Skip to content
DraconiticResearch
Search Sources API
190,860 studies31 sourcesUpdated 33 min ago
PreprintCC BYbioRxiv

Atlas-scale single-cell analysis beyond in-memory paradigm with scAtlasPy

  1. 1XIDIAN UNIVERSITY

Abstract

Single-cell atlases are rapidly outgrowing the memory capacity of standard workstations, challenging the in-memory paradigm underlying mainstream computational ecosystems. Here, scAtlasPy decouples scale of atlas from memory capacity by leveraging the disk-resident computing. It enables full-resolution analysis of a 100-million-cell atlas with only 42.9 GB peak memory, whereas state-of-the-art platforms are limited at 3 million cells with 512 GB memory. scAtlasPy achieves 137,745 cells/s, 10.4x faster than scDataset with 82.6% lower memory usage for random minibatch retrieval. Its extensible architecture offers a flexible platform for diverse atlas-scale analytical tasks, facilitating the discovery of complex cellular heterogeneity and functions in massive cell atlases.

Related

  1. Beyond the Single Pathogen Paradigm in Citrus: A Pathobiome Perspective on Disease Complexes, Microbiome Dysbiosis, and Management
    Min Luo, Hongyu Zhang, Ting Zhong +5
    Plants (Basel, Switzerland)Peer-reviewedCC BYFull textPlant biologyEurope PMC
  2. Emotional Processing in a Nap Paradigm: The Role of Sleep Stages in Memory and Reactivity
    Costanza Colombo, Angie Baldassarri, Umberto Granziol +5
    PsychophysiologyPeer-reviewedCC BYFull textNeuroscienceEurope PMC
  3. Astrocytes and memory: emerging evidence and a paradigm shift
    Sen Zhang, Qinglu Wang
    Cell Communication and Signaling : CCSPeer-reviewedCC BY-NC-ND 4.0Full text1 citedNeurosciencePMC
  4. Virtual Silcton and Beyond: A Virtual Environment Paradigm Framework for Spatial Navigation Research
    Steven Weisberg, Victor Schinazi
    PsyArXivPreprintCC BY 4.0Full textNeuroscienceOSF
  5. Cell identity competes with surface tension to determine stromal organization in tumor spheroids beyond the CAF shell paradigm.
    Claire Wilhelm
    Proceedings of the National Academy of Sciences of the United States of AmericaPeer-reviewedCC BYFull textCell biologyEurope PMC
BibTeX
@misc{xu2026atlasscale,
  title = {{Atlas-scale single-cell analysis beyond in-memory paradigm with scAtlasPy}},
  author = {H. Xu and Y. Ye and S. Zhang and R. Xie and J. Li and J. Lin and Y. Hu and L. Gao},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.03.748766},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.03.748766v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Atlas-scale single-cell analysis beyond in-memory paradigm with scAtlasPy
AU  - H. Xu
AU  - Y. Ye
AU  - S. Zhang
AU  - R. Xie
AU  - J. Li
AU  - J. Lin
AU  - Y. Hu
AU  - L. Gao
PY  - 2026
DA  - 2026/09/03
PB  - bioRxiv
DO  - 10.64898/2026.09.03.748766
UR  - https://www.biorxiv.org/content/10.64898/2026.09.03.748766v1
AB  - Single-cell atlases are rapidly outgrowing the memory capacity of standard workstations, challenging the in-memory paradigm underlying mainstream computational ecosystems. Here, scAtlasPy decouples scale of atlas from memory capacity by leveraging the disk-resident computing. It enables full-resolution analysis of a 100-million-cell atlas with only 42.9 GB peak memory, whereas state-of-the-art platforms are limited at 3 million cells with 512 GB memory. scAtlasPy achieves 137,745 cells/s, 10.4x faster than scDataset with 82.6% lower memory usage for random minibatch retrieval. Its extensible architecture offers a flexible platform for diverse atlas-scale analytical tasks, facilitating the discovery of complex cellular heterogeneity and functions in massive cell atlases.
ER  -