Synaptic partner prediction from point annotations in insect brains

High-throughput electron microscopy allows recording of lar- ge stacks of neural tissue with sufficient resolution to extract the wiring diagram of the underlying neural network. Current efforts to automate this process focus mainly on the segmentation of neurons. However, in order to recover a wiring diagram, synaptic partners need to be identi- fied as well. This is especially challenging in insect brains like Drosophila melanogaster, where one presynaptic site is associated with multiple post- synaptic elements. Here we propose a 3D U-Net architecture to directly identify pairs of voxels that are pre- and postsynaptic to each other. To that end, we formulate the problem of synaptic partner identification as a classification problem on long-range edges between voxels to encode both the presence of a synaptic pair and its direction. This formulation allows us to directly learn from synaptic point annotations instead of more ex- pensive voxel-based synaptic cleft or vesicle annotations. We evaluate our method on the MICCAI 2016 CREMI challenge and improve over the current state of the art, producing 3% fewer errors than the next best method

Domain adaptive segmentation in volume electron microscopy imaging

In the last years, automated segmentation has become a necessary tool for volume electron microscopy (EM) imaging. So far, the best performing techniques have been largely based on fully supervised encoder-decoder CNNs, requiring a substantial amount of annotated images. Domain Adaptation (DA) aims to alleviate the annotation burden by 'adapting' the networks trained on existing groundtruth data (source domain) to work on a different (target) domain with as little additional annotation as possible. Most DA research is focused on the classification task, whereas volume EM segmentation remains rather unexplored. In this work, we extend recently proposed classification DA techniques to an encoder-decoder layout and propose a novel method that adds a reconstruction decoder to the classical encoder-decoder segmentation in order to align source and target encoder features. The method has been validated on the task of segmenting mitochondria in EM volumes. We have performed DA from brain EM images to HeLa cells and from isotropic FIB/SEM volumes to anisotropic TEM volumes. In all cases, the proposed method has outperformed the extended classification DA techniques and the finetuning baseline. An implementation of our work can be found on https://github.com/JorisRoels/domain-adaptive-segmentation

Synaptic Cleft Segmentation in Non-Isotropic Volume Electron Microscopy of the Complete Drosophila Brain

Neural circuit reconstruction at single synapse resolution is increasingly recognized as crucially important to decipher the function of biological nervous systems. Volume electron microscopy in serial transmission or scanning mode has been demonstrated to provide the necessary resolution to segment or trace all neurites and to annotate all synaptic connections. Automatic annotation of synaptic connections has been done successfully in near isotropic electron microscopy of vertebrate model organisms. Results on non-isotropic data in insect models, however, are not yet on par with human annotation. We designed a new 3D-U-Net architecture to optimally represent isotropic fields of view in non-isotropic data. We used regression on a signed distance transform of manually annotated synaptic clefts of the CREMI challenge dataset to train this model and observed significant improvement over the state of the art. We developed open source software for optimized parallel prediction on very large volumetric datasets and applied our model to predict synaptic clefts in a 50 tera-voxels dataset of the complete Drosophila brain. Our model generalizes well to areas far away from where training data was available

Automated Analysis of Biomedical Data from Low to High Resolution

Recent developments of experimental techniques and instrumentation allow life scientists to acquire enormous volumes of data at unprecedented resolution. While this new data brings much deeper insight into cellular processes, it renders manual analysis infeasible and calls for the development of new, automated analysis procedures. This thesis describes how methods of pattern recognition can be used to automate three popular data analysis protocols: Chapter 1 proposes a method to automatically locate bimodal isotope distribution patterns in Hydrogen Deuterium Exchange Mass Spectrometry experiments. The method is based on L1-regularized linear regression and allows for easy quantitative analysis of co-populations with different exchange behavior. The sensitivity of the method is tested on a set of manually identified peptides, while its applicability to exploratory data analysis is validated by targeted follow-up peptide identification. Chapter 2 develops a technique to automate peptide quantification for mass spectrometry experiments, based on 16O/18O labeling of peptides. Two different spectrum segmentation algorithms are proposed: one based on image processing and applicable to low resolution data and one exploiting the sparsity of high resolution data. The quantification accuracy is validated on calibration datasets, produced by mixing a set of proteins in pre-defined ratios. Chapter 3 provides a method for automated detection and segmentation of synapses in electron microscopy images of neural tissue. For images acquired by scanning electron microscopy with nearly isotropic resolution, the algorithm is based on geometric features computed in 3D pixel neighborhoods. For transmission electron microscopy images with poor z-resolution, the algorithm uses additional regularization by performing several rounds of pixel classification with features computed on the probability maps of the previous classification round. The validation is performed by comparing the set of synapses detected by the algorithm against a gold standard detection by human experts. For data with nearly isotropic resolution, the algorithm performance is comparable to that of the human experts

Domain Adaptive Segmentation in Volume Electron Microscopy Imaging

In the last years, automated segmentation has become a necessary tool for volume electron microscopy (EM) imaging. So far, the best performing techniques have been largely based on fully supervised encoder-decoder CNNs, requiring a substantial amount of annotated images. Domain Adaptation (DA) aims to alleviate the annotation burden by 'adapting' the networks trained on existing groundtruth data (source domain) to work on a different (target) domain with as little additional annotation as possible. Most DA research is focused on the classification task, whereas volume EM segmentation remains rather unexplored. In this work, we extend recently proposed classification DA techniques to an encoder-decoder layout and propose a novel method that adds a reconstruction decoder to the classical encoder-decoder segmentation in order to align source and target encoder features. The method has been validated on the task of segmenting mitochondria in EM volumes. We have performed DA from brain EM images to HeLa cells and from isotropic FIB/SEM volumes to anisotropic TEM volumes. In all cases, the proposed method has outperformed the extended classification DA techniques and the finetuning baseline. An implementation of our work can be found on https://github.com/JorisRoels/domain-adaptive-segmentation.Comment: ISBI 2019 (accepted

ROOT Statistical Software

Advanced mathematical and statistical computational methods are required by the LHC experiments for analyzing their data. Some of these methods are provided by the ROOT project, a C++ Object Oriented framework for large scale data handling applications. We review the current mathematical and statistical classes present in ROOT, emphasizing the recent developments