Wiring together large single-cell RNA-seq sample collections

Research output: Working paper

Standard

Wiring together large single-cell RNA-seq sample collections. / Barkas, Nikolas; Petukhov, Viktor; Nikolaeva, Daria; Lozinsky, Yaroslav; Demharter, Samuel; Khodosevich, Konstantin; Kharchenko, Peter V .

Biorxiv : Cold Spring Harbor Laboratory, 2018.

Research output: Working paper

Harvard

Barkas, N, Petukhov, V, Nikolaeva, D, Lozinsky, Y, Demharter, S, Khodosevich, K & Kharchenko, PV 2018 'Wiring together large single-cell RNA-seq sample collections' Cold Spring Harbor Laboratory, Biorxiv. https://doi.org/10.1101/460246

APA

Barkas, N., Petukhov, V., Nikolaeva, D., Lozinsky, Y., Demharter, S., Khodosevich, K., & Kharchenko, P. V. (2018). Wiring together large single-cell RNA-seq sample collections. Cold Spring Harbor Laboratory. https://doi.org/10.1101/460246

Vancouver

Barkas N, Petukhov V, Nikolaeva D, Lozinsky Y, Demharter S, Khodosevich K et al. Wiring together large single-cell RNA-seq sample collections. Biorxiv: Cold Spring Harbor Laboratory. 2018. https://doi.org/10.1101/460246

Author

Barkas, Nikolas ; Petukhov, Viktor ; Nikolaeva, Daria ; Lozinsky, Yaroslav ; Demharter, Samuel ; Khodosevich, Konstantin ; Kharchenko, Peter V . / Wiring together large single-cell RNA-seq sample collections. Biorxiv : Cold Spring Harbor Laboratory, 2018.

Bibtex

@techreport{d9802e4f539145fa95dda7f3d7d6daa0,
title = "Wiring together large single-cell RNA-seq sample collections",
abstract = "Single-cell RNA-seq methods are being increasingly applied in complex study designs, which involve measurements of many samples, commonly spanning multiple individuals, conditions, or tissue compartments. Joint analysis of such extensive, and often heterogeneous, sample collections requires a way of identifying and tracking recurrent cell subpopulations across the entire collection. Here we describe a flexible approach, called Conos (Clustering On Network Of Samples), that relies on multiple plausible inter-sample mappings to construct a global graph connecting all measured cells. The graph can then be used to propagate information between samples and to identify cell communities that show consistent grouping across broad subsets of the collected samples. Conos results enable investigators to balance between resolution and breadth of the detected subpopulations. In this way, it is possible to focus on the fine-grained clusters appearing within more similar subsets of samples, or analyze coarser clusters spanning broader sets of samples in the collection. Such multi-resolution joint clustering provides an important basis for downstream analysis and interpretation of sizable multi-sample single-cell studies and atlas-scale collections.",
author = "Nikolas Barkas and Viktor Petukhov and Daria Nikolaeva and Yaroslav Lozinsky and Samuel Demharter and Konstantin Khodosevich and Kharchenko, {Peter V}",
year = "2018",
doi = "10.1101/460246",
language = "English",
publisher = "Cold Spring Harbor Laboratory",
type = "WorkingPaper",
institution = "Cold Spring Harbor Laboratory",

}

RIS

TY - UNPB

T1 - Wiring together large single-cell RNA-seq sample collections

AU - Barkas, Nikolas

AU - Petukhov, Viktor

AU - Nikolaeva, Daria

AU - Lozinsky, Yaroslav

AU - Demharter, Samuel

AU - Khodosevich, Konstantin

AU - Kharchenko, Peter V

PY - 2018

Y1 - 2018

N2 - Single-cell RNA-seq methods are being increasingly applied in complex study designs, which involve measurements of many samples, commonly spanning multiple individuals, conditions, or tissue compartments. Joint analysis of such extensive, and often heterogeneous, sample collections requires a way of identifying and tracking recurrent cell subpopulations across the entire collection. Here we describe a flexible approach, called Conos (Clustering On Network Of Samples), that relies on multiple plausible inter-sample mappings to construct a global graph connecting all measured cells. The graph can then be used to propagate information between samples and to identify cell communities that show consistent grouping across broad subsets of the collected samples. Conos results enable investigators to balance between resolution and breadth of the detected subpopulations. In this way, it is possible to focus on the fine-grained clusters appearing within more similar subsets of samples, or analyze coarser clusters spanning broader sets of samples in the collection. Such multi-resolution joint clustering provides an important basis for downstream analysis and interpretation of sizable multi-sample single-cell studies and atlas-scale collections.

AB - Single-cell RNA-seq methods are being increasingly applied in complex study designs, which involve measurements of many samples, commonly spanning multiple individuals, conditions, or tissue compartments. Joint analysis of such extensive, and often heterogeneous, sample collections requires a way of identifying and tracking recurrent cell subpopulations across the entire collection. Here we describe a flexible approach, called Conos (Clustering On Network Of Samples), that relies on multiple plausible inter-sample mappings to construct a global graph connecting all measured cells. The graph can then be used to propagate information between samples and to identify cell communities that show consistent grouping across broad subsets of the collected samples. Conos results enable investigators to balance between resolution and breadth of the detected subpopulations. In this way, it is possible to focus on the fine-grained clusters appearing within more similar subsets of samples, or analyze coarser clusters spanning broader sets of samples in the collection. Such multi-resolution joint clustering provides an important basis for downstream analysis and interpretation of sizable multi-sample single-cell studies and atlas-scale collections.

U2 - 10.1101/460246

DO - 10.1101/460246

M3 - Working paper

BT - Wiring together large single-cell RNA-seq sample collections

PB - Cold Spring Harbor Laboratory

CY - Biorxiv

ER -

ID: 213237543