Science AdvancesBioinformaticsPeer-reviewed journal article
A universal sequencing read interpreter
Yusuke KijimaiD, Daniel Evans-YamamotoiD, Hiromi ToyoshimaiD, Nozomu YachieiD
Abstract
Massively parallel DNA sequencing has led to the rapid growth of highly multiplexed experiments in biology. Such experiments produce unique sequencing results that require specific analysis pipelines to decode highly structured reads. However, no versatile framework that interprets sequencing reads for downstream biological analysis has been developed. Here we report INTERSTELLAR (interpretation, scalable transformation, and emulation of large-scale sequencing reads) that extracts data values encoded in theoretically any type of sequencing read and translates them into sequencing reads of any structure of choice. INTERSTELLAR first identifies sequence segments encoded in reads according to the users definition. Followed by error correction, values are extracted and compressed into an optimal space, which can be efficiently translated into sequencing reads of another structure. We demonstrated that INTERSTELLAR successfully extracted information from a range of sequencing reads and translated those of single-cell (sc)RNA-seq, scATAC-seq, and spatial transcriptomics to be analyzed by different software tools that have been developed for conceptually the same types of experiments. INTERSTELLAR will greatly facilitate the development of new sequencing-based experiments and sharing of data analysis pipelines.
- assay: DNA methylation
- assay: whole-genome sequencing
- assay: whole-exome sequencing
- assay: long-read sequencing
- research focus: benchmarking
- research focus: software / tool
- research focus: dimensionality reduction
- approach: experimental assay
- Citations
- 7
- FWCI
- 0.62
- Field percentile
- top 42%
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