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Kyle Ferchen

dblp:370/4550 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2023
0000-0002-3470-3623ORCID · 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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
cytometry data analysis
0.712023
pyInfinityFlow: optimized imputation and analysis of high-dimensional flow cytometry data for millions of cells · Bioinform. 2023
Bioinformatics and computational biology
single-cell analysis
0.712023
pyInfinityFlow: optimized imputation and analysis of high-dimensional flow cytometry data for millions of cells · Bioinform. 2023
Bioinformatics and computational biology › single-cell analysis
cell population identification
0.212023
pyInfinityFlow: optimized imputation and analysis of high-dimensional flow cytometry data for millions of cells · Bioinform. 2023
Bioinformatics and computational biology › single-cell analysis
rare cell population discovery
0.212023
pyInfinityFlow: optimized imputation and analysis of high-dimensional flow cytometry data for millions of cells · Bioinform. 2023

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

imputation · 0.7
YearPublicationVenuePosition
2023 pyInfinityFlow: optimized imputation and analysis of high-dimensional flow cytometry data for millions of cells
abstract
MOTIVATION: While conventional flow cytometry is limited to dozens of markers, new experimental and computational strategies, such as Infinity Flow, allow for the generation and imputation of hundreds of cell surface protein markers in millions of cells. Here, we describe an end-to-end analysis workflow for Infinity Flow data in Python. RESULTS: pyInfinityFlow enables the efficient analysis of millions of cells, without down-sampling, through direct integration with well-established Python packages for single-cell genomics analysis. pyInfinityFlow accurately identifies both common and extremely rare cell populations which are challenging to define from single-cell genomics studies alone. We demonstrate that this workflow can nominate novel markers to design new flow cytometry gating strategies for predicted cell populations. pyInfinityFlow can be extended to diverse cell discovery analyses with flexibility to adapt to diverse Infinity Flow experimental designs. AVAILABILITY AND IMPLEMENTATION: pyInfinityFlow is freely available in GitHub (https://github.com/KyleFerchen/pyInfinityFlow) and on PyPI (https://pypi.org/project/pyInfinityFlow/). Package documentation with tutorials on a test dataset is available by Read the Docs (pyinfinityflow.readthedocs.io). The scripts and data for reproducing the results are available at https://github.com/KyleFerchen/pyInfinityFlow/tree/main/analysis_scripts, along with the raw flow cytometry input data.
Kyle Ferchen, Nathan Salomonis, H. Leighton Grimes
Bioinform.1