Analytical Genomics / Biology of Genomes / Publications

Ulysses: accurate detection of low-frequency structural variations in large insert-size sequencing libraries.

Gillet-Markowska A., Richard H., Fischer G., Lafontaine I. Bioinformatics (2015)

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15 March 2015

Analytical Genomics / Publications

The diversity of small non-coding RNAs in the diatom Phaeodactylum tricornutum.

Rogato A., Richard H., Sarazin A., Voss B., Cheminant Navarro S., Champeimont R., Navarro L., Carbone A., Hess W., Falciatore A. BMC Genomics (2014)

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1 December 2014

Analytical Genomics / Publications

Fiona: a parallel and automatic strategy for read error correction

Schulz M., Weese D., Holtgrewe M., Dimitrova V., Niu S., Reinert K., Richard H. Bioinformatics (2014)

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1 September 2014

Analytical Genomics / Publications

Parseq: reconstruction of microbial transcription landscape from RNA-Seq read counts using state-space models.

Mirauta B., Nicolas P., Richard H. Bioinformatics (2014)

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1 January 2014

Analytical Genomics / Publications

Pardiff: Inference of Differential Expression at Base-Pair Level from RNA-Seq Experiments

Mirauta B., Nicolas P., Richard H. Lecture Notes in Computer Science (2013)

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1 January 2013

Analytical Genomics / Publications

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.

Hu H., Wrogemann K., Kalscheuer V., Tzschach A., Richard H., Haas S., Menzel C., Bienek M., Froyen G., Raynaud M., Van Bokhoven H., Chelly J., Ropers H., Chen W. The HUGO Journal (2009)

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1 December 2009

Analytical Genomics / Publications

A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome.

Sultan M., Schulz M., Richard H., Magen A., Klingenhoff A., Scherf M., Seifert M., Borodina T., Soldatov A., Parkhomchuk D., Schmidt D., O'Keeffe S., Haas S., Vingron M., Lehrach H., Yaspo M. Science (2008)

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15 August 2008