Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Harald Stachelscheid

dblp:133/2687 · DBLP profile ↗
← Back
3ranked-venue papers
0as first author
1since 2021 · last 2021
0000-0002-9283-4605ORCID · verified

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 3 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Computer graphics and multimedia
2 papers
Image and video coding · 47% Computational photography and imaging · 47% Visualization and visual analytics · 6%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Image and video coding
image quality assessment
0.512021
FRC-QE: a robust and comparable 3D microscopy image quality metric for cleared organoids · Bioinform. 2021
Computational photography and imaging › microscopy imaging › computational microscopy
microscopy image reconstruction
0.512021
FRC-QE: a robust and comparable 3D microscopy image quality metric for cleared organoids · Bioinform. 2021
Bioinformatics and computational biology › gene expression analysis
gene expression visualization
0.212015
Semantic Body Browser: graphical exploration of an organism and spatially resolved expression data visualization · Bioinform. 2015

Methods — techniques the papers use, named apart from their topics

fourier ring correlation · 0.5
YearPublicationVenuePosition
2021 FRC-QE: a robust and comparable 3D microscopy image quality metric for cleared organoids
abstract
SUMMARY: Here, we propose Fourier ring correlation-based quality estimation (FRC-QE) as a new metric for automated image quality estimation in 3D fluorescence microscopy acquisitions of cleared organoids that yields comparable measurements across experimental replicates, clearing protocols and works for different microscopy modalities. AVAILABILITY AND IMPLEMENTATION: FRC-QE is written in ImgLib2/Java and provided as an easy-to-use and macro-scriptable plugin for Fiji. Code, documentation, sample images and further information can be found under https://github.com/PreibischLab/FRC-QE. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Friedrich Preusser, Natália dos Santos, Jörg Contzen, Harald Stachelscheid, Érico Tosoni Costa, Philipp Mergenthaler, Stephan Preibisch
Bioinform.4
2015 Semantic Body Browser: graphical exploration of an organism and spatially resolved expression data visualization
abstract
UNLABELLED: Advancing technologies generate large amounts of molecular and phenotypic data on cells, tissues and organisms, leading to an ever-growing detail and complexity while information retrieval and analysis becomes increasingly time-consuming. The Semantic Body Browser is a web application for intuitively exploring the body of an organism from the organ to the subcellular level and visualising expression profiles by means of semantically annotated anatomical illustrations. It is used to comprehend biological and medical data related to the different body structures while relying on the strong pattern recognition capabilities of human users. AVAILABILITY AND IMPLEMENTATION: The Semantic Body Browser is a JavaScript web application that is freely available at http://sbb.cellfinder.org. The source code is provided on https://github.com/flekschas/sbb.
Fritz Lekschas, Harald Stachelscheid, Stefanie Seltmann, Andreas Kurtz 0003
Bioinform.2
2013 CELDA - an ontology for the comprehensive representation of cells in complex systems
abstract
BACKGROUND: The need for detailed description and modeling of cells drives the continuous generation of large and diverse datasets. Unfortunately, there exists no systematic and comprehensive way to organize these datasets and their information. CELDA (Cell: Expression, Localization, Development, Anatomy) is a novel ontology for the association of primary experimental data and derived knowledge to various types of cells of organisms. RESULTS: CELDA is a structure that can help to categorize cell types based on species, anatomical localization, subcellular structures, developmental stages and origin. It targets cells in vitro as well as in vivo. Instead of developing a novel ontology from scratch, we carefully designed CELDA in such a way that existing ontologies were integrated as much as possible, and only minimal extensions were performed to cover those classes and areas not present in any existing model. Currently, ten existing ontologies and models are linked to CELDA through the top-level ontology BioTop. Together with 15.439 newly created classes, CELDA contains more than 196.000 classes and 233.670 relationship axioms. CELDA is primarily used as a representational framework for modeling, analyzing and comparing cells within and across species in CellFinder, a web based data repository on cells (http://cellfinder.org). CONCLUSIONS: CELDA can semantically link diverse types of information about cell types. It has been integrated within the research platform CellFinder, where it exemplarily relates cell types from liver and kidney during development on the one hand and anatomical locations in humans on the other, integrating information on all spatial and temporal stages. CELDA is available from the CellFinder website: http://cellfinder.org/about/ontology.
Stefanie Seltmann, Harald Stachelscheid, Alexander Damaschun, Ludger Jansen, Fritz Lekschas, Jean-Fred Fontaine, Throng-Nghia Nguyen-Dobinsky, Ulf Leser, Andreas Kurtz 0003
BMC Bioinform.2