Healpix Pixelation

HEALPix pixelation is a method for dividing a spherical surface into equal-area, hierarchically organized pixels, enabling consistent storage and analysis of data distributed across directions or locations. It represents the sphere through twelve base-resolution cells that are recursively subdivided, while preserving equal pixel areas and arranging pixel centers along lines of constant latitude to support efficient computation. In engineering and computational science, HEALPix pixelation helps manage spherical datasets, including directional measurements, simulations, and spatial maps, by providing standardized indexing, scalable resolution, and reliable comparisons between regions. Its structure supports fast neighborhood searches, visualization, and numerical analysis of data on curved surfaces.

Healpix Pixelation - Related Videos

Research

JoVE Journal - Bioengineering

Lensfree On-chip Tomographic Microscopy Employing Multi-angle Illumination and Pixel Super-resolution

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Cited by 11 •

2012

Lensfree optical tomography is a three-dimensional microscopy technique that offers a spatial resolution of <1 μm × <1 μm × <3 μm in x, y and z dimensions, respectively, over a large imaging-volume of 15-100 mm3, which can be particularly useful for integration with lab-on-a-chip platforms.

Research

JoVE Journal - Bioengineering
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CRISPR/Cas12a Multiplex Genome Editing of Saccharomyces cerevisiae and the Creation of Yeast Pixel Art

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Cited by 11 •

2019

The CRISPR/Cas12a system in combination with a single crRNA array enables efficient multiplex editing of the S. cerevisiae genome at multiple loci simultaneously. This is demonstrated by constructing carotenoid producing yeast strains which are subsequently used to create yeast pixel art.

Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells

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Cited by 17 •

2012

Fluorescence Lifetime Imaging (FLIM) has emerged as a key technique to image the environment and interaction of specific proteins and dyes in living cells. FLIM of fluorescent molecular rotors allows mapping of viscosity in living cells.

A Morphometric and Cellular Analysis Method for the Murine Mandibular Condyle

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Cited by 4 •

2018

This manuscript presents methods for analyzing morphometric and cellular changes within the mandibular condyle of rodents.

Clock Scan Protocol for Image Analysis: ImageJ Plugins

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Cited by 16 •

2017

This paper describes two novel ImageJ plugins for 'Clock Scan' image analysis. These plugins expand the functionality of the original visual basic 6 program and, most importantly, make the program available to a large research community by bundling it with the ImageJ free image analysis software package.

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