Data Analysis for DNA Stable Isotope Probing Experiments Using Multiple Window High-Resolution SIP

Author(s):  
Samuel E. Barnett ◽  
Nicholas D. Youngblut ◽  
Daniel H. Buckley
2010 ◽  
Vol 16 (S2) ◽  
pp. 426-427
Author(s):  
X Mayali ◽  
PK Weber ◽  
EL Brodie ◽  
S Mabery ◽  
PD Hoeprich ◽  
...  

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.


2017 ◽  
Vol 9 (15) ◽  
pp. 2275-2283 ◽  
Author(s):  
X. Wei ◽  
P. K. Lorkiewicz ◽  
B. Shi ◽  
J. K. Salabei ◽  
B. G. Hill ◽  
...  

Developed a suite of data analysis algorithms for automatic analysis of SIAM data acquired on a high resolution mass spectrometer.


2017 ◽  
Author(s):  
Nicholas D. Youngblut ◽  
Samuel E. Barnett ◽  
Daniel H. Buckley

AbstractCombining 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 HTS-SIP 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 (q-SIP), and ΔBD. Currently, the computational tools to perform these analyses are either not publicly available or lack documentation, testing, and developer support. To address this shortfall, we have developed the HTSSIP R package, a 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.r-project.org/web/packages/HTSSIP/index.html and Github at https://github.com/nick-youngblut/HTSSIP.


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