A framework for the detection of de novo mutations in family-based sequencing data

Francioli, Laurent C; Cretu-Stancu, Mircea; Garimella, Kiran V; Fromer, Menachem; Kloosterman, Wigard P; Samocha, Kaitlin E; Neale, Benjamin M; Daly, Mark J; Banks, Eric; DePristo, Mark A; de Bakker, Paul IW; Schönhuth, Alexander

A framework for the detection of de novo mutations in family-based sequencing data

Francioli LC, Cretu-Stancu M, Garimella KV, Fromer M, Kloosterman WP, Samocha KE, Neale BM, Daly MJ, Banks E, DePristo MA, de Bakker PIW, et al. (2016)
European Journal of Human Genetics 25(2): 227-233.

Zeitschriftenaufsatz | Veröffentlicht | Englisch

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DOI

https://doi.org/10.1038/ejhg.2016.147

Autor*in

Francioli, Laurent C; Cretu-Stancu, Mircea; Garimella, Kiran V; Fromer, Menachem; Kloosterman, Wigard P; Samocha, Kaitlin E; Neale, Benjamin M; Daly, Mark J; Banks, Eric; DePristo, Mark A; de Bakker, Paul IW; Schönhuth, Alexander^UniBi

Einrichtung

Technische Fakultät > AG Genome Data Science

Erscheinungsjahr

2016

Zeitschriftentitel

European Journal of Human Genetics

Band

25

Ausgabe

2

Seite(n)

227-233

ISSN

1018-4813

eISSN

1476-5438

Page URI

https://pub.uni-bielefeld.de/record/2941788

Zitieren

Francioli LC, Cretu-Stancu M, Garimella KV, et al. A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics. 2016;25(2):227-233.

Francioli, L. C., Cretu-Stancu, M., Garimella, K. V., Fromer, M., Kloosterman, W. P., Samocha, K. E., Neale, B. M., et al. (2016). A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics, 25(2), 227-233. doi:10.1038/ejhg.2016.147

Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, et al. 2016. “A framework for the detection of de novo mutations in family-based sequencing data”. European Journal of Human Genetics 25 (2): 227-233.

Francioli, L. C., Cretu-Stancu, M., Garimella, K. V., Fromer, M., Kloosterman, W. P., Samocha, K. E., Neale, B. M., Daly, M. J., Banks, E., DePristo, M. A., et al. (2016). A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics 25, 227-233.

Francioli, L.C., et al., 2016. A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics, 25(2), p 227-233.

L.C. Francioli, et al., “A framework for the detection of de novo mutations in family-based sequencing data”, European Journal of Human Genetics, vol. 25, 2016, pp. 227-233.

Francioli, L.C., Cretu-Stancu, M., Garimella, K.V., Fromer, M., Kloosterman, W.P., Samocha, K.E., Neale, B.M., Daly, M.J., Banks, E., DePristo, M.A., de Bakker, P.I.W., Schönhuth, A.: A framework for the detection of de novo mutations in family-based sequencing data. European Journal of Human Genetics. 25, 227-233 (2016).

Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, Daly, Mark J, Banks, Eric, DePristo, Mark A, de Bakker, Paul IW, and Schönhuth, Alexander. “A framework for the detection of de novo mutations in family-based sequencing data”. European Journal of Human Genetics 25.2 (2016): 227-233.

Daten bereitgestellt von European Bioinformatics Institute (EBI)