Cell-in-drop genotyping detects megabase-scale loss of heterozygosity as a quantitative marker for CRISPR-Cas9 on-target toxicity
Darpan Medhi, Linas Mazutis, Maria Jasin
bioRxiv · Nov 2, 2026 · PreprintBioengineering
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Memorial Sloan Kettering Cancer CenterORCID 0000-0002-5552-6427Unclaimed ORCID profile · follow to get notified of new preprints
14 papers
Recent·Most cited
Darpan Medhi, Linas Mazutis, Maria Jasin
bioRxiv · Nov 2, 2026 · PreprintBioengineering
Christopher Beltz, Zekai Qiu, Leon Sadowski, Joscha A. Kraske, Anmol Aggarwal, Àlvaro Quintanal-Villalonga, Parvathy Manoj, Andrea Littbarski, Sunanjay Bajaj, Brigita Meškauskaitė, Shigeaki Umeda, Linas Mažutis, Samuel A. Rose, Joseph M. Chan, Tal Nawy, , Thomas Walle
The paper introduces Suco and Compocyte to classify immune cells from 3,965 patients, identifying new macrophage and monocyte states and T cell memory erosion in metastases.
bioRxiv · Jun 21, 2026 · PreprintBioinformatics
Denis Baronas, Justina Žvirblytė, Simonas Norvaisis, Greta Leonavičienė, Karolis Goda, Vincenta Mikulenaite, Vytautas Kašėta, Karolis Šablauskas, Laimonas Griškevičius, Simonas Juzėnas, Linas Mažutis
This paper introduces a semi-permeable capsule technology for high-throughput single-cell -omics, demonstrating its utility in scRNA-Seq of hematopoietic disorders and uncovering transcriptome changes in AML.
Science · Dec 18, 2025Peer-reviewedGenomics
Alejandro Jiménez-Sánchez, Sitara Persad, Akimasa Hayashi, Shigeaki Umeda, Roshan Sharma, Yubin Xie, Arnav Mehta, Wungki Park, Ignas Masilionis, Tinyi Chu, Feiyang Zhu, Jungeui Hong, Ronan Chaligné, Eileen Mary O'Reilly, Linas Mažutis, , Dana Pe’er
The paper analyzes transcriptomic changes in metastatic pancreatic cancer using a patient's autopsy data to identify site-specific gene programs and clonal phylogeny.
Cancer Research · Dec 11, 2025Peer-reviewedBioinformatics
Catherine K. Xu, Georg Meisl, Nikita Moshkov, Niklas Arndt Schmacke, Karolis Goda, Alexey Shkarin, Maximilian F Schlögel, Sandra Diebold, Christine Schweitzer, Arif B. Ekici, Tuomas P. J. Knowles, Fabian Joachim Theis, Linas Mažutis, Jochen R. Guck
The paper introduces a method to link single-cell imaging and gene expression data through multimodal droplet barcoding, identifying genes correlated with phenotypic features.
bioRxiv · Sep 1, 2025 · PreprintGenomics
Achille Nazaret, Joy Linyue Fan, Vincent‐Philippe Lavallée, Cassandra Burdziak, Andrew E. Cornish, Vaidotas Kiseliovas, Robert L. Bowman, Ignas Masilionis, Jaeyoung Chun, Shira Esther Eisman, James Wang, Justin Hong, Lingting Shi, Ross L. Levine, Linas Mažutis, , Elham Azizi
Decipher is a deep generative model that integrates single-cell RNA-seq data to visualize and characterize transitions between normal and perturbed cell states across different diseases.
Genome biology · Jul 23, 2025Peer-reviewedBioinformatics
Hadrien Gourlé, Iryna Yakovenko, Jyoti Verma, Julian Dicken, Florian Albrecht, Arthur Stenlund, Chetan Sharaf, Chinmay Kumar Dwibedi, Linas Mažutis, Johan Normark, Nongfei Sheng, Nicklas Strömberg, Tommy Löfstedt, Laura M. Carroll, Johan Henriksson
This paper introduces Bascet and Zorn, tools for scalable single-cell metagenomic analysis, demonstrating their utility on mock and human saliva samples.
bioRxiv · Jun 20, 2025 · PreprintMicrobiology
Simonas Juzėnas, Karolis Goda, Vaidotas Kiseliovas, Justina Žvirblytė, Àlvaro Quintanal-Villalonga, Juozas Siurkus, Juozas Nainys, Linas Mažutis
The paper introduces inDrops-2, a cost-efficient scRNA-seq platform that profiles clinical samples with sensitivity comparable to commercial systems and demonstrates its utility in analyzing lung carcinoma samples.
Nucleic Acids Research · Dec 26, 2024Peer-reviewedMolecular Biology
Samir Zaidi, Jooyoung Park, Joseph Minhow Chan, Martine P. Roudier, Jimmy L. Zhao, Anuradha Gopalan, Kristine M. Wadosky, Radhika A. Patel, Erolcan Sayar, Wouter R. Karthaus, D. Henry Kates, Ojasvi Chaudhary, Tianhao Xu, Ignas Masilionis, Linas Mažutis, , Charles L. Sawyers
The paper uses single-cell analysis to study how cell surface antigen expression changes in treatment-resistant prostate cancer, revealing transcriptional heterogeneity and shared gene regulatory networks between NEPC and SCLC.
Proceedings of the National Academy of Sciences · Jul 5, 2024Peer-reviewedCancer Biology
Greta Leonavičienė, Linas Mažutis
This paper introduces a high-throughput RNA cytometry method using semi-permeable microcapsules to enable digital profiling of single-cell gene expression.
Nucleic Acids Research · Oct 7, 2022Peer-reviewedMolecular Biology
Yuri Pritykin, Joris van der Veeken, Allison R. Pine, Yi Zhong, Merve Şahin, Linas Mažutis, Dana Pe’er, Alexander Yu Rudensky, Christina S. Leslie
The paper defines a shared differentiation trajectory of CD8 T cell dysfunction across cancer and infection using ATAC-seq and RNA-seq data from multiple studies.
Molecular Cell · Apr 22, 2021Peer-reviewedGenomics
Faten A. Sayed, Lay Kodama, Joe C. Udeochu, Li Fan, Gillian Carling, David Le, Qingyun Li, Lu Zhou, Hansruedi Mathys, Minghui Wang, Xiang Niu, Linas Mažutis, Xueqiao Jiang, Xueting Wang, Man Ying Wong, , Li Gan
This study identifies R47H-TREM2 mutation-induced proinflammatory microglial states in human AD and tauopathy mice, showing Akt pathway involvement and potential therapeutic targets.
bioRxiv · Jul 24, 2020 · PreprintNeuroscience
Manu N. Setty, Vaidotas Kiseliovas, Jacob Levine, Adam Gayoso, Linas Mažutis, Dana Pe’er
Palantir models cell fate as a probabilistic process using entropy to analyze differentiation trajectories in human hematopoiesis, identifying key transcription factors and terminal states.
Nature Biotechnology · Mar 21, 2019Peer-reviewedSystems Biology
David van Dijk, Roshan Sharma, Juozas Nainys, Kristina Yim, Pooja Kathail, Ambrose Carr, Cassandra Burdziak, Kevin R. Moon, Christine Louise Chaffer, Diwakar Ram Pattabiraman, Brian Bierie, Linas Mažutis, Guy Wolf, Smita Krishnaswamy, Dana Pe’er
MAGIC improves single-cell RNA-seq data by imputing missing values and revealing gene-gene interactions through a diffusion-based method.
Cell · Jan 1, 2018Peer-reviewedBioinformatics