123 machine learning datasets
123 dataset results
MICCAI Challenge on Circuit Reconstruction from Electron Microscopy Images.
Data The data for this Challenge are from multiple sources: CPSC Database and CPSC-Extra Database INCART Database PTB and PTB-XL Database The Georgia 12-lead ECG Challenge (G12EC) Database Undisclosed Database The first source is the public (CPSC Database) and unused data (CPSC-Extra Database) from the China Physiological Signal Challenge in 2018 (CPSC2018), held during the 7th International Conference on Biomedical Engineering and Biotechnology in Nanjing, China. The unused data from the CPSC2018 is NOT the test data from the CPSC2018. The test data of the CPSC2018 is included in the final private database that has been sequestered. This training set consists of two sets of 6,877 (male: 3,699; female: 3,178) and 3,453 (male: 1,843; female: 1,610) of 12-ECG recordings lasting from 6 seconds to 60 seconds. Each recording was sampled at 500 Hz.
The eSports Sensors dataset contains sensor data collected from 10 players in 22 matches in League of Legends. The sensor data collected includes:
CoVERT is a fact-checked corpus of tweets with a focus on the domain of biomedicine and COVID-19-related (mis)information. The corpus consists of 300 tweets, each annotated with medical named entities and relations. Employs a novel crowdsourcing methodology to annotate all tweets with fact-checking labels and supporting evidence, which crowdworkers search for online. This methodology results in moderate inter-annotator agreement.
The LIMUC dataset is the largest publicly available labeled ulcerative colitis dataset that compromises 11276 images from 564 patients and 1043 colonoscopy procedures. Three experienced gastroenterologists were involved in the annotation process, and all images are labeled according to the Mayo endoscopic score (MES).
The second Ninapro database includes 40 intact subjects and it is thoroughly described in the paper: "Manfredo Atzori, Arjan Gijsberts, Claudio Castellini, Barbara Caputo, Anne-Gabrielle Mittaz Hager, Simone Elsig, Giorgio Giatsidis, Franco Bassetto & Henning Müller. Electromyography data for non-invasive naturally-controlled robotic hand prostheses. Scientific Data, 2014" (http://www.nature.com/articles/sdata201453). Please, cite this paper for any work related to the Ninapro database. Please, use also the paper by Gijsberts et al., 2014 (http://publications.hevs.ch/index.php/publications/show/1629) for more information about the database.
Overview This database of simulated arterial pulse waves is designed to be representative of a sample of pulse waves measured from healthy adults. It contains pulse waves for 4,374 virtual subjects, aged from 25-75 years old (in 10 year increments). The database contains a baseline set of pulse waves for each of the six age groups, created using cardiovascular properties (such as heart rate and arterial stiffness) which are representative of healthy subjects at each age group. It also contains 728 further virtual subjects at each age group, in which each of the cardiovascular properties are varied within normal ranges. This allows for extensive in silico analyses of haemodynamics and the performance of pulse wave analysis algorithms.
The “Medico automatic polyp segmentation challenge” aims to develop computer-aided diagnosis systems for automatic polyp segmentation to detect all types of polyps (for example, irregular polyp, smaller or flat polyps) with high efficiency and accuracy. The main goal of the challenge is to benchmark semantic segmentation algorithms on a publicly available dataset, emphasizing robustness, speed, and generalization.
The dataset contains a Video capsule endoscopy dataset for polyp segmentation.
How and where proteins interface with one another can ultimately impact the proteins' functions along with a range of other biological processes. As such, precise computational methods for protein interface prediction (PIP) come highly sought after as they could yield significant advances in drug discovery and design as well as protein function analysis. However, the traditional benchmark dataset for this task, Docking Benchmark 5 (DB5), contains only a paltry 230 complexes for training, validating, and testing different machine learning algorithms. In this work, we expand on a dataset recently introduced for this task, the Database of Interacting Protein Structures (DIPS), to present DIPS-Plus, an enhanced, feature-rich dataset of 42,112 complexes for geometric deep learning of protein interfaces. The previous version of DIPS contains only the Cartesian coordinates and types of the atoms comprising a given protein complex, whereas DIPS-Plus now includes a plethora of new residue-level
By releasing this dataset, we aim at providing a new testbed for computer vision techniques using Deep Learning. The main peculiarity is the shift from the domain of "natural images" proper of common benchmark dataset to biological imaging. We anticipate that the advantages of doing so could be two-fold: i) fostering research in biomedical-related fields - for which popular pre-trained models perform typically poorly - and ii) promoting methodological research in deep learning by addressing peculiar requirements of these images. Possible applications include but are not limited to semantic segmentation, object detection and object counting. The data consist of 283 high-resolution pictures (1600x1200 pixels) of mice brain slices acquired through a fluorescence microscope. The final goal is to individuate and count neurons highlighted in the pictures by means of a marker, so to assess the result of a biological experiment. The corresponding ground-truth labels were generated through a hy
PETRAW data set was composed of 150 sequences of peg transfer training sessions. The objective of the peg transfer session is to transfer 6 blocks from the left to the right and back. Each block must be extracted from a peg with one hand, transferred to the other hand, and inserted in a peg at the other side of the board. All cases were acquired by a non-medical expert on the LTSI Laboratory from the University of Rennes. The data set was divided into a training data set composed of 90 cases and a test data set composed of 60 cases. A case was composed of kinematic data, a video, semantic segmentation of each frame, and workflow annotation.
