Evidence map›Paper›PMID 32009153›Full record

ArticleNucleic acids research2020

BHi-Cect: a top-down algorithm for identifying the multi-scale hierarchical structure of chromosomes.

Vipin Kumar, Simon Leclerc, Yuichi Taniguchi

Abstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Vipin KumarLaboratory for Cell Systems Control, RIKEN Center for Biosystems Dynamics Research, Suita, Osaka 5650874, Japan.
Simon LeclercLaboratory for Cell Systems Control, RIKEN Center for Biosystems Dynamics Research, Suita, Osaka 5650874, Japan.
Yuichi TaniguchiLaboratory for Cell Systems Control, RIKEN Center for Biosystems Dynamics Research, Suita, Osaka 5650874, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput chromosome conformation capture (Hi-C) technology enables the investigation of genome-wide interactions among chromosome loci. Current algorithms focus on topologically associating domains (TADs), that are contiguous clusters along the genome coordinate, to describe the hierarchical structure of chromosomes. However, high resolution Hi-C displays a variety of interaction patterns beyond what current TAD detection methods can capture. Here, we present BHi-Cect, a novel top-down algorithm that finds clusters by considering every locus with no assumption of genomic contiguity using spectral clustering. Our results reveal that the hierarchical structure of chromosome is organized as 'enclaves', which are complex interwoven clusters at both local and global scales. We show that the nesting of local clusters within global clusters characterizing enclaves, is associated with the epigenomic activity found on the underlying DNA. Furthermore, we show that the hierarchical nesting that links different enclaves integrates their respective function. BHi-Cect provides means to uncover the general principles guiding chromatin architecture.

Indexed as

AlgorithmsCell LineChromatin Assembly and DisassemblyChromosome MappingChromosomes, HumanDNAFibroblastsGenetic LociHumansMultigene FamilyDNA

Identifiers

PMID32009153
PMCPMC7049727

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.