Collections / geo-gse264425

geo-gse264425

Datasets2
Size~16.6 GB
TechnologyXenium
Samplehuman · lung
KindPublication
Flag a data issue
10.1038/s41467-024-50281-5 ↗
Python · sddb client
from sddb import Catalog

cohort = Catalog().collection("geo-gse264425")
cohort.members        # the 2 datasets as a table

print(cohort.licenses())              # check the terms before you download

sdatas = cohort.to_dict()             # {uid: SpatialData}, cached locally
# or keep the .zarr files in a folder of your choice:
# sdatas = cohort.to_dict(dest="data/")
Python · lamindb

Needs pip install lamindb and network access to the Lamin database, which is limited during the alpha. If it fails, use the Client tab.

import lamindb as ln

db = ln.DB("scverse/spatialdata-db")
coll = db.Collection.get(key="geo-gse264425")
coll.ordered_artifacts.to_dataframe()   # the 2 members, ordered

# download every member .zarr to the local cache:
paths = [a.cache() for a in coll.ordered_artifacts.all()]
Shell
# sddb client: download every member .zarr into data/
sddb-cli download --collection geo-gse264425 --dest data/

Licenses: 2 NCBI GEO policy

Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticity.

Studying human fetal lungs can inform how developmental defects and disease states alter the function of the lungs. Here, we sequenced >150,000 single cells from 19 healthy human pseudoglandular fetal lung tissues ranging between gestational weeks 10-19. We capture dynamic developmental trajectories from progenitor cells that express abundant levels of the cystic fibrosis conductance transmembrane regulator (CFTR). These cells give rise to multiple specialized epithelial cell types. Combined with spatial transcriptomics, we show temporal regulation of key signalling pathways that may drive the temporal and spatial emergence of specialized epithelial cells including ciliated and pulmonary neuroendocrine cells. Finally, we show that human pluripotent stem cell-derived fetal lung models contain CFTR-expressing progenitor cells that capture similar lineage developmental trajectories as identified in the native tissue. Overall, this study provides a comprehensive single-cell atlas of the developing human lung, outlining the temporal and spatial complexities of cell lineage development and benchmarks fetal lung cultures from human pluripotent stem cell differentiations to similar developmental window.

Open in Vitessce
Xenium
Human lung
Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticity [Xenium]: FFPE archived fetal lung tissue GW15; Xenium (GW 15)
human lung 8.0 GB 864,688 cells 339 genes silver NCBI GEO policy
TechnologyXenium
Organismhuman
Tissuelung
Size8.0 GB
Cells864,688
Genes339
silver NCBI GEO policy Open in Vitessce
Open in Vitessce
Xenium
Human lung
Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticity [Xenium]: FFPE archived fetal lung tissue GW18; Xenium (GW 18)
human lung 8.6 GB 980,410 cells 339 genes silver NCBI GEO policy
TechnologyXenium
Organismhuman
Tissuelung
Size8.6 GB
Cells980,410
Genes339
silver NCBI GEO policy Open in Vitessce

Cite this collection

doi.org/10.1038/s41467-024-50281-5 ↗
BibTeX
@article{Quach_2024,
  title = {Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticity},
  volume = {15},
  ISSN = {2041-1723},
  url = {http://dx.doi.org/10.1038/s41467-024-50281-5},
  DOI = {10.1038/s41467-024-50281-5},
  number = {1},
  journal = {Nature Communications},
  publisher = {Springer Science and Business Media LLC},
  author = {Quach, Henry and Farrell, Spencer and Wu, Ming Jia Michael and Kanagarajah, Kayshani and Leung, Joseph Wai-Hin and Xu, Xiaoqiao and Kallurkar, Prajkta and Turinsky, Andrei L. and Bear, Christine E. and Ratjen, Felix and Kalish, Brian and Goyal, Sidhartha and Moraes, Theo J. and Wong, Amy P.},
  year = {2024},
  month = July
}