3,815 research outputs found
A benchmark for epithelial cell tracking
Segmentation and tracking of epithelial cells in light microscopy (LM) movies of developing tissue is an abundant task in cell- and developmental biology. Epithelial cells are densely packed cells that form a honeycomb-like grid. This dense packing distinguishes membrane-stained epithelial cells from the types of objects recent cell tracking benchmarks have focused on, like cell nuclei and freely moving individual cells. While semi-automated tools for segmentation and tracking of epithelial cells are available to biologists, common tools rely on classical watershed based segmentation and engineered tracking heuristics, and entail a tedious phase of manual curation. However, a different kind of densely packed cell imagery has become a focus of recent computer vision research, namely electron microscopy (EM) images of neurons. In this work we explore the benefits of two recent neuron EM segmentation methods for epithelial cell tracking in light microscopy. In particular we adapt two different deep learning approaches for neuron segmentation, namely Flood Filling Networks and MALA, to epithelial cell tracking. We benchmark these on a dataset of eight movies with up to 200 frames. We compare to Moral Lineage Tracing, a combinatorial optimization approach that recently claimed state of the art results for epithelial cell tracking. Furthermore, we compare to Tissue Analyzer, an off-the-shelf tool used by Biologists that serves as our baseline
Fuzzy-based Propagation of Prior Knowledge to Improve Large-Scale Image Analysis Pipelines
Many automatically analyzable scientific questions are well-posed and offer a
variety of information about the expected outcome a priori. Although often
being neglected, this prior knowledge can be systematically exploited to make
automated analysis operations sensitive to a desired phenomenon or to evaluate
extracted content with respect to this prior knowledge. For instance, the
performance of processing operators can be greatly enhanced by a more focused
detection strategy and the direct information about the ambiguity inherent in
the extracted data. We present a new concept for the estimation and propagation
of uncertainty involved in image analysis operators. This allows using simple
processing operators that are suitable for analyzing large-scale 3D+t
microscopy images without compromising the result quality. On the foundation of
fuzzy set theory, we transform available prior knowledge into a mathematical
representation and extensively use it enhance the result quality of various
processing operators. All presented concepts are illustrated on a typical
bioimage analysis pipeline comprised of seed point detection, segmentation,
multiview fusion and tracking. Furthermore, the functionality of the proposed
approach is validated on a comprehensive simulated 3D+t benchmark data set that
mimics embryonic development and on large-scale light-sheet microscopy data of
a zebrafish embryo. The general concept introduced in this contribution
represents a new approach to efficiently exploit prior knowledge to improve the
result quality of image analysis pipelines. Especially, the automated analysis
of terabyte-scale microscopy data will benefit from sophisticated and efficient
algorithms that enable a quantitative and fast readout. The generality of the
concept, however, makes it also applicable to practically any other field with
processing strategies that are arranged as linear pipelines.Comment: 39 pages, 12 figure
A neuronal network of mitochondrial dynamics regulates metastasis.
The role of mitochondria in cancer is controversial. Using a genome-wide shRNA screen, we now show that tumours reprogram a network of mitochondrial dynamics operative in neurons, including syntaphilin (SNPH), kinesin KIF5B and GTPase Miro1/2 to localize mitochondria to the cortical cytoskeleton and power the membrane machinery of cell movements. When expressed in tumours, SNPH inhibits the speed and distance travelled by individual mitochondria, suppresses organelle dynamics, and blocks chemotaxis and metastasis, in vivo. Tumour progression in humans is associated with downregulation or loss of SNPH, which correlates with shortened patient survival, increased mitochondrial trafficking to the cortical cytoskeleton, greater membrane dynamics and heightened cell invasion. Therefore, a SNPH network regulates metastatic competence and may provide a therapeutic target in cancer
ARTMAP-IC and Medical Diagnosis: Instance Counting and Inconsistent Cases
For complex database prediction problems such as medical diagnosis, the ARTMAP-IC neural network adds distributed prediction and category instance counting to the basic fuzzy ARTMAP system. For the ARTMAP match tracking algorithm, which controls search following a predictive error, a new version facilitates prediction with sparse or inconsistent data. Compared to the original match tracking algorithm (MT+), the new algorithm (MT-) better approximates the real-time network differential equations and further compresses memory without loss of performance. Simulations examine predictive accuracy on four medical databases: Pima Indian diabetes, breast cancer, heart disease, and gall bladder removal. ARTMAP-IC results arc equal to or better than those of logistic regression, K nearest neighbor (KNN), the ADAP perceptron, multisurface pattern separation, CLASSIT, instance-based (IBL), and C4. ARTMAP dynamics are fast, stable, and scalable. A voting strategy improves prediction by training the system several times on different orderings of an input set. Voting, instance counting, and distributed representations combine to form confidence estimates for competing predictions.National Science Foundation (IRI 94-01659); Office of Naval Research (N00014-95-J-0409, N00014-95-0657
Robust cell tracking in epithelial tissues through identification of maximum common subgraphs
