 | 2012 |
|---|
| 6 |       | 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) |
| 5 | | 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) |
| 2009 |
|---|
| 4 | | Helge G. Roider,
Thomas Manke,
Sean O'Keeffe,
Martin Vingron,
Stefan A. Haas:
PASTAA: identifying transcription factors associated with sets of co-regulated genes.
Bioinformatics 25(4): 435-442 (2009) |
| 2005 |
|---|
| 3 | | Shobhit Gupta,
Martin Vingron,
Stefan A. Haas:
T-STAG: resource and web-interface for tissue-specific transcripts and genes.
Nucleic Acids Research 33(Web-Server-Issue): 654-658 (2005) |
| 2004 |
|---|
| 2 | | Shobhit Gupta,
Dorothea Zink,
Bernhard Korn,
Martin Vingron,
Stefan A. Haas:
Genome wide identification and classification of alternative splicing based on EST data.
Bioinformatics 20(16): 2579-2585 (2004) |
| 2002 |
|---|
| 1 | | Antje Krause,
Stefan A. Haas,
Eivind Coward,
Martin Vingron:
SYSTERS, GeneNest, SpliceNest: exploring sequence space from genome to protein.
Nucleic Acids Research 30(1): 299-300 (2002) |
Data released under the ODC-BY 1.0 license — See also our legal information page