APA

Emde A., Schulz M. H., Weese D., Sun R., Vingron M., Kalscheuer V. M., Haas S. A. & Reinert K. (20120810). Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. : Bioinformatics (Oxford, England).

Chicago

Emde Anne-Katrin, Schulz Marcel H, Weese David, Sun Ruping, Vingron Martin, Kalscheuer Vera M, Haas Stefan A and Reinert Knut. 20120810. Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. : Bioinformatics (Oxford, England).

Harvard

Emde A., Schulz M. H., Weese D., Sun R., Vingron M., Kalscheuer V. M., Haas S. A. and Reinert K. (20120810). Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. : Bioinformatics (Oxford, England).

MLA

Emde Anne-Katrin, Schulz Marcel H, Weese David, Sun Ruping, Vingron Martin, Kalscheuer Vera M, Haas Stefan A and Reinert Knut. Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. : Bioinformatics (Oxford, England). 20120810.