A machine-readable specification for genomics assays
- PMID: 38579259
- PMCID: PMC11009023
- DOI: 10.1093/bioinformatics/btae168
A machine-readable specification for genomics assays
Abstract
Motivation: Understanding the structure of sequenced fragments from genomics libraries is essential for accurate read preprocessing. Currently, different assays and sequencing technologies require custom scripts and programs that do not leverage the common structure of sequence elements present in genomics libraries.
Results: We present seqspec, a machine-readable specification for libraries produced by genomics assays that facilitates standardization of preprocessing and enables tracking and comparison of genomics assays.
Availability and implementation: The specification and associated seqspec command line tool is available at https://www.doi.org/10.5281/zenodo.10213865.
© The Author(s) 2024. Published by Oxford University Press.
Conflict of interest statement
None declared.
Figures
Update of
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A machine-readable specification for genomics assays.bioRxiv [Preprint]. 2023 Jul 18:2023.03.17.533215. doi: 10.1101/2023.03.17.533215. bioRxiv. 2023. Update in: Bioinformatics. 2024 Mar 29;40(4):btae168. doi: 10.1093/bioinformatics/btae168. PMID: 36993635 Free PMC article. Updated. Preprint.
References
-
- Chen X. Collections of library structure and sequence of popular single cell genomic methods. GitHub. 2020. https://github.com/Teichlab/scg_lib_structs.
-
- Cheow LF, Courtois ET, Tan Y. et al. Single-cell multimodal profiling reveals cellular epigenetic heterogeneity. Nat Methods 2016;13:833–6. - PubMed
-
- Healey HM, Bassham S, Cresko WA.. Single-cell iso-sequencing enables rapid genome annotation for scRNAseq analysis. Genetics 2022;220. https://academic.oup.com/genetics/article/220/3/iyac017/6526397. - PMC - PubMed
