Document Type
Article
Publication Date
9-1-2021
Publication Title
Genome biology
Keywords
JGM
JAX Source
Genome Biol 2021 Sep 1; 22(1):252
Volume
22
Issue
1
First Page
252
Last Page
252
ISSN
1474-760X
PMID
34465366
DOI
https://doi.org/10.1186/s13059-021-02469-x
Grant
GM124922, AG052608, Department of Defense award number W81XWH-18-0401, American Diabetes Association Pathway to Stop Diabetes Accelerator Award
Abstract
Detecting multiplets in single nucleus (sn)ATAC-seq data is challenging due to data sparsity and limited dynamic range. AMULET (ATAC-seq MULtiplet Estimation Tool) enumerates regions with greater than two uniquely aligned reads across the genome to effectively detect multiplets. We evaluate the method by generating snATAC-seq data in the human blood and pancreatic islet samples. AMULET has high precision, estimated via donor-based multiplexing, and high recall, estimated via simulated multiplets, compared to alternatives and identifies multiplets most effectively when a certain read depth of 25K median valid reads per nucleus is achieved.
Recommended Citation
Thibodeau A,
Eroglu A,
McGinnis C,
Lawlor N,
Nehar-Belaid D,
Kursawe R,
Marches R,
Conrad D,
Kuchel G,
Gartner Z,
Banchereau J,
Stitzel ML,
Cicek A,
Ucar D.
AMULET: a novel read count-based method for effective multiplet detection from single nucleus ATAC-seq data. Genome Biol 2021 Sep 1; 22(1):252
Comments
We thank the Beck and Lee labs for their feedback and suggestions on how to handle repetitive element sequences within our software. We thank Jane Cha for her help with enhancing schematic figures for this project. We thank Ucar/Stitzel lab members for their constructive feedback. We thank Dr. Motakis for help with naming our software. Finally,we thank the Jackson Laboratory Single Cell and Genome Technologies cores for generating snATAC-seq data.
This article is licensed under a Creative Commons Attribution 4.0 International License.