TY - JOUR
T1 - SMAC: identifying DNA N6-methyladenine (6mA) at the single-molecule level using SMRT CCS data
AU - Li, Haicheng
AU - Niu, Junhua
AU - Sheng, Yalan
AU - Liu, Yifan
AU - Gao, Shan
N1 - This work was supported by the National Natural Science Foundation of China (32125006 to S.G.), Natural Science Foundation of Shandong Province of China (ZR2024ZD40 to S.G.), the Science & Technology Innovation Project of Laoshan Laboratory (LSKJ202203203 to S.G.), and the National Science Foundation (MCB-2435178 to Y.L.).
© The Author(s) 2025. Published by Oxford University Press.
PY - 2025/3
Y1 - 2025/3
N2 - DNA modifications, such as N6-methyladenine (6mA), play important roles in various processes in eukaryotes. Single-molecule, real-time (SMRT) sequencing enables the direct detection of DNA modifications without requiring special sample preparation. However, most SMRT-based studies of 6mA rely on ensemble-level consensus by combining multiple reads covering the same genomic position, which misses the single-molecule heterogeneity. While recent methods have aimed at single-molecule level detection of 6mA, limitations in sequencing platforms, resolution, accuracy, and usability restrict their application in comprehensive epigenetic studies. Here, we present SMAC (single-molecule 6mA analysis of CCS reads), a novel framework for accurately detecting 6mA at the single-molecule level using SMRT circular consensus sequencing (CCS) data from the Sequel II system. It is an automated method that streamlines the entire workflow by packaging both existing softwares and built-in scripts, with user-defined parameters to allow easy adaptation for various studies. By utilizing the statistical distribution characteristics of enzyme kinetic indicators on single DNA molecules rather than a fixed cutoff, SMAC significantly improves 6mA detection accuracy at the single-nucleotide and single-molecule levels. It simplifies analysis by providing comprehensive information, including quality control, statistical analysis, and site visualization, directly from raw sequencing data. SMAC is a powerful new tool that enables de novo detection of 6mA and empowers investigation of its functions in modulating physiological processes.
AB - DNA modifications, such as N6-methyladenine (6mA), play important roles in various processes in eukaryotes. Single-molecule, real-time (SMRT) sequencing enables the direct detection of DNA modifications without requiring special sample preparation. However, most SMRT-based studies of 6mA rely on ensemble-level consensus by combining multiple reads covering the same genomic position, which misses the single-molecule heterogeneity. While recent methods have aimed at single-molecule level detection of 6mA, limitations in sequencing platforms, resolution, accuracy, and usability restrict their application in comprehensive epigenetic studies. Here, we present SMAC (single-molecule 6mA analysis of CCS reads), a novel framework for accurately detecting 6mA at the single-molecule level using SMRT circular consensus sequencing (CCS) data from the Sequel II system. It is an automated method that streamlines the entire workflow by packaging both existing softwares and built-in scripts, with user-defined parameters to allow easy adaptation for various studies. By utilizing the statistical distribution characteristics of enzyme kinetic indicators on single DNA molecules rather than a fixed cutoff, SMAC significantly improves 6mA detection accuracy at the single-nucleotide and single-molecule levels. It simplifies analysis by providing comprehensive information, including quality control, statistical analysis, and site visualization, directly from raw sequencing data. SMAC is a powerful new tool that enables de novo detection of 6mA and empowers investigation of its functions in modulating physiological processes.
KW - DNA N-methyladenine (6mA)
KW - single molecule
KW - SMAC (single-molecule 6mA analysis of CCS reads)
KW - SMRT CCS sequencing
UR - http://www.scopus.com/inward/record.url?scp=105002685665&partnerID=8YFLogxK
U2 - 10.1093/bib/bbaf153
DO - 10.1093/bib/bbaf153
M3 - Journal article
C2 - 40205850
AN - SCOPUS:105002685665
SN - 1467-5463
VL - 26
JO - Briefings in Bioinformatics
JF - Briefings in Bioinformatics
IS - 2
M1 - bbaf153
ER -