E-Health and Bioengineering Conference

Isil Ezgi Eryilmaz; Güney Eskiler, Gamze; Gulsah Cecener; Unal Egeli; Berrin Tunca

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dc.contributor.authors	Eryilmaz, IE; Eskiler, GG; Cecener, G; Egeli, U; Tunca, B;
dc.date.accessioned	2020-02-27T07:21:12Z
dc.date.available	2020-02-27T07:21:12Z
dc.date.issued	2017
dc.identifier.citation	Eryilmaz, IE; Eskiler, GG; Cecener, G; Egeli, U; Tunca, B; (2017). E-Health and Bioengineering Conference. 2017 IEEE INTERNATIONAL CONFERENCE ON E-HEALTH AND BIOENGINEERING CONFERENCE (EHB), , 184-181
dc.identifier.issn	2575-5137
dc.identifier.uri	https://hdl.handle.net/20.500.12619/65545
dc.identifier.uri	https://doi.org/000445457500046
dc.description.abstract	We mentioned the importance of clinical sequence analysis in risk determination, diagnostic and therapeutic process of familial breast cancer and we also summarized next generation sequencing applications in this cancer type. In conclusion, BRCA1/2 genes mutations are associated with an increasing the risk of particularly familial breast cancer. However, sequencing of moderate penetrance genes and/or whole exome could also fill large knowledge gaps in explaining genetic predisposition of breast cancer.
dc.language	English
dc.publisher	IEEE
dc.subject	Medical Informatics
dc.title	E-Health and Bioengineering Conference
dc.type	Proceedings Paper
dc.identifier.startpage	181
dc.identifier.endpage	184
dc.contributor.department	Sakarya Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri Bölümü
dc.contributor.saüauthor	Güney Eskiler, Gamze
dc.relation.journal	2017 IEEE INTERNATIONAL CONFERENCE ON E-HEALTH AND BIOENGINEERING CONFERENCE (EHB)
dc.identifier.wos	WOS:000445457500046
dc.identifier.eissn	2575-5145
dc.contributor.author	Isil Ezgi Eryilmaz
dc.contributor.author	Güney Eskiler, Gamze
dc.contributor.author	Gulsah Cecener
dc.contributor.author	Unal Egeli
dc.contributor.author	Berrin Tunca