Demo Data from EDBT 2026 / reviewers in the wild / expert
Jana M. Braunger
dblp:425/8465
· DBLP profile ↗
1ranked-venue papers
1as first author
1since 2021 · last 2024
0000-0003-0820-9987ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
functional genomics |
0.8 | 1 | 2024 | Guide assignment in single-cell CRISPR screens using crispat · Bioinform. 2024 |
Bioinformatics and computational biology › single-cell analysis
single-cell genomics |
0.2 | 1 | 2024 | Guide assignment in single-cell CRISPR screens using crispat · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
python package · 0.8guide assignment strategy comparison · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Guide assignment in single-cell CRISPR screens using crispatabstractMOTIVATION: Pooled single-cell CRISPR screens have emerged as a powerful tool in functional genomics to probe the effect of genetic interventions at scale. A crucial step in the analysis of the resulting data is the assignment of cells to gRNAs corresponding to a specific genetic intervention. However, this step is challenging due to a lack of systematic benchmarks and accessible software to apply and compare different guide assignment strategies. To address this, we here propose crispat (CRISPR guide assignment tool), a Python package to facilitate the choice of a suitable guide assignment strategy for single-cell CRISPR screens. RESULTS: We demonstrate the package on four single-cell CRISPR interference screens at low multiplicity of infection from two studies, where crispat identifies strong differences in the number of assigned cells, downregulation of the target genes and number of discoveries across different guide assignment strategies, highlighting the need for a suitable guide assignment strategy to obtain optimal power in single-cell CRISPR screens. AVAILABILITY AND IMPLEMENTATION: crispat is implemented in python, the source code, installation instructions and tutorials can be found at https://github.com/velten-group/crispat and it can be installed from PyPI (https://pypi.org/project/crispat/). Code to reproduce all findings in this paper is available at https://github.com/velten-group/crispat_analysis, as well as at https://zenodo.org/records/13373265. Jana M. Braunger, Britta Velten |
Bioinform. | 1 |