%0 Journal Article %1 Qiu2011 %A Qiu, Peng %A Simonds, Erin F. %A Bendall, Sean C. %A Gibbs, Jr, Kenneth D %A Bruggner, Robert V. %A Linderman, Michael D. %A Sachs, Karen %A Nolan, Garry P. %A Plevritis, Sylvia K. %D 2011 %J Nat Biotechnol %K R highthroughput facs %N 10 %P 886--891 %R 10.1038/nbt.1991 %T Extracting a cellular hierarchy from high-dimensional cytometry data with SPADE. %U http://dx.doi.org/10.1038/nbt.1991 %V 29 %X The ability to analyze multiple single-cell parameters is critical for understanding cellular heterogeneity. Despite recent advances in measurement technology, methods for analyzing high-dimensional single-cell data are often subjective, labor intensive and require prior knowledge of the biological system. To objectively uncover cellular heterogeneity from single-cell measurements, we present a versatile computational approach, spanning-tree progression analysis of density-normalized events (SPADE). We applied SPADE to flow cytometry data of mouse bone marrow and to mass cytometry data of human bone marrow. In both cases, SPADE organized cells in a hierarchy of related phenotypes that partially recapitulated well-described patterns of hematopoiesis. We demonstrate that SPADE is robust to measurement noise and to the choice of cellular markers. SPADE facilitates the analysis of cellular heterogeneity, the identification of cell types and comparison of functional markers in response to perturbations.

@article{Qiu2011, abstract = {The ability to analyze multiple single-cell parameters is critical for understanding cellular heterogeneity. Despite recent advances in measurement technology, methods for analyzing high-dimensional single-cell data are often subjective, labor intensive and require prior knowledge of the biological system. To objectively uncover cellular heterogeneity from single-cell measurements, we present a versatile computational approach, spanning-tree progression analysis of density-normalized events (SPADE). We applied SPADE to flow cytometry data of mouse bone marrow and to mass cytometry data of human bone marrow. In both cases, SPADE organized cells in a hierarchy of related phenotypes that partially recapitulated well-described patterns of hematopoiesis. We demonstrate that SPADE is robust to measurement noise and to the choice of cellular markers. SPADE facilitates the analysis of cellular heterogeneity, the identification of cell types and comparison of functional markers in response to perturbations.}, added-at = {2013-07-27T01:52:37.000+0200}, author = {Qiu, Peng and Simonds, Erin F. and Bendall, Sean C. and {Gibbs, Jr}, Kenneth D and Bruggner, Robert V. and Linderman, Michael D. and Sachs, Karen and Nolan, Garry P. and Plevritis, Sylvia K.}, biburl = {https://www.bibsonomy.org/bibtex/29f9e779593de80c588910c123de7d417/aorchid}, description = {SPADE from Nolan's lab.}, doi = {10.1038/nbt.1991}, file = {:R/NatBiotechnol.29.886.pdf:PDF}, groups = {public}, institution = {Department of Radiology, Stanford University, Stanford, CA, USA. pqiu@mdanderson.org}, interhash = {8ba6061fbb5eda7f37c4851717ca1622}, intrahash = {9f9e779593de80c588910c123de7d417}, journal = {Nat Biotechnol}, keywords = {R highthroughput facs}, language = {eng}, medline-pst = {epublish}, month = Oct, number = 10, pages = {886--891}, pii = {nbt.1991}, pmid = {21964415}, timestamp = {2013-07-27T01:52:37.000+0200}, title = {Extracting a cellular hierarchy from high-dimensional cytometry data with SPADE.}, url = {http://dx.doi.org/10.1038/nbt.1991}, username = {aorchid}, volume = 29, year = 2011 }