Evidence map›Paper›PMID 27036078›Full record

ArticleBMC genomics2016

A streamlined tethered chromosome conformation capture protocol.

Idan Gabdank, Sreejith Ramakrishnan, Anne M Villeneuve, Andrew Z Fire

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.9field-weighted citation impact, top 4% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Idan GabdankDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Sreejith RamakrishnanDepartments of Developmental Biology and Genetics, Stanford University School of Medicine, Stanford, California, 94304, USA.
Anne M VilleneuveDepartments of Developmental Biology and Genetics, Stanford University School of Medicine, Stanford, California, 94304, USA.
Andrew Z FireDepartments of Pathology and Genetics, Stanford University School of Medicine, Stanford, California, 94304, USA. afire@stanford.edu.
Stanford University · US

Funding

GENE REGULATION DURING EARLY DEVELOPMENT OF C. ELEGANSR01GM037706 · NIGMS · STANFORD UNIVERSITY · PI FIRE, ANDREW Z. · 1987 to 2018
$11.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
MEIOTIC CHROMOSOME SEGREGATION IN C. ELEGANSR01GM053804 · NIGMS · STANFORD UNIVERSITY · PI VILLENEUVE, ANNE M · 1996 to 2017
$5.7M
NIGMS NIH HHS R01 GM037706NIGMS NIH HHS R01 GM053804NIGMS NIH HHS R01GM37706NIGMS NIH HHS R01GM53804NIH HHS P40 OD010440
6 · The paper itself

Abstract

backgroundIdentification of locus-locus contacts at the chromatin level provides a valuable foundation for understanding of nuclear architecture and function and a valuable tool for inferring long-range linkage relationships. As one approach to this, chromatin conformation capture-based techniques allow creation of genome spatial organization maps. While such approaches have been available for some time, methodological advances will be of considerable use in minimizing both time and input material required for successful application.

resultsHere we report a modified tethered conformation capture protocol that utilizes a series of rapid and efficient molecular manipulations. We applied the method to Caenorhabditis elegans, obtaining chromatin interaction maps that provide a sequence-anchored delineation of salient aspects of Caenorhabditis elegans chromosome structure, demonstrating a high level of consistency in overall chromosome organization between biological samples collected under different conditions. In addition to the application of the method to defining nuclear architecture, we found the resulting chromatin interaction maps to be of sufficient resolution and sensitivity to enable detection of large-scale structural variants such as inversions or translocations.

conclusionOur streamlined protocol provides an accelerated, robust, and broadly applicable means of generating chromatin spatial organization maps and detecting genome rearrangements without a need for cellular or chromatin fractionation.

Indexed as

AnimalsCaenorhabditis elegansChromatinChromosome MappingChromosomesChromatinCaenorhabditis elegansChromatinConformationGenomeHi-CTCC

Identifiers

PMID27036078
PMCPMC4818521
OpenAlexW2331152091

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.