Stefan A. Haas

According to our database, Stefan A. Haas authored at least 7 papers between 2002 and 2020.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2020

Ranbow: A fast and accurate method for polyploid haplotype reconstruction.

M-Hossein Moeinzadeh, Jun Yang, Evgeny Muzychenko, Giuseppe Gallone, David Heller, Knut Reinert, Stefan A. Haas, Martin Vingron

PLoS Comput. Biol., 2020

2012

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

Ruping Sun, Michael I. Love, Tomasz Zemojtel, Anne-Katrin Emde, Ho-Ryun Chung, Martin Vingron, Stefan A. Haas

Bioinform., 2012

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

Anne-Katrin Emde, Marcel H. Schulz, David Weese, Ruping Sun, Martin Vingron, Vera M. Kalscheuer, Stefan A. Haas, Knut Reinert

Bioinform., 2012

2009

PASTAA: identifying transcription factors associated with sets of co-regulated genes.

Helge G. Roider, Thomas Manke, Sean O'Keeffe, Martin Vingron, Stefan A. Haas

Bioinform., 2009

2005

T-STAG: resource and web-interface for tissue-specific transcripts and genes.

Shobhit Gupta, Martin Vingron, Stefan A. Haas

Nucleic Acids Res., 2005

2004

Genome wide identification and classification of alternative splicing based on EST data.

Shobhit Gupta, Dorothea Zink, Bernhard Korn, Martin Vingron, Stefan A. Haas

Bioinform., 2004

2002

SYSTERS, GeneNest, SpliceNest: exploring sequence space from genome to protein.

Antje Krause, Stefan A. Haas, Eivind Coward, Martin Vingron

Nucleic Acids Res., 2002