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@ARTICLE{Adameyko:275838,
author = {Adameyko, Igor and Bakken, Trygve and Bhaduri, Aparna and
Chhatbar, Chintan and Filbin, Mariella G and Gate, David and
Hochgerner, Hannah and Kim, Chang Nam and Krull, Jordan and
La Manno, Gioele and Li, Qingyun and Linnarsson, Sten and
Ma, Qin and Mayer, Christian and Menon, Vilas and Nano,
Patricia and Prinz, Marco and Quake, Steve and Walsh,
Christopher A and Yang, Jin and Bayraktar, Omer Ali and
Gokce, Ozgun and Habib, Naomi and Konopka, Genevieve and
Liddelow, Shane A and Nowakowski, Tomasz J},
title = {{A}pplying single-cell and single-nucleus genomics to
studies of cellular heterogeneity and cell fate transitions
in the nervous system.},
journal = {Nature neuroscience},
volume = {27},
number = {12},
issn = {1097-6256},
address = {New York, NY},
publisher = {Nature America},
reportid = {DZNE-2025-00073},
pages = {2278 - 2291},
year = {2024},
abstract = {Single-cell and single-nucleus genomic approaches can
provide unbiased and multimodal insights. Here, we discuss
what constitutes a molecular cell atlas and how to leverage
single-cell omics data to generate hypotheses and gain
insights into cell transitions in development and disease of
the nervous system. We share points of reflection on what to
consider during study design and implementation as well as
limitations and pitfalls.},
subtyp = {Review Article},
keywords = {Animals / Humans / Cell Differentiation: genetics / Cell
Nucleus: metabolism / Cell Nucleus: genetics / Genomics:
methods / Nervous System: cytology / Nervous System:
metabolism / Single-Cell Analysis: methods},
cin = {AG Gokce},
ddc = {610},
cid = {I:(DE-2719)1013041},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39627588},
doi = {10.1038/s41593-024-01827-9},
url = {https://pub.dzne.de/record/275838},
}