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Fluidigm2PURC: Automated processing and haplotype inference for double-barcoded PCR amplicons
Paul D Blischak1, Maribeth Latvis2, Diego F Morales-Briones3
1Department of Evolution, Ecology, and Organismal Biology The Ohio State University 318 W. 12th Avenue Columbus Ohio 43210-1242 USA.
This study introduces Fluidigm2PURC, a Python tool that automates DNA data processing for phylogenomic studies. It works with paired-end Illumina data to infer haplotypes for various ploidy levels, enhancing phylogenetic research efficiency.
Area of Science:
- Genomics
- Bioinformatics
- Evolutionary Biology
Background:
- Targeted enrichment strategies efficiently collect DNA sequence data for phylogenomic inference.
- Automated and reproducible data processing is essential for phylogenetic studies.
Purpose of the Study:
- To present Fluidigm2PURC, an open-source Python utility for processing paired-end Illumina data.
- To enable automated and reproducible analysis of phylogenomic data.
Main Methods:
- Developed Fluidigm2PURC, a Python utility for processing double-barcoded PCR amplicon data.
- Integrated Fluidigm2PURC with the PURC (Pipeline for Untangling Reticulate Complexes) program.
- Processed raw FASTQ files for PURC analysis and inferred haplotypes for various ploidy levels.
Main Results:
- Fluidigm2PURC successfully processes paired-end Illumina data.
- The pipeline infers haplotypes for diploids, polyploids, and samples with unknown ploidy.
- Demonstrated utility with a dataset from the genus Thalictrum (Ranunculaceae).
Conclusions:
- Fluidigm2PURC is freely available on GitHub for Unix-like systems.
- The utility is also accessible via Docker for all operating systems.
- Fluidigm2PURC facilitates efficient and reproducible phylogenomic data analysis.
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