PANGEA: Pipeline Analysis for Next GEneration Amplicons
High-throughput DNA sequencing can identify organisms and describe population structures in many environmental and clinical samples. Current technologies generate millions of reads in a single run, requiring extensive computational strategies to organize, analyze, and interpret those sequences. A series of bioinformatics tools for high-throughput sequencing analysis, including pre-processing, clustering, database matching, and classification, have been compiled into a pipeline called PANGEA. The PANGEA pipeline was written in Perl and can be run on Mac OSX, Windows or Linux. With PANGEA, sequences obtained directly from the sequencer can be processed quickly to provide the files needed for sequence identification by BLAST and for comparison of microbial communities. Two different sets of bacterial 16S rRNA sequences were used to demonstrate the efficiency of this workflow. The first set of 16S rRNA sequences are derived from various soils from Hawaii Volcanoes National Park. The second set is derived from stools samples collected from diabetes-resistant and diabetes-prone rats. The workflow described here allows the investigator to quickly assess libraries of sequences on personal computers with customized databases. PANGEA is provided for users as individual scripts for each step in the process or as a single script where all processes, except the Chi-square step, are joined into one program called the “backbone”.
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Pangea is hosted on SourceForge.org, https://sourceforge.net/projects/pangea-16s/
Pangea is maintained via Git (A Fast Version Control System) meaning all changes are tracked.