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• W2938989721 abstract "Transposable elements make up a significant portion of the human genome. Accurately locating these mobile DNAs is vital to understand their role as a source of structural variation and somatic mutation. To this end, laboratories have developed strategies to selectively amplify or otherwise enrich transposable element insertion sites in genomic DNA. Here we describe a technique, Transposon Insertion Profiling by sequencing (TIPseq), to map Long INterspersed Element 1 (LINE-1, L1) retrotransposon insertions in the human genome. This method uses vectorette PCR to amplify species-specific L1 (L1PA1) insertion sites followed by paired-end Illumina sequencing. In addition to providing a step-by-step molecular biology protocol, we offer users a guide to our pipeline for data analysis, TIPseqHunter. Our recent studies in pancreatic and ovarian cancer demonstrate the ability of TIPseq to identify invariant (fixed), polymorphic (inherited variants), as well as somatically-acquired L1 insertions that distinguish cancer genomes from a patient’s constitutional make-up. TIPseq provides an approach for amplifying evolutionarily young, active transposable element insertion sites from genomic DNA. Our rationale and variations on this protocol may be useful to those mapping L1 and other mobile elements in complex genomes." @default.
• W2938989721 created "2019-04-25" @default.
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• W2938989721 date "2019-03-08" @default.
• W2938989721 modified "2023-10-15" @default.
• W2938989721 title "Transposon insertion profiling by sequencing (TIPseq) for mapping LINE-1 insertions in the human genome" @default.
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• W2938989721 doi "https://doi.org/10.1186/s13100-019-0148-5" @default.
• W2938989721 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6407172" @default.
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