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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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, AlexanderUniBi 
Alle
Alle
Einrichtung
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.
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