 | 2012 |
|---|
| 8 |       | 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) |
| 7 | | Ruping Sun,
Michael I. Love,
Tomasz Zemojtel,
Anne-Katrin Emde,
Ho-Ryun Chung,
Martin Vingron,
Stefan A. Haas:
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads.
Bioinformatics 28(7): 1024-1025 (2012) |
| 2011 |
|---|
| 6 | | Manuel Holtgrewe,
Anne-Katrin Emde,
David Weese,
Knut Reinert:
A Novel And Well-Defined Benchmarking Method For Second Generation Read Mapping.
BMC Bioinformatics 12: 210 (2011) |
| 2010 |
|---|
| 5 | | Anne-Katrin Emde,
Marcel Grunert,
David Weese,
Knut Reinert,
Silke R. Sperling:
MicroRazerS: rapid alignment of small RNA reads.
Bioinformatics 26(1): 123-124 (2010) |
| 2009 |
|---|
| 4 | | Tobias Rausch,
Sergey Koren,
Gennady Denisov,
David Weese,
Anne-Katrin Emde,
Andreas Döring,
Knut Reinert:
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short reads.
Bioinformatics 25(9): 1118-1124 (2009) |
| 2008 |
|---|
| 3 | | Tobias Rausch,
Anne-Katrin Emde,
David Weese,
Andreas Döring,
Cédric Notredame,
Knut Reinert:
Segment-based multiple sequence alignment.
ECCB 2008: 187-192 |
| 2 | | Tobias Rausch,
Anne-Katrin Emde,
Knut Reinert:
Robust consensus computation.
BMC Bioinformatics 9(S-10): (2008) |
| 2006 |
|---|
| 1 | | Daniel P. Fasulo,
Anne-Katrin Emde,
Lu-Yong Wang,
Karin Noy,
Nathan Edwards:
Alignment of Mass Spectrometry Data by Clique Finding and Optimization.
Systems Biology and Computational Proteomics 2006: 119-129 |
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