Emde, Anne-Katrin <br/><br/>
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.  [electronic resource] 

 -  Bioinformatics (Oxford, England)  Mar 2012 
 - 619-27 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1367-4811 
<br/><br/><label>Standard No.: </label>10.1093/bioinformatics/bts019  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Algorithms<br/>Genomics--methods<br/>Humans<br/>INDEL Mutation<br/>Sequence Analysis, DNA