + | ||
| - | * in situ genomic sequencing | + | |
| - | + | ||
| - | * in situ Hi-C | + | |
| - | + | ||
| - | * in situ mapping of RNA-genome interactions | + | |
| - | + | ||
| - | * integrative genome modeling platform | + | |
| - | + | ||
| - | * LC-HI-C | + | |
| - | + | ||
| - | * Liquid chromatin Hi-C | + | |
| - | + | ||
| - | * Local proteome of specific genomic loci | + | |
| - | + | ||
| - | * MC-3C | + | |
| - | + | ||
| - | * Micro-C | + | |
| - | + | ||
| - | * MINA | + | |
| - | + | ||
| - | * Multi-contact 3C | + | |
| - | + | ||
| - | * multiplexed FISH | + | |
| - | + | ||
| - | * multiplexed imaging of nucleome architecture | + | |
| - | + | ||
| - | * OligoDNA-PAINT | + | |
| - | + | ||
| - | * OligoFISSEQ | + | |
| - | + | ||
| - | * Oligopaint fluorescent in situ sequencing | + | |
| - | + | ||
| - | * Oligopaints | + | |
| - | + | ||
| - | * OligoSTORM | + | |
| - | + | ||
| - | * Optical reconstruction of chromatin architecture | + | |
| - | + | ||
| - | * ORCA | + | |
| - | + | ||
| - | * PLAC-seq | + | |
| - | + | ||
| - | * Proximity-ligation assisted ChIP-seq | + | |
| - | + | ||
| - | * Repli-seq | + | |
| - | + | ||
| - | * sci-Hi-C | + | |
| - | + | ||
| - | * sci-RNA-seq | + | |
| - | + | ||
| - | * sci-TIP | + | |
| - | + | ||
| - | * seqFISH | + | |
| - | + | ||
| - | * Split-pool recognition of interactions by tagextension | + | |
| - | + | ||
| - | * SPRITE | + | |
| - | + | ||
| - | * Time-resolved DamID | + | |
| - | + | ||
| - | * TSA sequencing | + | |
| - | + | ||
| - | * TSA-seq | + | |