Anne-Katrin Emde

According to our database1, Anne-Katrin Emde authored at least 10 papers between 2006 and 2014.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

On csauthors.net:

Bibliography

2014
Gustaf: Detecting and correctly classifying SVs in the NGS twilight zone.
Bioinform., 2014

2013
Next-generation sequencing algorithms: from read mapping to variant detection.
PhD thesis, 2013

2012
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads.
Bioinform., 2012

Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.
Bioinform., 2012

2011
A Novel And Well-Defined Benchmarking Method For Second Generation Read Mapping.
BMC Bioinform., 2011

2010
MicroRazerS: rapid alignment of small RNA reads.
Bioinform., 2010

2009
A consistency-based consensus algorithm for <i>de novo</i> and reference-guided sequence assembly of short reads.
Bioinform., 2009

2008
Robust consensus computation.
BMC Bioinform., 2008

Segment-based multiple sequence alignment.
Proceedings of the ECCB'08 Proceedings, 2008

2006
Alignment of Mass Spectrometry Data by Clique Finding and Optimization.
Proceedings of the Systems Biology and Computational Proteomics, 2006


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