The matter of clinical sequencing for familial breast cancer: The route from Sanger to next generation

Simple item page
dc.contributor.authorEskiler, Gamze Güney
dc.contributor.buuauthorEryılmaz, Işıl Ezgi
dc.contributor.buuauthorÇeçener, Gülşah
dc.contributor.buuauthorEgeli, Ünal
dc.contributor.buuauthorTunca, Berrin
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-3316-316Xtr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.contributor.orcid0000-0002-3820-424Xtr_TR
dc.contributor.orcid0000-0002-3316-316Xtr_TR
dc.contributor.orcid0000-0001-7904-883Xtr_TR
dc.contributor.researcheridGWV-3548-2022tr_TR
dc.contributor.researcheridABI-6078-2020tr_TR
dc.contributor.researcheridAAP-9988-2020tr_TR
dc.contributor.researcheridAAH-1656-2021tr_TR
dc.contributor.researcheridAAH-1420-2021tr_TR
dc.contributor.scopusid57189380840tr_TR
dc.contributor.scopusid6508156530tr_TR
dc.contributor.scopusid55665145000tr_TR
dc.contributor.scopusid6602965754tr_TR
dc.date.accessioned2023-08-11T07:12:51Z
dc.date.available2023-08-11T07:12:51Z
dc.date.issued2017
dc.descriptionBu çalışma, 22-24 Haziran 2017 tarihlerinde Sinaia[Romanya]’da düzenlenen 6. IEEE International Conference on E-Health and Bioengineering (EHB) Kongresi‘nde bildiri olarak sunulmuştur.tr_TR
dc.description.abstractWe 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.en_US
dc.description.sponsorshipIEEEen_US
dc.description.sponsorshipIEEE EMB Romania Chapteren_US
dc.description.sponsorshipRomanian Acad, Iasi Branch, Inst Comp Scien_US
dc.description.sponsorshipGrigore T Popa Univ Med & Pharmacyen_US
dc.description.sponsorshipIEEE Romania Secten_US
dc.description.sponsorshipInst Informatica Teoreticaen_US
dc.description.sponsorshipESC Working Grp e Cardiolen_US
dc.description.sponsorshipRomanian Soc Med Bioengineeringen_US
dc.description.sponsorshipGrigore T Popa Univ Med & Pharmacy, Fac Med Bioengineeringen_US
dc.description.sponsorshipIEEE EMC Romania Chapteren_US
dc.identifier.citationEryılmaz, I. E. vd. (2017). ''The matter of clinical sequencing for familial breast cancer: The route from Sanger to next generation''. E-Health and Bioengineering Conference, 2017 IEEE Internatıonal conference on E-health and bioengineerıng conference (EHB), 181-184.en_US
dc.identifier.endpage184tr_TR
dc.identifier.isbn978-1-5386-0358-1
dc.identifier.issn2575-5137
dc.identifier.issn2575-5145
dc.identifier.scopus2-s2.0-85028568022tr_TR
dc.identifier.startpage181tr_TR
dc.identifier.urihttp://hdl.handle.net/11452/33469
dc.identifier.wos000445457500046
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherIEEEen_US
dc.relation.collaborationYurt içitr_TR
dc.relation.journal2017 Ieee Internatıonal Conference on E-Health And Bıoengıneerıng Conference (EHB)en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararasıtr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectComputer scienceen_US
dc.subjectEngineeringen_US
dc.subjectMedical informaticsen_US
dc.subjectGenesen_US
dc.subjectRisk analysisen_US
dc.subjectRisk assessmenten_US
dc.subjectFamilial breast canceren_US
dc.subjectNext generation sequencingen_US
dc.subjectEarly-onseten_US
dc.subjectInherited mutationsen_US
dc.subjectDna-repairen_US
dc.subjectRisken_US
dc.subjectBrca1en_US
dc.subjectAssociationen_US
dc.subjectVariantsen_US
dc.subjectPalb2en_US
dc.subjectBreast canceren_US
dc.subjectGenes mutationen_US
dc.subjectGenetic predispositionen_US
dc.subjectKnowledge gapsen_US
dc.subjectNext-generation sequencingen_US
dc.subjectRisk determinationen_US
dc.subjectSanger sequencingen_US
dc.subjectSequence analysisen_US
dc.subjectDiseasesen_US
dc.subject.scopusFamilial Breast Cancer; Partner and Localizer of BRCA2; Breast Neoplasmsen_US
dc.subject.wosComputer science, interdisciplinary applicationsen_US
dc.subject.wosEngineering, biomedicalen_US
dc.subject.wosMedical informaticsen_US
dc.titleThe matter of clinical sequencing for familial breast cancer: The route from Sanger to next generationen_US
dc.typeProceedings Paper

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description:
Download

Collections

Web of Science
Scopus