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Automated analysis of whole brain vasculature using machine learning

Automated analysis of whole brain vasculature using machine learning

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2211214108

Automated analysis of whole brain vasculature using machine learning

About this item

Full title

Automated analysis of whole brain vasculature using machine learning

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2019-04

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Tissue clearing methods enable imaging of intact biological specimens without sectioning. However, reliable and scalable analysis of such large imaging data in 3D remains a challenge. Towards this goal, we developed a deep learning-based framework to quantify and analyze the brain vasculature, named Vessel Segmentation & Analysis Pipeline (VesSAP). Our pipeline uses a fully convolutional network with a transfer learning approach for segmentation. We systematically analyzed vascular features of the whole brains including their length, bifurcation points and radius at the micrometer scale by registering them to the Allen mouse brain atlas. We reported the first evidence of secondary intracranial collateral vascularization in CD1-Elite mice and found reduced vascularization in the brainstem as compared to the cerebrum. VesSAP thus enables unbiased and scalable quantifications for the angioarchitecture of the cleared intact mouse brain and yields new biological insights related to the vascular brain function. Footnotes * http://DISCOtechnologies.org/VesSAP...

Alternative Titles

Full title

Automated analysis of whole brain vasculature using machine learning

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2211214108

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2211214108

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/613257