Author:
Wang Ke,Song Mengmeng,Li Min,Cui Tianyu,Liu Zhentian,Yu Enjie,Fang Huan,Gao Xuan,Xia Xuefeng,Wang Jiayin,Guan Yanfang,Liu Tao,Yi Xin
Abstract
AbstractHigh-throughput UMI technology sequencing is widely used in early tumor screening, detection, recurrence monitoring, etc. Detecting extremely low-frequency mutations is especially important for monitoring tumor recurrence, so high-precision data, as well as high-quality data, are required. We developedRealSeq2, a new integrated data-preprocessing software based on fastp and gencore, to achieve adapter removal, quality control, UMI identification, and generate consensus reads by clustering and error correction using multithreading in high-throughput next-generation sequencing background.RealSeq2also supports methylation data of 5-methylcytosine bisulfite-free sequencing.RealSeq2defined a new tag in SAM for storing methylation information, which is beneficial for co-identifying methylation sites and mutation sites for downstream analysis.RealSeq2includes three submodules: ReadsProfiler, ReadsCleaner, and ReadsRecycler. In addition, the output format file (BAM or SAM) is universal for downstream analyses.RealSeq2is the preferred upstream analysis software for the co-detection of ultra-low frequency mutations and bisulfite-free methylation data. The error profile provides data support for downstream analysis. Additionally, XM tags will become a standard protocol for recording methylation signals.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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