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Penghao Qian

dblp:340/3359 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2022
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 1, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › computational neuroscience
neuronal morphology
0.612022
Manifold classification of neuron types from microscopic images · Bioinform. 2022

Methods — techniques the papers use, named apart from their topics

minimum spanning tree · 0.6manifold classification · 0.6locally linear embedding · 0.6
YearPublicationVenuePosition
2022 Manifold classification of neuron types from microscopic images
abstract
Analysis of cell types is recognized as a major task in current single-cell genotyping and phenotyping. In neuroscience, 3-D neuron morphologies are often reconstructed from multi-dimensional microscopic images. Recent studies indicate that neurons could form very complicated distributions in the feature space, and thus they can be explored using manifold analysis. We have developed manifold classification toolkit software to replace the conventional clustering analysis to discover cell subtypes from three state-of-the-art collections of single neurons' 3-D morphologies that reconstructed from images. We have gathered 9208 3-D spatially registered whole mouse brain neurons from three datasets with the highest quality to date generated by the single neuron morphology community. To explore manifold distribution, our method uses minimum spanning tree-based principal skeletons to approximate locally linear embeddings, to explore the morphological feature spaces, which correspond to dendritic arbors, axonal arbors or both categories of arborization patterns of neurons. We show manifold classification is a suitable approach for a majority of often referred cell types, each of which was also discovered to contain multiple subtypes. Our results show an initial effort to employ manifold classification but not traditional clustering analysis as an alternative framework for analyzing 3-D neuron morphologies reconstructed from 3-D microscopic images. AVAILABILITY AND IMPLEMENTATION: Freely available at https://github.com/Mr-strlen/Cell_Pattern_Analysis_Tool.'
Penghao Qian
Bioinform.2