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A dataset containing the coordinates and the ID of 147 cells from wound scratch migration experiment
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A data frame with 11970 rows and 4 columns
BT549 cell trajectories were computed using cellmigRation. Imaging experiments were performed as described by Ghannoum S et al (paper in preparation). Briefly, triple negative breast cancer BT549 cells were cultured in RPMI supplemented with 10 and 1 NucLight green lentivirus (Essen BioScience), and then sorted by fluorescence-activated cell sorting (FACS). GFP-positive cells were seeded at a 1:3 ratio with untransduced BT549 cells in 96-well image-lock plates (EssenBio) at a density of 1000 total cells per well. Once cells reached the desired density, a thin wound was introduced by scratching the cell monolayer. Next, cells were scanned at ten-minute intervals over 24h using an Incucyte S3 Live-Cell microscope (EssenBio) at 10x magnification and a Basler Ace 1920-155um camera with CMOS sensor. TIFF images were imported and processed using the cellmigRation library.
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