Part of the flow/mass cytometry data analysis process is aligning (matching) cell subsets between relevant samples. Current methods address this cluster-matching problem in ways that are either computationally expensive, affected by the curse of dimensionality, or fail when population patterns significantly vary between samples. Here, we introduce a quadratic form (QF)-based cluster matching algorithm (QFMatch) that is computationally efficient and accommodates cases where population locations differ significantly (or even disappear or appear) from sample to sample. We demonstrate the effectiveness of QFMatch by evaluating sample datasets from immunology studies. The algorithm is based on a novel multivariate extension of the quadratic form...
Background Clinical flow cytometry typically involves the sequential interpretation of two-dimensio...
<div><p>In biomedical applications, an experimenter encounters different potential sources of variat...
Background: As a high-throughput technology that offers rapid quantification of mul...
Part of the flow/mass cytometry data analysis process is aligning (matching) cell subsets between re...
We present an algorithm for modeling flow cytometry data in the presence of large inter-sample varia...
Recent technological developments in high-dimensional flow cytometry and mass cytometry (CyTOF) have...
Flow cytometry (FC) is a single-cell profiling platform for measuring the phenotypes (protein expres...
Flow cytometry is a technology that rapidly measures antigen-based markers associated to cells in a ...
Background: The capability of flow cytometry to offer rapid quantification of multidimensional chara...
Flow cytometry is widely used for single cell interrogation of surface and intracellular protein exp...
In systems biomedicine, an experimenter encounters different potential sources of vari-ation in data...
In biomedical applications, an experimenter encounters different potential sources of variation in d...
The introduction of single-cell platforms inspired the development of high-dimensional single-cell a...
In biomedical applications, an experimenter encounters different potential sources of variation in d...
International audienceBackground: Cytometry is an experimental technique used to measure molecules e...
Background Clinical flow cytometry typically involves the sequential interpretation of two-dimensio...
<div><p>In biomedical applications, an experimenter encounters different potential sources of variat...
Background: As a high-throughput technology that offers rapid quantification of mul...
Part of the flow/mass cytometry data analysis process is aligning (matching) cell subsets between re...
We present an algorithm for modeling flow cytometry data in the presence of large inter-sample varia...
Recent technological developments in high-dimensional flow cytometry and mass cytometry (CyTOF) have...
Flow cytometry (FC) is a single-cell profiling platform for measuring the phenotypes (protein expres...
Flow cytometry is a technology that rapidly measures antigen-based markers associated to cells in a ...
Background: The capability of flow cytometry to offer rapid quantification of multidimensional chara...
Flow cytometry is widely used for single cell interrogation of surface and intracellular protein exp...
In systems biomedicine, an experimenter encounters different potential sources of vari-ation in data...
In biomedical applications, an experimenter encounters different potential sources of variation in d...
The introduction of single-cell platforms inspired the development of high-dimensional single-cell a...
In biomedical applications, an experimenter encounters different potential sources of variation in d...
International audienceBackground: Cytometry is an experimental technique used to measure molecules e...
Background Clinical flow cytometry typically involves the sequential interpretation of two-dimensio...
<div><p>In biomedical applications, an experimenter encounters different potential sources of variat...
Background: As a high-throughput technology that offers rapid quantification of mul...