<?xml version='1.0' encoding='UTF-8'?><metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns="http://dublincore.org/documents/dcmi-terms/"><dcterms:title>Supporting Data for: Multifocus microscopy with optical sectioning and extended axial resolution</dcterms:title><dcterms:identifier>https://doi.org/10.18710/J0QX3E</dcterms:identifier><dcterms:creator>Ströhl, Florian</dcterms:creator><dcterms:creator>Hansen, Daniel Henry</dcterms:creator><dcterms:creator>Grifo, Mireia Nager</dcterms:creator><dcterms:creator>Birgisdottir, Åsa Birna</dcterms:creator><dcterms:publisher>DataverseNO</dcterms:publisher><dcterms:issued>2022-09-23</dcterms:issued><dcterms:modified>2023-09-28T22:05:05Z</dcterms:modified><dcterms:description>Multifocus microscopy enables recording of entire volumes in a single camera exposure. In dense samples, multifocus microscopy is severely hampered by background haze. We developed a scalable multifocus method that incorporates optical sectioning and offers improved axial resolution capabilities. In our method, dubbed SOLIS, a dithered oblique light-sheet scans the sample volume during a single exposure, while fluorescence from each illuminated plane in the sample is mapped onto a line on the camera with a multifocus optical element. A synchronized rolling shutter readout realizes optical sectioning. This data set contains example images, volumetric stacks, and timelapse videos that demonstrate the technique on endothelial cells (AF488-phalloidin labelled actin) and uncleared engineered human heart tissue (AF488-TOM20 labelled mitochondria).</dcterms:description><dcterms:subject>Medicine, Health and Life Sciences</dcterms:subject><dcterms:subject>Physics</dcterms:subject><dcterms:subject>multi-focus microscopy</dcterms:subject><dcterms:subject>fluoroscence microscopy</dcterms:subject><dcterms:subject>3D microscopy</dcterms:subject><dcterms:subject>light-sheet microscopy</dcterms:subject><dcterms:subject>optical sectioning</dcterms:subject><dcterms:language>English</dcterms:language><dcterms:isReferencedBy>Ströhl F, Hansen DH, Nàger M, Birgisdottir ÅB. Multifocus microscopy with optical sectioning and high axial resolution. Optica. 2022 9(10), doi, 10.1364/OPTICA.468583, https://doi.org/10.1364/OPTICA.468583</dcterms:isReferencedBy><dcterms:date>2022-09-23</dcterms:date><dcterms:contributor>Ströhl, Florian</dcterms:contributor><dcterms:contributor>Ströhl, Florian</dcterms:contributor><dcterms:contributor>Hansen, Daniel H.</dcterms:contributor><dcterms:contributor>Grifo, Mireia N.</dcterms:contributor><dcterms:contributor>Birgisdottir, Åsa B.</dcterms:contributor><dcterms:dateSubmitted>2022-08-18</dcterms:dateSubmitted><dcterms:temporal>2022-02-14</dcterms:temporal><dcterms:temporal>2022-03-17</dcterms:temporal><dcterms:type>experimental data</dcterms:type><dcterms:license>CC0 1.0</dcterms:license></metadata>