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Items: 6

1.

Next-generation diagnostics and disease-gene discovery with the Exomiser.

Smedley D, Jacobsen JO, Jäger M, Köhler S, Holtgrewe M, Schubach M, Siragusa E, Zemojtel T, Buske OJ, Washington NL, Bone WP, Haendel MA, Robinson PN.

Nat Protoc. 2015 Dec;10(12):2004-15. doi: 10.1038/nprot.2015.124. Epub 2015 Nov 12.

PMID:
26562621
2.

Methods for the detection and assembly of novel sequence in high-throughput sequencing data.

Holtgrewe M, Kuchenbecker L, Reinert K.

Bioinformatics. 2015 Jun 15;31(12):1904-12. doi: 10.1093/bioinformatics/btv051. Epub 2015 Feb 2.

PMID:
25649620
3.

Fiona: a parallel and automatic strategy for read error correction.

Schulz MH, Weese D, Holtgrewe M, Dimitrova V, Niu S, Reinert K, Richard H.

Bioinformatics. 2014 Sep 1;30(17):i356-63. doi: 10.1093/bioinformatics/btu440.

4.

Genome alignment with graph data structures: a comparison.

Kehr B, Trappe K, Holtgrewe M, Reinert K.

BMC Bioinformatics. 2014 Apr 9;15:99. doi: 10.1186/1471-2105-15-99.

5.

RazerS 3: faster, fully sensitive read mapping.

Weese D, Holtgrewe M, Reinert K.

Bioinformatics. 2012 Oct 15;28(20):2592-9. doi: 10.1093/bioinformatics/bts505. Epub 2012 Aug 24.

6.

A novel and well-defined benchmarking method for second generation read mapping.

Holtgrewe M, Emde AK, Weese D, Reinert K.

BMC Bioinformatics. 2011 May 26;12:210. doi: 10.1186/1471-2105-12-210.

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