Abstract The resolution and accuracy of single-molecule localization microscopes (SMLMs) are routinely benchmarked using simulated data, calibration rulers, or comparisons to secondary imaging modalities. However, these methods cannot quantify the nanoscale accuracy of an arbitrary SMLM dataset. Here, we show that by computing localization stability under a well-chosen perturbation with accurate knowledge of the imaging system, we can robustly measure the confidence of individual localizations without ground-truth knowledge of the sample. We demonstrate that our method, termed Wasserstein-induced flux (WIF), measures the accuracy of various reconstruction algorithms directly on experimental 2D and 3D data of microtubules and amyloid fibrils. We further show that WIF confidences can be used to evaluate the mismatch between computational models and imaging data, enhance the accuracy and resolution of reconstructed structures, and discover hidden molecular heterogeneities. As a computational methodology, WIF is broadly applicable to any SMLM dataset, imaging system, and localization algorithm.
more »
« less
Measuring localization confidence for quantifying accuracy and heterogeneity in single-molecule super-resolution microscopy
We present a computational method, termed Wasserstein-induced flux (WIF), to robustly quantify the accuracy of individual localizations within a single-molecule localization microscopy (SMLM) dataset without ground- truth knowledge of the sample. WIF relies on the observation that accurate localizations are stable with respect to an arbitrary computational perturbation. Inspired by optimal transport theory, we measure the stability of individual localizations and develop an efficient optimization algorithm to compute WIF. We demonstrate the advantage of WIF in accurately quantifying imaging artifacts in high-density reconstruction of a tubulin network. WIF represents an advance in quantifying systematic errors with unknown and complex distributions, which could improve a variety of downstream quantitative analyses that rely upon accurate and precise imaging. Furthermore, thanks to its formulation as layers of simple analytical operations, WIF can be used as a loss function for optimizing various computational imaging models and algorithms even without training data.
more »
« less
- Award ID(s):
- 1653777
- PAR ID:
- 10135047
- Date Published:
- Journal Name:
- Proc. SPIE
- Volume:
- 11246
- Page Range / eLocation ID:
- 1124611
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Neuronal synapses transmit electrochemical signals between cells through the coordinated action of presynaptic vesicles, ion channels, scaffolding and adapter proteins, and membrane receptors. In situ structural characterization of numerous synaptic proteins simultaneously through multiplexed imaging facilitates a bottom-up approach to synapse classification and phenotypic description. Objective automation of efficient and reliable synapse detection within these datasets is essential for the high-throughput investigation of synaptic features. Convolutional neural networks can solve this generalized problem of synapse detection, however, these architectures require large numbers of training examples to optimize their thousands of parameters. We propose DoGNet, a neural network architecture that closes the gap between classical computer vision blob detectors, such as Difference of Gaussians (DoG) filters, and modern convolutional networks. DoGNet is optimized to analyze highly multiplexed microscopy data. Its small number of training parameters allows DoGNet to be trained with few examples, which facilitates its application to new datasets without overfitting. We evaluate the method on multiplexed fluorescence imaging data from both primary mouse neuronal cultures and mouse cortex tissue slices. We show that DoGNet outperforms convolutional networks with a low-to-moderate number of training examples, and DoGNet is efficiently transferred between datasets collected from separate research groups. DoGNet synapse localizations can then be used to guide the segmentation of individual synaptic protein locations and spatial extents, revealing their spatial organization and relative abundances within individual synapses. The source code is publicly available: https://github.com/kulikovv/dognet.more » « less
-
Extracting an individual’s knowledge structure is a challenging task as it requires formalization of many concepts and their interrelationships. While there has been significant research on how to represent knowledge to support computational design tasks, there is limited understanding of the knowledge structures of human designers. This understanding is necessary for comprehension of cognitive tasks such as decision making and reasoning, and for improving educational programs. In this paper, we focus on quantifying theory-based causal knowledge, which is a specific type of knowledge held by human designers. We develop a probabilistic graph-based model for representing individuals’ concept-specific causal knowledge for a given theory. We propose a methodology based on probabilistic directed acyclic graphs (DAGs) that uses logistic likelihood function for calculating the probability of a correct response. The approach involves a set of questions for gathering responses from 205 engineering students, and a hierarchical Bayesian approach for inferring individuals’ DAGs from the observed responses. We compare the proposed model to a baseline three-parameter logistic (3PL) model from the item response theory. The results suggest that the graph-based logistic model can estimate individual students’ knowledge graphs. Comparisons with the 3PL model indicate that knowledge assessment is more accurate when quantifying knowledge at the level of causal relations than quantifying it using a scalar ability parameter. The proposed model allows identification of parts of the curriculum that a student struggles with and parts they have already mastered which is essential for remediation.more » « less
-
Abstract Due to its specificity, fluorescence microscopy has become a quintessential imaging tool in cell biology. However, photobleaching, phototoxicity, and related artifacts continue to limit fluorescence microscopy’s utility. Recently, it has been shown that artificial intelligence (AI) can transform one form of contrast into another. We present phase imaging with computational specificity (PICS), a combination of quantitative phase imaging and AI, which provides information about unlabeled live cells with high specificity. Our imaging system allows for automatic training, while inference is built into the acquisition software and runs in real-time. Applying the computed fluorescence maps back to the quantitative phase imaging (QPI) data, we measured the growth of both nuclei and cytoplasm independently, over many days, without loss of viability. Using a QPI method that suppresses multiple scattering, we measured the dry mass content of individual cell nuclei within spheroids. In its current implementation, PICS offers a versatile quantitative technique for continuous simultaneous monitoring of individual cellular components in biological applications where long-term label-free imaging is desirable.more » « less
-
null (Ed.)Abstract Extracting an individual’s knowledge structure is a challenging task as it requires formalization of many concepts and their interrelationships. While there has been significant research on how to represent knowledge to support computational design tasks, there is limited understanding of the knowledge structures of human designers. This understanding is necessary for comprehension of cognitive tasks such as decision making and reasoning, and for improving educational programs. In this paper, we focus on quantifying theory-based causal knowledge, which is a specific type of knowledge held by human designers. We develop a probabilistic graph-based model for representing individuals’ concept-specific causal knowledge for a given theory. We propose a methodology based on probabilistic directed acyclic graphs (DAGs) that uses logistic likelihood function for calculating the probability of a correct response. The approach involves a set of questions for gathering responses from 205 engineering students, and a hierarchical Bayesian approach for inferring individuals’ DAGs from the observed responses. We compare the proposed model to a baseline three-parameter logistic (3PL) model from the item response theory. The results suggest that the graph-based logistic model can estimate individual students’ knowledge graphs. Comparisons with the 3PL model indicate that knowledge assessment is more accurate when quantifying knowledge at the level of causal relations than quantifying it using a scalar ability parameter. The proposed model allows identification of parts of the curriculum that a student struggles with and parts they have already mastered which is essential for remediation.more » « less
An official website of the United States government

