Abstract
AbstractTandem duplication(TD) is a major type ofstructural variation(SV), and plays an important role in novel gene formation and human diseases. However, TDs are often missed or incorrectly classified as insertions by most of modern SV detection methods due to the lacking of specialized operation on TD related mutational signals. Herein, we developed a TD detection module of Pindel referred as Pindel-TD based on a TD specificpattern growthapproach. Pindel-TD detects TDs with a wide size range at single nucleotide resolution. Using simulation and real read data of HG002, we demonstrate that Pindel-TD outperformed other leading methods in terms of precision, recall, F1-score and robustness. Further applying Pindel-TD on data generated from K562 cancer cell line, we identified a TD located at the seventh exon ofSAGE1, explaining its high expression. Pindel-TD is available athttps://github.com/xjtu-omics/pindeland free for non-commercial use.
Publisher
Cold Spring Harbor Laboratory