Tracking of cells in live-imaging microscopy videos of epithelial sheets is a powerful tool for investigating fundamental processes in embryonic development. Characterizing cell growth, proliferation, intercalation and apoptosis in epithelia helps us to understand how morphogenetic processes such as tissue invagination and extension are locally regulated and controlled. Accurate cell tracking requires correctly resolving cells entering or leaving the field of view between frames, cell neighbour exchanges, cell removals and cell divisions. However, current tracking methods for epithelial sheets are not robust to large morphogenetic deformations and require significant manual interventions. Here, we present a novel algorithm for epithelial cell tracking, exploiting the graph-theoretic concept of a ‘maximum common subgraph’ to track cells between frames of a video. Our algorithm does not require the adjustment of tissue-specific parameters, and scales in sub-quadratic time with tissue size. It does not rely on precise positional information, permitting large cell movements between frames and enabling tracking in datasets acquired at low temporal resolution due to experimental constraints such as phototoxicity. To demonstrate the method, we perform tracking on the Drosophila embryonic epidermis and compare cell–cell rearrangements to previous studies in other tissues. Our implementation is open source and generally applicable to epithelial tissues
Efficient Algorithms for Moral Lineage Tracing
Lineage tracing, the joint segmentation and tracking of living cells as they
move and divide in a sequence of light microscopy images, is a challenging
task. Jug et al. have proposed a mathematical abstraction of this task, the
moral lineage tracing problem (MLTP), whose feasible solutions define both a
segmentation of every image and a lineage forest of cells. Their branch-and-cut
algorithm, however, is prone to many cuts and slow convergence for large
instances. To address this problem, we make three contributions: (i) we devise
the first efficient primal feasible local search algorithms for the MLTP, (ii)
we improve the branch-and-cut algorithm by separating tighter cutting planes
and by incorporating our primal algorithms, (iii) we show in experiments that
our algorithms find accurate solutions on the problem instances of Jug et al.
and scale to larger instances, leveraging moral lineage tracing to practical
significance.Comment: Accepted at ICCV 201
CellTag Indexing: Genetic barcode-based sample multiplexing for single-cell genomics
High-throughput single-cell assays increasingly require special consideration in experimental design, sample multiplexing, batch effect removal, and data interpretation. Here, we describe a lentiviral barcode-based multiplexing approach, CellTag Indexing, which uses predefined genetic barcodes that are heritable, enabling cell populations to be tagged, pooled, and tracked over time in the same experimental replicate. We demonstrate the utility of CellTag Indexing by sequencing transcriptomes using a variety of cell types, including long-term tracking of cell engraftment and differentiation in vivo. Together, this presents CellTag Indexing as a broadly applicable genetic multiplexing tool that is complementary with existing single-cell technologies
Computational illumination for high-speed in vitro Fourier ptychographic microscopy
We demonstrate a new computational illumination technique that achieves large
space-bandwidth-time product, for quantitative phase imaging of unstained live
samples in vitro. Microscope lenses can have either large field of view (FOV)
or high resolution, not both. Fourier ptychographic microscopy (FPM) is a new
computational imaging technique that circumvents this limit by fusing
information from multiple images taken with different illumination angles. The
result is a gigapixel-scale image having both wide FOV and high resolution,
i.e. large space-bandwidth product (SBP). FPM has enormous potential for
revolutionizing microscopy and has already found application in digital
pathology. However, it suffers from long acquisition times (on the order of
minutes), limiting throughput. Faster capture times would not only improve
imaging speed, but also allow studies of live samples, where motion artifacts
degrade results. In contrast to fixed (e.g. pathology) slides, live samples are
continuously evolving at various spatial and temporal scales. Here, we present
a new source coding scheme, along with real-time hardware control, to achieve
0.8 NA resolution across a 4x FOV with sub-second capture times. We propose an
improved algorithm and new initialization scheme, which allow robust phase
reconstruction over long time-lapse experiments. We present the first FPM
results for both growing and confluent in vitro cell cultures, capturing videos
of subcellular dynamical phenomena in popular cell lines undergoing division
and migration. Our method opens up FPM to applications with live samples, for
observing rare events in both space and time
Taking aim at moving targets in computational cell migration
Cell migration is central to the development and maintenance of multicellular organisms. Fundamental understanding of cell migration can, for example, direct novel therapeutic strategies to control invasive tumor cells. However, the study of cell migration yields an overabundance of experimental data that require demanding processing and analysis for results extraction. Computational methods and tools have therefore become essential in the quantification and modeling of cell migration data. We review computational approaches for the key tasks in the quantification of in vitro cell migration: image pre-processing, motion estimation and feature extraction. Moreover, we summarize the current state-of-the-art for in silico modeling of cell migration. Finally, we provide a list of available software tools for cell migration to assist researchers in choosing the most appropriate solution for their needs
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