sciCAN: single-cell chromatin accessibility and gene expression data integration via cycle-consistent adversarial network.

sciCAN: single-cell chromatin accessibility and gene expression data integration via cycle-consistent adversarial network.
复制标题

DOI:
10.1038/s41540-022-00245-6
复制
发表时间:
2022-09-12
影响因子:
4
通讯作者:
--
中科院分区:
生物学2区
文献类型:
--
作者:

文献摘要

参考文献

相似文献

单细胞技术的繁荣带来了来自不同来源的高维数据的激增,这些数据从不同的角度代表了蜂窝系统。随着这些单细胞技术的进步,跨模式整合单细胞数据成为一个新的计算挑战。在这里,我们提出了一种对抗性的方法,sciCAN,以无监督的方式整合单细胞染色质可及性和基因表达数据。我们在5个scATAC-seq/scRNA-seq数据集中用5种现有方法对sciCAN进行了基准测试,证明了我们的方法处理数据集成时,在数据集之间具有一致的性能,并且比其他5种现有方法更好地平衡了模态之间的相互传输。我们进一步将sciCAN应用于10 X Multiome数据,并证实了集成表示保留了造血层次内的生物学关系。最后,我们研究了CRISPR干扰的单细胞K562 ATAC-seq和RNA-seq数据,以识别对这些不同模式的不同干扰具有相关响应的细胞。
The boom in single-cell technologies has brought a surge of high dimensional data that come from different sources and represent cellular systems from different views. With advances in these single-cell technologies, integrating single-cell data across modalities arises as a new computational challenge. Here, we present an adversarial approach, sciCAN, to integrate single-cell chromatin accessibility and gene expression data in an unsupervised manner. We benchmarked sciCAN with 5 existing methods in 5 scATAC-seq/scRNA-seq datasets, and we demonstrated that our method dealt with data integration with consistent performance across datasets and better balance of mutual transferring between modalities than the other 5 existing methods. We further applied sciCAN to 10X Multiome data and confirmed that the integrated representation preserves biological relationships within the hematopoietic hierarchy. Finally, we investigated CRISPR-perturbed single-cell K562 ATAC-seq and RNA-seq data to identify cells with related responses to different perturbations in these different modalities.
DOI: 10.1038/nbt.4314
发表时间: 2019-01-01
影响因子: 46.9
作者:
Becht, Etienne;McInnes, Leland;Newell, Evan W.
通讯作者: Newell, Evan W.
DOI: 10.1038/s41587-021-01161-6
发表时间: 2022-05
影响因子: 46.9
作者:
Lin, Yingxin;Wu, Tung-Yu;Wan, Sheng;Yang, Jean Y. H.;Wong, Wing H.;Wang, Y. X. Rachel
通讯作者: Wang, Y. X. Rachel
DOI: 10.1038/ng.3646
发表时间: 2016-10
期刊: NATURE GENETICS
影响因子: 30.8
作者:
Corces, M. Ryan;Buenrostro, Jason D.;Wu, Beijing;Greenside, Peyton G.;Chan, Steven M.;Koenig, Julie L.;Snyder, Michael P.;Pritchard, Jonathan K.;Kundaje, Anshul;Gkeenleaf, William J.;Majeti, Ravindra;Chang, Howard Y.
通讯作者: Chang, Howard Y.
DOI: 10.1016/j.cell.2016.11.038
发表时间: 2016-12-15
期刊: CELL
影响因子: 64.5
作者:
Dixit, Atray;Pamas, Oren;Li, Biyu;Chen, Jenny;Fulco, Charles P.;Jerby-Amon, Livnat;Marjanovic, Nemanja D.;Dionne, Danielle;Burks, Tyler;Raychowdhury, Raktima;Adamson, Britt;Norman, Thomas M.;Lander, Eric S.;Weissman, Jonathan S.;Friedman, Nir;Regev, Aviv
通讯作者: Regev, Aviv
DOI: 10.1038/s41586-018-0414-6
发表时间: 2018-08
期刊: Nature
影响因子: 64.8
作者:
La Manno G;Soldatov R;Zeisel A;Braun E;Hochgerner H;Petukhov V;Lidschreiber K;Kastriti ME;Lönnerberg P;Furlan A;Fan J;Borm LE;Liu Z;van Bruggen D;Guo J;He X;Barker R;Sundström E;Castelo-Branco G;Cramer P;Adameyko I;Linnarsson S;Kharchenko PV
通讯作者: Kharchenko PV