Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS

Anne-Katrin Emde, Marcel H. Schulz, David Weese, Ruping Sun, Martin Vingron, Vera M. Kalscheuer, Stefan A. Haas, Knut Reinert. Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. Bioinformatics, 28(5):619-627, 2012. [doi]

@article{EmdeSWSVKHR12,
  title = {Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS},
  author = {Anne-Katrin Emde and Marcel H. Schulz and David Weese and Ruping Sun and Martin Vingron and Vera M. Kalscheuer and Stefan A. Haas and Knut Reinert},
  year = {2012},
  doi = {10.1093/bioinformatics/bts019},
  url = {http://dx.doi.org/10.1093/bioinformatics/bts019},
  researchr = {https://researchr.org/publication/EmdeSWSVKHR12},
  cites = {0},
  citedby = {0},
  journal = {Bioinformatics},
  volume = {28},
  number = {5},
  pages = {619-627},
}