Combining high throughput sequencing with stable isotope probing (HTS-SIP) is a powerful method for mapping in situ metabolic processes to thousands of microbial taxa. However, accurately mapping metabolic processes to taxa is complex and challenging. Multiple HTSSIP data analysis methods have been developed, including high-resolution stable isotope probing (HR-SIP), multi-window high-resolution stable isotope probing (MW-HR-SIP), quantitative stable isotope probing (qSIP), and ΔBD. Currently, there is no publicly available software designed specifically for analyzing HTS-SIP data. To address this shortfall, we have developed the HTSSIP R package, an open-source, cross-platform toolset for conducting HTS-SIP analyses in a straightforward and easily reproducible manner. The HTSSIP package, along with full documentation and examples, is available from CRAN at https://cran.rproject.org/web/packages/HTSSIP/index.html and Github at https://github.com/buckleylab/HTSSIP.
CITATION STYLE
Youngblut, N. D., Barnett, S. E., & Buckley, D. H. (2018). HTSSIP: An r package for analysis of high throughput sequencing data from nucleic acid stable isotope probing (sip) experiments. PLoS ONE, 13(1). https://doi.org/10.1371/journal.pone.0189616
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