Placenta is a benchmark dataset for node classification in an underexplored domain: predicting microanatomical tissue structures from cell graphs in placenta histology whole slide images. Cell graphs are large (>1 million nodes per image), node features are varied (64-dimensions of 11 types of cells), class labels are imbalanced (9 classes ranging from 0.21% of the data to 40.0%), and cellular communities cluster into heterogeneously distributed tissues of widely varying sizes (from 11 nodes to 44,671 nodes for a single structure).
PubMedCite is a domain-specific dataset with about 192K biomedical scientific papers and a large citation graph preserving 917K citation relationships between them. It is characterized by preserving the salient contents extracted from full texts of references, and the weighted correlation between the salient.
CheXlocalize is a radiologist-annotated segmentation dataset on chest X-rays. The dataset consists of two types of radiologist annotations for the localization of 10 pathologies: pixel-level segmentations and most-representative points. Annotations were drawn on images from the CheXpert validation and test sets. The dataset also consists of two separate sets of radiologist annotations: (1) ground-truth pixel-level segmentations on the validation and test sets, drawn by two board-certified radiologists, and (2) benchmark pixel-level segmentations and most-representative points on the test set, drawn by a separate group of three board-certified radiologists.
A challenge that consists of three tasks, each targeting a different requirement for in-clinic use. The first task involves classifying images from the GI tract into 23 distinct classes. The second task focuses on efficiant classification measured by the amount of time spent processing each image. The last task relates to automatcially segmenting polyps.
This collection contains data and code associated with the IPCAI/IJCARS 2020 paper “Automatic Annotation of Hip Anatomy in Fluoroscopy for Robust and Efficient 2D/3D Registration.” The data hosted here consists of annotated datasets of actual hip fluoroscopy, CT and derived data from six lower torso cadaveric specimens. Documentation and examples for using the dataset and Python code for training and testing the proposed models are also included. Higher-level information, including clinical motivations, prior works, algorithmic details, applications to 2D/3D registration, and experimental details, may be found in the companion paper which is available at https://arxiv.org/abs/1911.07042 or https://doi.org/10.1007/s11548-020-02162-7. We hope that this code and data will be useful in the development of new computer-assisted capabilities that leverage fluoroscopy.
Kvasir-Capsule dataset is the largest publicly released VCE dataset. In total, the dataset contains 47,238 labeled images and 117 videos, where it captures anatomical landmarks and pathological and normal findings. The results is more than 4,741,621 images and video frames altogether.
This mouse cerebellar atlas can be used for mouse cerebellar morphometry.
This is a set of 100,000 non-overlapping image patches from hematoxylin & eosin (H&E) stained histological images of human colorectal cancer (CRC) and normal tissue. All images are 224x224 pixels (px) at 0.5 microns per pixel (MPP). For tissue classification; the classes are: Adipose (ADI), background (BACK), debris (DEB), lymphocytes (LYM), mucus (MUC), smooth muscle (MUS), normal colon mucosa (NORM), cancer-associated stroma (STR), colorectal adenocarcinoma epithelium (TUM). The images were manually extracted from N=86 H&E stained human cancer tissue slides from formalin-fixed paraffin-embedded (FFPE) samples from the NCT Biobank (National Center for Tumor Diseases, Heidelberg, Germany) and the UMM pathology archive (University Medical Center Mannheim, Mannheim, Germany). Tissue samples contained CRC primary tumor slides and tumor tissue from CRC liver metastases; normal tissue classes were augmented with non-tumorous regions from gastrectomy specimen to increase variability.