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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.

how it is stated · asserted 1.00 read the record →

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arXiv ID1511.01426 (version 1)
Pith ID6Y7KRPWJ, Pith's permanent record of this paper and its review
CitationBenjamin Schweinhart, Kevin Emmett, Raul Rabadan. "Multiscale Topology of Chromatin Folding." arXiv:1511.01426 (2015). https://pith.science/paper/6Y7KRPWJ
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Compiled by classifier-1.13.0 via TypeSafe API, question bank abstract-p1-20260923, 2026-09-23: 1 request, 5,398 input tokens.

What the abstract itself states, as probabilities: claims first 0.06 · states limitation 0.06 · human participants 0.14 · controlled comparison 0.05 · randomized assignment 0.01 · states quantitative result 0.05 · compares with prior results 0.10 · mentions code or data availability 0.03.

The abstract, sentence by sentence

arXiv listing abstract v1. Results and the main claim are underlined; .

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

What the classifier reports for each sentence. The number is the probability it gave the label.
#sentencerolethe authors' own workstates the main conclusionstrength
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

What kind of paper the classifier reports this is: method or tool 1.00 · evidence from analysis of existing data 0.93.

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Every quoted sentence on this record is the authors'. Every label is from Pith's closed vocabulary, with the probability shown beside it. Every number in the measurements table is the authors', checked by code. Record as JSON

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

Each citing sentence is taken from the citing paper's LaTeX source and typed by Pith's classifier. A label appears at probability 0.8 or more (0.95 for support), a contest at 0.7 or more; the quoted words are the citing authors'. How each label was checked · JSON

Papers citing it · 8 sentences without a confident label

Uses its method or tool 1 paper
  • 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
  • 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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