Identification and prioritization of causal variants of human genetic disorders from exome or whole genome sequencing data

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: OBM Genetics, 2, 2, S.

Event: Veröffentlichung

(where): Augsburg

(who): Universität Augsburg

(when): 2018

Event: Veröffentlichung

(where): Beachwood, OH

(who): LIDSEN Publishing Inc

(when): 2018

Creator: Paramasivam, Nagarajan
Granzow, Martin
Evers, Christina
Hinderhofer, Katrin
Wiemann, Stefan
Bartram, Claus R.
Eils, Roland
Schlesner, Matthias

DOI: 10.21926/obm.genet.1802017

URN: urn:nbn:de:bvb:384-opus4-1034478

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:52 AM CEST

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Associated

Paramasivam, Nagarajan
Granzow, Martin
Evers, Christina
Hinderhofer, Katrin
Wiemann, Stefan
Bartram, Claus R.
Eils, Roland
Schlesner, Matthias
Universität Augsburg
LIDSEN Publishing Inc

Time of origin

2018

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Identification and prioritization of causal variants of human genetic disorders from exome or whole genome sequencing data

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Other Objects (12)

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