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Multiscale Topology of Chromatin Folding
Genomics · Submitted 4 Nov 2015
abstract compiled · 2026-09-23 · no language-model review
The authors' main claim We identify substantial multiscale topology in these datasets.
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The abstract, sentence by sentence
The three dimensional structure of DNA in the nucleus (chromatin) plays an important role in many cellular processes. Recent experimental advances have led to high-throughput methods of capturing information about chromatin conformation on genome-wide scales. New models are needed to quantitatively interpret this data at a global scale. Here we introduce the use of tools from topological data analysis to study chromatin conformation. We use persistent homology to identify and characterize conserved loops and voids in contact map data and identify scales of interaction. We demonstrate the utility of the approach on simulated data and then look data from both a bacterial genome and a human cell line. We identify substantial multiscale topology in these datasets.
background contribution method result interpretation main claim
| # | sentence | role | the authors' own work | states the main conclusion | strength |
|---|---|---|---|---|---|
| s0 | The three dimensional structure of DNA in the nucleus (chromatin) plays an important role in many cellular processes. | background 1.00 | 0.04 | 0.02 | asserted 1.00 |
| s1 | Recent experimental advances have led to high-throughput methods of capturing information about chromatin conformation on genome-wide scales. | background 1.00 | 0.05 | 0.02 | asserted 1.00 |
| s2 | New models are needed to quantitatively interpret this data at a global scale. | gap 0.97 | 0.05 | 0.03 | asserted 0.94 |
| s3 | Here we introduce the use of tools from topological data analysis to study chromatin conformation. | contribution 0.90 | 0.86 | 0.04 | asserted 0.94 |
| s4 | We use persistent homology to identify and characterize conserved loops and voids in contact map data and identify scales of interaction. | method 0.98 | 0.95 | 0.12 | asserted 1.00 |
| s5 | We demonstrate the utility of the approach on simulated data and then look data from both a bacterial genome and a human cell line. | method 0.64 | 0.94 | 0.05 | asserted 0.95 |
| s6 | We identify substantial multiscale topology in these datasets. | result 1.00 | 0.96 | 0.77 | asserted 1.00 |
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The paper
Original abstract
The three dimensional structure of DNA in the nucleus (chromatin) plays an important role in many cellular processes. Recent experimental advances have led to high-throughput methods of capturing information about chromatin conformation on genome-wide scales. New models are needed to quantitatively interpret this data at a global scale. Here we introduce the use of tools from topological data analysis to study chromatin conformation. We use persistent homology to identify and characterize conserved loops and voids in contact map data and identify scales of interaction. We demonstrate the utility of the approach on simulated data and then look data from both a bacterial genome and a human cell line. We identify substantial multiscale topology in these datasets.
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References
How the literature uses it
5 arXiv papers cite this in 13 sentences
Papers citing it · 8 sentences without a confident label
Uses its method or tool 1 paper
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To overcome the potential complications arising from the non-uniqueness of generators we develop two complementary approaches: matroid generators, which are efficiently computed using matroid theory [ref] , and minimal generators [ref] , which we tailor to sequential datasets.
Hypergraphs for multiscale cycles in structured data · Introduction · 0.89
Cites it as background 1 paper
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One could adapt hyperTDA to other choices of generators [ref] depending on the data and the end goal; clearly the fledgling area of research into, and construction of, topology generators has opened up new mathematical avenues for mathematical exploration; but already they are proving to be immensely useful in topological data analysis.
Hypergraphs for multiscale cycles in structured data · Discussion · 0.81
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