I was one of two presenters (along only with Damon Little of the New York Botanical Garden) to a subset of the Plant Working Group invited to the Edinburgh Conference """"""""Selecting Barcode Loci for Plants"""""""" specifically to analyze standardized data, to select a plant barcode. The other conference participants sequenced seven candidate barcode loci across a broad range of land plants. Damon and I analyzed the resulting data, so the conference participants could select loci to constitute a plant barcode. The Edinburgh Conference selected rbcL and matK as the two plant barcode loci.
Suwannasai, Nuttika; Martin, Maria P; Phosri, Cherdchai et al. (2013) Fungi in Thailand: a case study of the efficacy of an ITS barcode for automatically identifying species within the Annulohypoxylon and Hypoxylon genera. PLoS One 8:e54529 |
Pawlowski, Jan; Audic, Stephane; Adl, Sina et al. (2012) CBOL protist working group: barcoding eukaryotic richness beyond the animal, plant, and fungal kingdoms. PLoS Biol 10:e1001419 |
Schoch, Conrad L; Seifert, Keith A; Huhndorf, Sabine et al. (2012) Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi. Proc Natl Acad Sci U S A 109:6241-6 |
Spouge, John L; Mariño-Ramírez, Leonardo (2012) The practical evaluation of DNA barcode efficacy. Methods Mol Biol 858:365-77 |
CBOL Plant Working Group (2009) A DNA barcode for land plants. Proc Natl Acad Sci U S A 106:12794-7 |