simATAC: A single-cell ATAC-seq simulation framework
Zeinab Navidi, Lin Zhang, Bo Wang
simATAC generates synthetic scATAC-seq datasets with known cell labels to benchmark analytical pipelines.
Genome biology · Mar 4, 2021Peer-reviewedBioinformatics
786 papers
Zeinab Navidi, Lin Zhang, Bo Wang
simATAC generates synthetic scATAC-seq datasets with known cell labels to benchmark analytical pipelines.
Genome biology · Mar 4, 2021Peer-reviewedBioinformatics
Jimmy Tsz Hang Lee, Nikolaos Patikas, Vladimir Yu Kiselev, Martin Hemberg
scfind enables efficient querying of single-cell data to evaluate marker genes, perform in silico gating, and support multi-omics analyses.
Nature Methods · Mar 1, 2021Peer-reviewedBioinformatics
Rongxin Fang, Sebastian Preißl, Yang Li, Xiaomeng Hou, Jacinta D. Lucero, Xinxin Wang, Amir Motamedi, Andrew K. Shiau, Xinzhu Zhou, Fangming Xie, Eran A. Mukamel, Kai Zhang, Yanxiao Zhang, M. Margarita Behrens, Joseph R. Ecker, Bing Ren
SnapATAC is a software package for analyzing scATAC-seq data, revealing regulatory elements and transcriptional regulators in mouse brain cells.
Nature Communications · Feb 26, 2021Peer-reviewedBioinformatics
Jeffrey M. Granja, M. Ryan Corces, Sarah E. Pierce, S. Tansu Bagdatli, Hani Choudhry, Howard Y. Chang, William James Greenleaf
ArchR, an HDF5-backed R suite for end-to-end scATAC-seq analysis, outpaces SnapATAC and Signac and processes over 1.2 million simulated cells within 8 h on a laptop.
Nature Genetics · Feb 25, 2021Peer-reviewedGenomics✦ In-depth digest
Casey A. Thornton, Ryan M. Mulqueen, Kristof A. Torkenczy, Andrew Nishida, Eve G. Lowenstein, Andrew J. Fields, Frank J. Steemers, Wenri H. Zhang, Heather L. McConnell, Randy L Woltjer, Anusha Mishra, Kevin M. Wright, Andrew Adey
The paper introduces sciMAP-ATAC, a method for spatially resolved single-cell chromatin accessibility profiling, and applies it to study cortical lamination, spatial trajectories, and ischemic infarct progression in mouse and human tissues.
Nature Communications · Feb 24, 2021Peer-reviewedGenetics
S. Taavitsainen, N. Engedal, S. Cao, F. Handle, A. Erickson, S. Prekovic, D. Wetterskog, T. Tolonen, E. M. Vuorinen, A. Kiviaho, R. Nätkin, T. Häkkinen, W. Devlies, S. Henttinen, R. Kaarijärvi, , A. Urbanucci
The paper uses single-cell ATAC and RNA sequencing to identify pre-existing and treatment-persistent stem-like cell subpopulations in prostate cancer models that predict treatment response.
bioRxiv · Feb 9, 2021Cancer Biology
Zhanlin Chen, Jing Zhang, Jason J. Liu, Zixuan Zhang, Jiangqi Zhu, Donghoon Lee, Min Xu, Mark Gerstein
SCAN-ATAC-Sim simulates scATAC-seq data from bulk ATAC-seq to benchmark analysis methods with known cell-type labels.
Bioinformatics · Jan 14, 2021Peer-reviewedBioinformatics
Tri Le, Tan Phan, Minh Pham, Dat Tran, Loc Lam, Ngoc Tung Nguyen, Thao Truong, Hy Vuong, Tam Luu, Nam Phung, Ngan Pham, Trang Thi Thu Nguyen, Oanh Minh Pham, An Nguyen, Huy Tan Nguyen, , Son Truong Pham
A downloadable application pairs a curated single-cell database with a big-data analytics layer and a visualisation module for exploring single-cell omics data.
bioRxiv · Dec 11, 2020 · PreprintBioinformatics
Jinzhuang Dou, Shaoheng Liang, Vakul Mohanty, Xuesen Cheng, Sangbae Kim, Jongsu Choi, Yumei Li, Katayoun Rezvani, Rui Chen, Ken Chen
bindSC integrates single-cell multi-omics data accurately by aligning rows and columns without approximations, outperforming existing methods in various biological contexts.
