Evidence map›Paper›PMID 25515433›Full record

ArticleMedical image analysis2015

A novel method for identifying a graph-based representation of 3-D microvascular networks from fluorescence microscopy image stacks.

Sepideh Almasi, Xiaoyin Xu, Ayal Ben-Zvi, Baptiste Lacoste, Chenghua Gu, Eric L Miller

Open access · greenAbstract read
In one paragraph

Article in Medical image analysis, 2015. 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
1.7field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

6 authors at 3 institutions in 1 country.

Sepideh AlmasiDept. Electrical and Computer Engineering, Tufts University, Medford, MA, USA.
Xiaoyin XuDept. Radiology, Brigham and Women's Hospital, Boston, MA, USA.
Ayal Ben-ZviDept. Neurobiology, Harvard Medical School, Boston, MA, USA.
Baptiste LacosteDept. Neurobiology, Harvard Medical School, Boston, MA, USA.
Chenghua GuDept. Neurobiology, Harvard Medical School, Boston, MA, USA.
Eric L MillerDept. Electrical and Computer Engineering, Tufts University, Medford, MA, USA.
Harvard University · USTufts University · USBrigham and Women's Hospital · US

Funding

A novel informatics approach to understanding complex muscle fiber phenotypesR01LM011415 · NLM · BRIGHAM AND WOMEN'S HOSPITAL · PI XU, XIAOYIN · 2014 to 2017
$1.5M
NLM NIH HHS R01 LM011415
6 · The paper itself

Abstract

A novel approach to determine the global topological structure of a microvasculature network from noisy and low-resolution fluorescence microscopy data that does not require the detailed segmentation of the vessel structure is proposed here. The method is most appropriate for problems where the tortuosity of the network is relatively low and proceeds by directly computing a piecewise linear approximation to the vasculature skeleton through the construction of a graph in three dimensions whose edges represent the skeletal approximation and vertices are located at Critical Points (CPs) on the microvasculature. The CPs are defined as vessel junctions or locations of relatively large curvature along the centerline of a vessel. Our method consists of two phases. First, we provide a CP detection technique that, for junctions in particular, does not require any a priori geometric information such as direction or degree. Second, connectivity between detected nodes is determined via the solution of a Binary Integer Program (BIP) whose variables determine whether a potential edge between nodes is or is not included in the final graph. The utility function in this problem reflects both intensity-based and structural information along the path connecting the two nodes. Qualitative and quantitative results confirm the usefulness and accuracy of this method. This approach provides a mean of correctly capturing the connectivity patterns in vessels that are missed by more traditional segmentation and binarization schemes because of imperfections in the images which manifest as dim or broken vessels.

Indexed as

AnimalsDatasets as TopicImaging, Three-DimensionalMicroscopy, FluorescenceMicrovesselsModels, CardiovascularSensitivity and SpecificityConvex hullGraph extractionJunction detectionMicrovascular networkTubular structures

Identifiers

PMID25515433
PMCPMC4955560
OpenAlexW2045428587

What OpenQuestion holds

Textmetadata
LicenceTDM
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.