CUT&RUNTools 2.0: a pipeline for single-cell and bulk-level CUT&RUN and CUT&Tag data analysis

Author:

Yu Fulong1234,Sankaran Vijay G1234ORCID,Yuan Guo-Cheng1235ORCID

Affiliation:

1. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA

2. Division of Hematology/Oncology, Boston Children’s Hospital, Boston, MA 02115, USA

3. Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA

4. Program in Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02115, USA

5. Department of Genetics and Genomic Sciences, Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA

Abstract

Abstract Motivation Genome-wide profiling of transcription factor binding and chromatin states is a widely-used approach for mechanistic understanding of gene regulation. Recent technology development has enabled such profiling at single-cell resolution. However, an end-to-end computational pipeline for analyzing such data is still lacking. Results Here, we have developed a flexible pipeline for analysis and visualization of single-cell CUT&Tag and CUT&RUN data, which provides functions for sequence alignment, quality control, dimensionality reduction, cell clustering, data aggregation and visualization. Furthermore, it is also seamlessly integrated with the functions in original CUT&RUNTools for population-level analyses. As such, this provides a valuable toolbox for the community. Availability and implementation https://github.com/fl-yu/CUT-RUNTools-2.0. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

NIH

New York Stem Cell Foundation and NIH

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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