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Florian Buettner

Publications and source records attributed to Florian Buettner.

3 recordsLinked to original sources

cgCorrect: A method to correct for confounding cell-cell variation due to cell growth in single-cell transcriptomics

Motivation: Accessing gene expression at the single cell level has unraveled often large heterogeneity among seemingly homogeneous cells, which remained obscured in traditional population based approaches. The computational analysis of single-cell transcriptomics data, however, still imposes unresolved challenges with respect to normalization, visualization and modeling the data. One such issue are differences in cell size, which introduce additional variability into the data, for which appropriate normalization techniques are needed. Otherwise, these differences in cell size may obscure genuine heterogeneities among cell populations and lead to overdispersed steady-state distributions of mRNA transcript numbers.\n\nResults: We present cgCorrect, a statistical framework to correct for differences in cell size that are due to cell growth in single-cell transcriptomics data. We derive the probability for the cell growth corrected mRNA transcript number given the measured, cell size dependent mRNA transcript number, based on the assumption that the average number of transcripts in a cell increases proportional to the cells volume during cell cycle. cgCorrect can be used for both data normalization, and to analyze steady-state distributions used to infer the gene expression mechanism. We demonstrate its applicability on both simulated data and single-cell quantitative real-time PCR data from mouse blood stem and progenitor cells. We show that correcting for differences in cell size affects the interpretation of the data obtained by typically performed computational analysis.\n\nAvailability: A Matlab implementation of cgCorrect is available at http://icb.helmholtz-muenchen.de/cgCorrect\n\nSupplementary information: Supplementary information are available online. The simulated data set is available at http://icb.helmholtz-muenchen.de/cgCorrect

Bioinformatics

Diffusion pseudotime robustly reconstructs lineage branching

Single-cell gene expression profiles of differentiating cells encode their intrinsic latent temporal order. We describe an efficient way to robustly estimate this order according to a diffusion pseudotime, which measures transitions on all length scales between cells using diffusion-like random walks. This allows us to identify cells that undergo branching decisions or are in metastable states, and thereby genes differentially regulated at these states.

Bioinformatics

destiny – diffusion maps for large-scale single-cell data in R

SummaryDiffusion maps are a spectral method for non-linear dimension reduction and have recently been adapted for the visualization of single cell expression data. Here we present destiny, an efficient R implementation of the diffusion map algorithm. Our package includes a single-cell specific noise model allowing for missing and censored values. In contrast to previous implementations, we further present an efficient nearest-neighbour approximation that allows for the processing of hundreds of thousands of cells and a functionality for projecting new data on existing diffusion maps. We exemplarily apply destiny to a recent time-resolved mass cytometry dataset of cellular reprogramming.\n\nAvailability and implementationdestiny is an open-source R/Bioconductor package http://bioconductor.org/packages/ destiny also available at https://www.helmholtz-muenchen.de/icb/destiny. A detailed vignette describing functions and workflows is provided with the package.\n\nContactcarsten.marr@helmholtz-muenchen.de, f.buettner@helmholtz-muenchen.de

Bioinformatics