Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads
Year: 2012
Type: article
Abstract: SUMMARY: We developed Breakpointer, a fast algorithm to locate breakpoints of structural variants (SVs) from single-end reads produced by next-generation sequencing. By taking advantage of local non-uniform read distribution and misalignments created by SVs, Breakpointer scans the alignment of single-end reads to identify regions containing potential breakpoints. The detection of such breakpoints can indicate insertions longer than the read length and SVs located in repetitve regions which might be missd by other methods. Thus, Breakpointer complements existing methods to locate SVs from single-end reads. AVAILABILITY: https://github.com/ruping/Breakpointer CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary material is available at Bioinformatics online.
Source: Bioinformatics
Institution: Max Planck Institute for Molecular Genetics
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
Funder: Max-Planck-Gesellschaft
OpenAlex ID: W2159603617