bioRxiv · Dec 11, 2020 · PreprintBioinformatics
C. Chen, W. Yu, F. Alikarami, Q. Qiu, C.-h. Chen, J. Flournoy, P. Gao, Y. Uzun, L. Fang, Y. Yu, Q. Zhu, K. Wang, C. Libbrecht, A. Felmeister, I. Rozich, , K. Tan
This study uses single-cell multi-omics to identify lineage plasticity and stem-cell-like blasts in KMT2A-rearranged leukemia, linking these features to poor prognosis in infants.
bioRxiv · Dec 6, 2020 · PreprintCancer Biology
Paola Benaglio, Jacklyn M. Newsome, Jee Yun Han, Joshua Chiou, Anthony Aylward, Sierra Corban, Mei-Lin Okino, Jaspreet Kaur, David U. Gorkin, Kyle J. Gaulton
The paper uses snATAC-seq to map chromatin accessibility QTLs in immune cell types and fine-maps complex trait loci, identifying cell type-specific causal variants.
bioRxiv · Dec 3, 2020 · PreprintGenomics
Rachesh Sharma, Neetesh Pandey, Aanchal Mongia, Shreya V. Mishra, Angshul Majumdar, Vibhor Kumar
FITs recovers true signals from sparse and noisy single-cell open-chromatin profiles by using a forest of imputation trees to avoid bias and preserve cell-type-specific activity.
NAR Genomics and Bioinformatics · Nov 19, 2020Peer-reviewedBioinformatics
Pacôme Prompsy, Pia Kirchmeier, Justine Marsolier, Marc Deloger, Nicolas Servant, Céline Vallot
ChromSCape is an R/Shiny tool for analyzing single-cell chromatin data, enabling subpopulation identification and differential region analysis in epigenomic studies.
Nature Communications · Nov 11, 2020Peer-reviewedBioinformatics
Zhenyi Wang, Yanjie Zhong, Zhaofeng Ye, Lang Zeng, Yang Chen, Minglei Shi, Minping Qian, Michael Q. Zhang
MarkovHC is a clustering algorithm that identifies cell types, trajectories, and critical points in single-cell omics data by reconstructing a pseudo-energy landscape based on metastability theory.
bioRxiv · Nov 4, 2020 · PreprintBioinformatics
Pengcheng Zeng, Jiaxuan Wangwu, Zhixiang Lin
This paper introduces a coupled co-clustering-based transfer learning method for integrating multimodal single-cell genomic data, improving clustering performance and matching cell subpopulations across data types.
Briefings in Bioinformatics · Oct 30, 2020Peer-reviewedBioinformatics
M. Ryan Corces, Anna Shcherbina, Soumya Kundu, Michael J. Gloudemans, Laure Frésard, Jeffrey M. Granja, Bryan H. Louie, Tiffany Y. Eulalio, Shadi Shams, S. Tansu Bagdatli, Maxwell R. Mumbach, Boxiang Liu, Kathleen S. Montine, William James Greenleaf, Anshul Bharat Kundaje, , Thomas Jude Montine
The paper uses single-cell epigenomic data to identify functional SNPs associated with Alzheimer's and Parkinson's disease, revealing novel gene-disease associations and regulatory mechanisms.
Nature Genetics · Oct 26, 2020Peer-reviewedGenomics
J. Liao, H. C. Suen, A. C. S. Luk, A. W. T. Lee, J. K. W. Ng, T. H. T. Chan, M. Y. Cheung, D. Y. L. Chan, H. Qi, W.-Y. Chan, R. M. Hobbs, T. L. Lee
The paper uses scATAC-seq to identify epigenetic heterogeneity in male germline stem cells associated with an EMT-like process and shows G9a regulates this process.
bioRxiv · Oct 12, 2020 · PreprintCell Biology
Jialin Liu, Chao Gao, Joshua Sodicoff, Velina Kozareva, Evan Z. Macosko, Joshua D. Welch
The paper provides a protocol for using LIGER to jointly define cell types from multiple single-cell datasets, including RNA-seq and ATAC-seq data.
Nature Protocols · Oct 12, 2020Peer-reviewedBioinformatics
Evgenij Fiškin, Caleb A. Lareau, Gökçen Eraslan, Leif S. Ludwig, Aviv Regev
The paper introduces PHAGE-ATAC, a method for simultaneous single-cell measurement of surface proteins, chromatin accessibility, and mtDNA-based clonal tracing, and demonstrates its application in human immune cells.
bioRxiv · Oct 1, 2020 · PreprintGenomics
Ritambhara Singh, Pınar Demetçi, Giancarlo Bonora, Vijay Ramani, Choli Lee, He Fang, Zhijun Duan, Xinxian Deng, Jay Shendure, Christine M. Distèche, William Stafford Noble
This paper applies and extends MMD-MA to align single-cell transcriptome and chromatin accessibility data from ~2000 cells, demonstrating its scalability and accuracy.
ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics (ACM-BCB) · Sep 21, 2020Peer-reviewedBioinformatics
E. F. Semeraro, L. Marx, J. Mandl, M. Frewein, H. Scott, S. Prevost, H. Bergler, K. Lohner, G. Pabst
The paper revises a scattering model for live E. coli to better fit experimental data and reveals structural differences between strains.
bioRxiv · Sep 18, 2020Biophysics
Qiao Rui Xing, Chadi A. El Farran, Pradeep Gautam, Yu Song Chuah, Tushar Warrier, Chi-Hang Toh, Nam-Young Kang, Shigeki Sugii, Young‐Tae Chang, Jian Xu, James J. Collins, George Q. Daley, Hu Li, Li‐Feng Zhang, Yuin‐Han Loh
This study uses scRNA-Seq and scATAC-Seq to show that human reprogramming occurs through asynchronous, diverse trajectories with distinct regulatory networks.
Science Advances · Sep 11, 2020Peer-reviewedGenomics
Eleni P. Mimitou, Caleb A. Lareau, Kelvin Y. Chen, André Luiz Zorzetto-Fernandes, Yusuke Takeshima, Wendy Luo, Tse-Shun Huang, Bertrand Z. Yeung, Pratiksha I. Thakore, James B. Wing, Kristopher L. Nazor, Shimon Sakaguchi, Leif S. Ludwig, Vijay G. Sankaran, Aviv Regev, Peter Smibert
This paper introduces ASAP-seq, a method to simultaneously profile chromatin accessibility, protein levels, and mtDNA in single cells, demonstrating its application in hematopoietic differentiation and T cell perturbations.
bioRxiv · Sep 8, 2020 · PreprintGenomics
E. Swanson, C. Lord, J. Reading, A. T. Heubeck, A. K. Savage, R. Green, X.-j. Li, T. R. Torgerson, T. F. Bumol, L. T. Graybuck, P. J. Skene
The paper introduces TEA-seq, a trimodal assay that integrates scRNA-seq, cell surface epitopes, and scATAC-seq to improve single-cell analysis of transcription, epitopes, and chromatin accessibility.
bioRxiv · Sep 4, 2020 · PreprintImmunology
Steven J. Wu, Scott N. Furlan, Anca B. Mihalas, Hatice S Kaya-Okur, Abdullah Hamid Feroze, Samuel Emerson, Ye Zheng, Kalee Carson, Patrick Joseph Cimino, Christopher Dirk Keene, Jay F. Sarthy, Raphaël Gottardo, Kami Ahmad, Steven Henikoff, Anoop P. Patel
This paper develops scCUT&Tag to profile H3K27me3 in single cells, distinguishing cell types in blood and identifying PcG activity changes in brain tumors before and after treatment.
bioRxiv · Sep 4, 2020 · PreprintGenomics
Qiao Liu, Shengquan Chen, Rui Jiang, Wing Hung Wong
scDEC uses deep generative networks to simultaneously model and cluster scATAC-seq data, showing better performance than existing tools and enabling trajectory inference and cell type discovery.
bioRxiv · Aug 17, 2020 · PreprintBioinformatics
A. J. Quenum, M. Cloutier, M. A. Santharam, M. Mayhue, S. Ramanathan, S. Ilangumaran
This study shows cytokine priming of naive CD8+ T cells changes chromatin accessibility, with some overlaps seen with antigen stimulation, suggesting a poised state for enhanced TCR responsiveness.
bioRxiv · Aug 11, 2020 · PreprintImmunology
Florian Noack, Silvia Vangelisti, Madalena Carido, Faye Chong, Boyan Bonev
The paper uses multiomics data to map regulatory changes in the mouse neocortex during development, identifying novel enhancer-gene pairs and epigenetic remodeling patterns.
bioRxiv · Aug 7, 2020 · PreprintGenomics
A. Farmer, S. Thibivilliers, K. H. Ryu, J. Schiefelbein, M. Libault
The paper uses sNucRNA-seq and sNucATAC-seq to study chromatin remodeling's impact on gene expression in Arabidopsis root nuclei, revealing cell-type-specific chromatin accessibility patterns.
bioRxiv · Jul 27, 2020 · PreprintPlant Biology
Mandy Meijer, Eneritz Agirre, Mukund Kabbe, Cassandra A. van Tuijn, Abeer Heskol, Ana Mendanha Falcão, M. Ryan Corces, Thomas Jude Montine, Xingqi Chen, Howard Y. Chang, Gonçalo Castelo‐Branco
This study identifies a primed chromatin state in oligodendroglia that facilitates rapid activation of immune gene programs in multiple sclerosis.
bioRxiv · Jul 21, 2020 · PreprintNeuroscience