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Anna Wierczeiko

dblp:370/5913 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2024
0000-0003-0684-926XORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 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.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 5 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
deep learning-based segmentation
0.812024
ViNe-Seg: deep-learning-assisted segmentation of visible neurons and subsequent analysis embedded in a graphical user interface · Bioinform. 2024
Bioinformatics and computational biology › bioimage informatics › cell segmentation
neuron segmentation
0.812024
ViNe-Seg: deep-learning-assisted segmentation of visible neurons and subsequent analysis embedded in a graphical user interface · Bioinform. 2024
Bioinformatics and computational biology › sequence analysis
nanopore sequencing
0.712023
NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis · Bioinform. 2023
Bioinformatics and computational biology › sequence analysis › nanopore sequencing
real-time sequencing analysis
0.712023
NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis · Bioinform. 2023
Bioinformatics and computational biology
transcriptomics
0.712023
NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis · Bioinform. 2023

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

graphical user interface · 1.4deep learning · 0.8r shiny · 0.7nextflow pipeline · 0.7
YearPublicationVenuePosition
2024 ViNe-Seg: deep-learning-assisted segmentation of visible neurons and subsequent analysis embedded in a graphical user interface
abstract
SUMMARY: Segmentation of neural somata is a crucial and usually the most time-consuming step in the analysis of optical functional imaging of neuronal microcircuits. In recent years, multiple auto-segmentation tools have been developed to improve the speed and consistency of the segmentation process, mostly, using deep learning approaches. Current segmentation tools, while advanced, still encounter challenges in producing accurate segmentation results, especially in datasets with a low signal-to-noise ratio. This has led to a reliance on manual segmentation techniques. However, manual methods, while customized to specific laboratory protocols, can introduce variability due to individual differences in interpretation, potentially affecting dataset consistency across studies. In response to this challenge, we present ViNe-Seg: a deep-learning-based semi-automatic segmentation tool that offers (i) detection of visible neurons, irrespective of their activity status; (ii) the ability to perform segmentation during an ongoing experiment; (iii) a user-friendly graphical interface that facilitates expert supervision, ensuring precise identification of Regions of Interest; (iv) an array of segmentation models with the option of training custom models and sharing them with the community; and (v) seamless integration of subsequent analysis steps. AVAILABILITY AND IMPLEMENTATION: ViNe-Seg code and documentation are publicly available at https://github.com/NiRuff/ViNe-Seg and can be installed from https://pypi.org/project/ViNeSeg/.
Nicolas Ruffini, Saleh Altahini, Stephan Weißbach, Nico Weber, Jonas Milkovits, Anna Wierczeiko, Hendrik Backhaus, Albrecht Stroh
Bioinform.6
2023 NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis
abstract
SUMMARY: Oxford Nanopore Technologies' (ONT) sequencing platform offers an excellent opportunity to perform real-time analysis during sequencing. This feature allows for early insights into experimental data and accelerates a potential decision-making process for further analysis, which can be particularly relevant in the clinical context. Although some tools for the real-time analysis of DNA-sequencing data already exist, there is currently no application available for differential transcriptome data analysis designed for scientists or physicians with limited bioinformatics knowledge. Here, we introduce NanopoReaTA, a user-friendly real-time analysis toolbox for RNA-sequencing data from ONT. Sequencing results from a running or finished experiment are processed through an R Shiny-based graphical user interface with an integrated Nextflow pipeline for whole transcriptome or gene-specific analyses. NanopoReaTA provides visual snapshots of a sequencing run in progress, thus enabling interactive sequencing and rapid decision making that could also be applied to clinical cases. AVAILABILITY AND IMPLEMENTATION: Github https://github.com/AnWiercze/NanopoReaTA; Zenodo https://doi.org/10.5281/zenodo.8099825.
Anna Wierczeiko, Stefan Pastore, Stefan Mündnich, Anne M. Busch, Vincent Dietrich, Mark Helm, Tamer Butto, Susanne Gerber
Bioinform.1