Scaling single-cell genomics from phenomenology to mechanism

Three of the most fundamental questions in biology are how individual cells differentiate to form tissues, how tissues function in a coordinated and flexible fashion and which gene regulatory mechanisms support these processes. Single-cell genomics is opening up new ways to tackle these questions by...

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Main Authors: Tanay, Amos, Regev, Aviv
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Published: Nature Publishing Group 2018
Online Access:http://hdl.handle.net/1721.1/116803
https://orcid.org/0000-0001-8567-2049
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author Tanay, Amos
Regev, Aviv
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Tanay, Amos
Regev, Aviv
author_sort Tanay, Amos
collection MIT
description Three of the most fundamental questions in biology are how individual cells differentiate to form tissues, how tissues function in a coordinated and flexible fashion and which gene regulatory mechanisms support these processes. Single-cell genomics is opening up new ways to tackle these questions by combining the comprehensive nature of genomics with the microscopic resolution that is required to describe complex multicellular systems. Initial single-cell genomic studies provided a remarkably rich phenomenology of heterogeneous cellular states, but transforming observational studies into models of dynamics and causal mechanisms in tissues poses fresh challenges and requires stronger integration of theoretical, computational and experimental frameworks.
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spelling mit-1721.1/1168032022-10-03T08:45:56Z Scaling single-cell genomics from phenomenology to mechanism Tanay, Amos Regev, Aviv Massachusetts Institute of Technology. Department of Biology Koch Institute for Integrative Cancer Research at MIT Regev, Aviv Three of the most fundamental questions in biology are how individual cells differentiate to form tissues, how tissues function in a coordinated and flexible fashion and which gene regulatory mechanisms support these processes. Single-cell genomics is opening up new ways to tackle these questions by combining the comprehensive nature of genomics with the microscopic resolution that is required to describe complex multicellular systems. Initial single-cell genomic studies provided a remarkably rich phenomenology of heterogeneous cellular states, but transforming observational studies into models of dynamics and causal mechanisms in tissues poses fresh challenges and requires stronger integration of theoretical, computational and experimental frameworks. 2018-07-05T18:28:28Z 2018-07-05T18:28:28Z 2017-01 2016-09 2018-07-02T18:59:27Z Article http://purl.org/eprint/type/JournalArticle 0028-0836 1476-4687 http://hdl.handle.net/1721.1/116803 Tanay, Amos and Aviv Regev. “Scaling Single-Cell Genomics from Phenomenology to Mechanism.” Nature 541, 7637 (January 2017): 331–338 © 2017 Macmillan Publishers Limited, part of Springer Nature https://orcid.org/0000-0001-8567-2049 http://dx.doi.org/10.1038/NATURE21350 Nature Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf Nature Publishing Group PMC
spellingShingle Tanay, Amos
Regev, Aviv
Scaling single-cell genomics from phenomenology to mechanism
title Scaling single-cell genomics from phenomenology to mechanism
title_full Scaling single-cell genomics from phenomenology to mechanism
title_fullStr Scaling single-cell genomics from phenomenology to mechanism
title_full_unstemmed Scaling single-cell genomics from phenomenology to mechanism
title_short Scaling single-cell genomics from phenomenology to mechanism
title_sort scaling single cell genomics from phenomenology to mechanism
url http://hdl.handle.net/1721.1/116803
https://orcid.org/0000-0001-8567-2049
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