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Short description:
Please summarise the application in a few sentences. Avoid links here. Identifies paired-end reads which overlap in the middle, converting them to single long reads
Software version:
Biological application domain(s) (Phylogenetics, Genomics, ...):
Principal bioinformatics method(s) (Assembly, Mapping, ...):
Sequence assembly, Read pre-processing
Technology (Sanger, Illumina, 454, SOLiD, Ion Torrent, ...):
Interface (Command line, Web UI, Desktop GUI, SOAP WS, HTTP WS, API, QL):
Resource type (Command-line tool, Web application, Desktop application, Script, Suite, Workbench, Database portal, Workflow, Plug-in, Library, Web API, Web service, SPARQL endpoint):
== Description == <!-- Describe the application in the space below --> This application combines overlapping forward and reverse reads into one long read. It takes about 2 minutes to combine 1 million 2x100 bp reads on a dual core Xeon and up. A problem might arise with perfectly repeated regions in the overlap, as this can get collapsed. <!-- -->
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