BISCUIT: an efficient, standards-compliant tool suite for simultaneous genetic and epigenetic inference in bulk and single-cell studies

Author:

Zhou Wanding1ORCID,Johnson Benjamin K1ORCID,Morrison Jacob1ORCID,Beddows Ian1,Eapen James1,Katsman Efrat2,Semwal Ayush1,Habib Walid Abi1,Heo Lyong1,Laird Peter W1ORCID,Berman Benjamin P2ORCID,Triche Timothy J1ORCID,Shen Hui1ORCID

Affiliation:

1. Department of Epigenetics, Van Andel Institute , Grand Rapids , MI  49503 , USA

2. Department of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem , Jerusalem  9112102 , Israel

Abstract

Abstract Data from both bulk and single-cell whole-genome DNA methylation experiments are under-utilized in many ways. This is attributable to inefficient mapping of methylation sequencing reads, routinely discarded genetic information, and neglected read-level epigenetic and genetic linkage information. We introduce the BISulfite-seq Command line User Interface Toolkit (BISCUIT) and its companion R/Bioconductor package, biscuiteer, for simultaneous extraction of genetic and epigenetic information from bulk and single-cell DNA methylation sequencing. BISCUIT’s performance, flexibility and standards-compliant output allow large, complex experimental designs to be characterized on clinical timescales. BISCUIT is particularly suited for processing data from single-cell DNA methylation assays, with its excellent scalability, efficiency, and ability to greatly enhance mappability, a key challenge for single-cell studies. We also introduce the epiBED format for single-molecule analysis of coupled epigenetic and genetic information, facilitating the study of cellular and tissue heterogeneity from DNA methylation sequencing.

Funder

National Institutes of Health

Michelle Lunn Hope Foundation

Grand Rapids Community Foundation

Van Andel Institute Department of Epigenetics

Publisher

Oxford University Press (OUP)

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