PHFinder: assisted detection of point heteroplasmy in Sanger sequencing chromatograms

• Published in: PeerJ
• Main Authors: Suárez Menéndez, Marcos, Rivera-León, Vania E., Robbins, Jooke, Berube, Martine, Palsbøll, Per J.
• Other Authors: The University of Groningen
• Format: Article in Journal/Newspaper
• Language: English
• Published: PeerJ 2023
• Subjects: Megaptera novaeangliae
• Online Access: http://dx.doi.org/10.7717/peerj.16028; https://peerj.com/articles/16028.pdf; https://peerj.com/articles/16028.xml; https://peerj.com/articles/16028.html

Heteroplasmy is the presence of two or more organellar genomes (mitochondrial or plastid DNA) in an organism, tissue, cell or organelle. Heteroplasmy can be detected by visual inspection of Sanger sequencing chromatograms, where it appears as multiple peaks of fluorescence at a single nucleotide position. Visual inspection of chromatograms is both consuming and highly subjective, as heteroplasmy is difficult to differentiate from background noise. Few software solutions are available to automate the detection of point heteroplasmies, and those that are available are typically proprietary, lack customization or are unsuitable for automated heteroplasmy assessment in large datasets. Here, we present PHFinder, a Python-based, open-source tool to assist in the detection of point heteroplasmies in large numbers of Sanger chromatograms. PHFinder automatically identifies point heteroplasmies directly from the chromatogram trace data. The program was tested with Sanger sequencing data from 100 humpback whales ( Megaptera novaeangliae ) tissue samples with known heteroplasmies. PHFinder detected most (90%) of the known heteroplasmies thereby greatly reducing the amount of visual inspection required. PHFinder is flexible and enables explicit specification of key parameters to infer double peaks ( i.e. , heteroplasmies).