Abstract
Background: While active LINE-1 (L1) elements possess the ability to mobilize flanking sequences to different genomic loci through a process termed transduction influencing genomic content and structure, an approach for detecting polymorphic germline non-reference transductions in massively-parallel sequencing data has been lacking. Results: Here we present the computational approach TIGER (Transduction Inference in GERmline genomes), enabling the discovery of non-reference L1-mediated transductions by combining L1 discovery with detection of unique insertion sequences and detailed characterization of insertion sites. We employed TIGER to characterize polymorphic transductions in fifteen genomes from non-human primate species (chimpanzee, orangutan and rhesus macaque), as well as in a human genome. We achieved high accuracy as confirmed by PCR and two single molecule DNA sequencing techniques, and uncovered differences in relative rates of transduction between primate species. Conclusions: By enabling detection of polymorphic transductions, TIGER makes this form of relevant structural variation amenable for population and personal genome analysis.
| Original language | English |
|---|---|
| Article number | 342 |
| Journal | BMC Genomics |
| Volume | 17 |
| Issue number | 1 |
| DOIs | |
| State | Published - May 10 2016 |
Keywords
- Bioinformatics
- Genetics
- Genome
- L1
- NGS
- Primates
- Retrotransposon
- Single-molecule sequencing
- Transductions
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