Schreiber S - Search Results

1

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software.

Forster M, Forster P, Elsharawy A, Hemmrich G, Kreck B, Wittig M, Thomsen I, Stade B, Barann M, Ellinghaus D, Petersen BS, May S, Melum E, Schilhabel MB, Keller A, Schreiber S, Rosenstiel P, Franke A. Forster M, et al. Among authors: schreiber s. Nucleic Acids Res. 2013 Jan 7;41(1):e16. doi: 10.1093/nar/gks836. Epub 2012 Sep 10. Nucleic Acids Res. 2013. PMID: 22965131 Free PMC article.

2

SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region.

Melum E, May S, Schilhabel MB, Thomsen I, Karlsen TH, Rosenstiel P, Schreiber S, Franke A. Melum E, et al. Among authors: schreiber s. Hum Mutat. 2010 Jul;31(7):875-85. doi: 10.1002/humu.21276. Hum Mutat. 2010. PMID: 20506538

3

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.

Elsharawy A, Forster M, Schracke N, Keller A, Thomsen I, Petersen BS, Stade B, Stähler P, Schreiber S, Rosenstiel P, Franke A. Elsharawy A, et al. Among authors: schreiber s. BMC Genomics. 2012 Aug 22;13:417. doi: 10.1186/1471-2164-13-417. BMC Genomics. 2012. PMID: 22913592 Free PMC article.

4

Accurate variant detection across non-amplified and whole genome amplified DNA using targeted next generation sequencing.

ElSharawy A, Warner J, Olson J, Forster M, Schilhabel MB, Link DR, Rose-John S, Schreiber S, Rosenstiel P, Brayer J, Franke A. ElSharawy A, et al. Among authors: schreiber s. BMC Genomics. 2012 Sep 20;13:500. doi: 10.1186/1471-2164-13-500. BMC Genomics. 2012. PMID: 22994565 Free PMC article.

5

A comprehensive evaluation of SNP genotype imputation.

Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A. Nothnagel M, et al. Among authors: schreiber s. Hum Genet. 2009 Mar;125(2):163-71. doi: 10.1007/s00439-008-0606-5. Epub 2008 Dec 17. Hum Genet. 2009. PMID: 19089453

6

Current software for genotype imputation.

Ellinghaus D, Schreiber S, Franke A, Nothnagel M. Ellinghaus D, et al. Among authors: schreiber s. Hum Genomics. 2009 Jul;3(4):371-80. doi: 10.1186/1479-7364-3-4-371. Hum Genomics. 2009. PMID: 19706367 Free PMC article.

7

CNVineta: a data mining tool for large case-control copy number variation datasets.

Wittig M, Helbig I, Schreiber S, Franke A. Wittig M, et al. Among authors: schreiber s. Bioinformatics. 2010 Sep 1;26(17):2208-9. doi: 10.1093/bioinformatics/btq356. Epub 2010 Jul 6. Bioinformatics. 2010. PMID: 20605930 Free PMC article.

8

Janus--a comprehensive tool investigating the two faces of transcription.

Barann M, Esser D, Klostermeier UC, Lappalainen T, Luzius A, Kuiper JW, Ammerpohl O, Vater I, Siebert R, Amstislavskiy V, Sudbrak R, Lehrach H, Schreiber S, Rosenstiel P. Barann M, et al. Among authors: schreiber s. Bioinformatics. 2013 Jul 1;29(13):1600-6. doi: 10.1093/bioinformatics/btt185. Epub 2013 Apr 24. Bioinformatics. 2013. PMID: 23620359

9

Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.

Petersen BS, Spehlmann ME, Raedler A, Stade B, Thomsen I, Rabionet R, Rosenstiel P, Schreiber S, Franke A. Petersen BS, et al. Among authors: schreiber s. BMC Genomics. 2014 Jul 5;15(1):564. doi: 10.1186/1471-2164-15-564. BMC Genomics. 2014. PMID: 24996980 Free PMC article.

10

GENOMIZER: an integrated analysis system for genome-wide association data.

Franke A, Wollstein A, Teuber M, Wittig M, Lu T, Hoffmann K, Nürnberg P, Krawczak M, Schreiber S, Hampe J. Franke A, et al. Among authors: schreiber s. Hum Mutat. 2006 Jun;27(6):583-8. doi: 10.1002/humu.20306. Hum Mutat. 2006. PMID: 16652332

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