Evidence map›Paper›PMID 26141505›Full record

ArticleBMC bioinformatics2015

Topological characterization of neuronal arbor morphology via sequence representation: II--global alignment.

Todd A Gillette, Parsa Hosseini, Giorgio A Ascoli

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2015. 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
5.8field-weighted citation impact, top 5% 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, 33 citations in OpenAlex.

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  8. Objective Morphological Classification of Neocortical Pyramidal Cells.Cerebral cortex (New York, N.Y. : 1991) · 2019
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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 at 2 institutions in 1 country.

Todd A GilletteDepartment of Molecular Neuroscience, Center for Neural Informatics, Structures, and Plasticity, Krasnow Institute for Advanced Study (MS2A1), George Mason University, Fairfax, VA, USA. todd.gillette@gmail.com.
Parsa HosseiniDepartment of Molecular Neuroscience, Center for Neural Informatics, Structures, and Plasticity, Krasnow Institute for Advanced Study (MS2A1), George Mason University, Fairfax, VA, USA. phosseini13@gmail.com.
Giorgio A AscoliDepartment of Molecular Neuroscience, Center for Neural Informatics, Structures, and Plasticity, Krasnow Institute for Advanced Study (MS2A1), George Mason University, Fairfax, VA, USA. ascoli@gmu.edu.
Institute for Advanced Study · USGeorge Mason University · US

Funding

Generation and Description of Neuronal Morphology and ConnectivityR01NS039600 · NINDS · GEORGE MASON UNIVERSITY · PI ASCOLI, GIORGIO A · 1999 to 2024
$6.9M
Cytoskeletal mechanisms of dendrite arbor shape developmentR01NS086082 · NINDS · GEORGIA STATE UNIVERSITY · PI ASCOLI, GIORGIO A, COX, DANIEL N · 2013 to 2023
$3.1M
NINDS NIH HHS R01 NS039600NINDS NIH HHS R01 NS086082NINDS NIH HHS R01 NS39600
6 · The paper itself

Abstract

backgroundThe increasing abundance of neuromorphological data provides both the opportunity and the challenge to compare massive numbers of neurons from a wide diversity of sources efficiently and effectively. We implemented a modified global alignment algorithm representing axonal and dendritic bifurcations as strings of characters. Sequence alignment quantifies neuronal similarity by identifying branch-level correspondences between trees.

resultsThe space generated from pairwise similarities is capable of classifying neuronal arbor types as well as, or better than, traditional topological metrics. Unsupervised cluster analysis produces groups that significantly correspond with known cell classes for axons, dendrites, and pyramidal apical dendrites. Furthermore, the distinguishing consensus topology generated by multiple sequence alignment of a group of neurons reveals their shared branching blueprint. Interestingly, the axons of dendritic-targeting interneurons in the rodent cortex associates with pyramidal axons but apart from the (more topologically symmetric) axons of perisomatic-targeting interneurons.

conclusionsGlobal pairwise and multiple sequence alignment of neurite topologies enables detailed comparison of neurites and identification of conserved topological features in alignment-defined clusters. The methods presented also provide a framework for incorporation of additional branch-level morphological features. Moreover, comparison of multiple alignment with motif analysis shows that the two techniques provide complementary information respectively revealing global and local features.

Indexed as

AlgorithmsAnimalsAxonsBase SequenceDendritesDrosophilaMiceMolecular Sequence DataNeuronsPhylogenySequence Homology, Nucleic Acid

Identifiers

PMID26141505
PMCPMC4491275
OpenAlexW2106091890

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.