Publication:
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.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Biyoloji Ana Bilim Dalı
dc.contributor.orcid0000-0002-3316-316X
dc.contributor.orcid0000-0002-1619-6680
dc.contributor.orcid0000-0002-3820-424X
dc.contributor.orcid0000-0002-3316-316X
dc.contributor.orcid0000-0001-7904-883X
dc.contributor.researcheridGWV-3548-2022
dc.contributor.researcheridABI-6078-2020
dc.contributor.researcheridAAP-9988-2020
dc.contributor.researcheridAAH-1656-2021
dc.contributor.researcheridAAH-1420-2021
dc.contributor.scopusid57189380840
dc.contributor.scopusid6508156530
dc.contributor.scopusid55665145000
dc.contributor.scopusid6602965754
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.
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.
dc.description.sponsorshipIEEE
dc.description.sponsorshipIEEE EMB Romania Chapter
dc.description.sponsorshipRomanian Acad, Iasi Branch, Inst Comp Sci
dc.description.sponsorshipGrigore T Popa Univ Med & Pharmacy
dc.description.sponsorshipIEEE Romania Sect
dc.description.sponsorshipInst Informatica Teoretica
dc.description.sponsorshipESC Working Grp e Cardiol
dc.description.sponsorshipRomanian Soc Med Bioengineering
dc.description.sponsorshipGrigore T Popa Univ Med & Pharmacy, Fac Med Bioengineering
dc.description.sponsorshipIEEE EMC Romania Chapter
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.
dc.identifier.endpage184
dc.identifier.isbn978-1-5386-0358-1
dc.identifier.issn2575-5137
dc.identifier.issn2575-5145
dc.identifier.scopus2-s2.0-85028568022
dc.identifier.startpage181
dc.identifier.urihttp://hdl.handle.net/11452/33469
dc.identifier.wos000445457500046
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherIEEE
dc.relation.collaborationYurt içi
dc.relation.journal2017 Ieee Internatıonal Conference on E-Health And Bıoengıneerıng Conference (EHB)
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectComputer science
dc.subjectEngineering
dc.subjectMedical informatics
dc.subjectGenes
dc.subjectRisk analysis
dc.subjectRisk assessment
dc.subjectFamilial breast cancer
dc.subjectNext generation sequencing
dc.subjectEarly-onset
dc.subjectInherited mutations
dc.subjectDna-repair
dc.subjectRisk
dc.subjectBrca1
dc.subjectAssociation
dc.subjectVariants
dc.subjectPalb2
dc.subjectBreast cancer
dc.subjectGenes mutation
dc.subjectGenetic predisposition
dc.subjectKnowledge gaps
dc.subjectNext-generation sequencing
dc.subjectRisk determination
dc.subjectSanger sequencing
dc.subjectSequence analysis
dc.subjectDiseases
dc.subject.scopusFamilial Breast Cancer; Partner and Localizer of BRCA2; Breast Neoplasms
dc.subject.wosComputer science, interdisciplinary applications
dc.subject.wosEngineering, biomedical
dc.subject.wosMedical informatics
dc.titleThe matter of clinical sequencing for familial breast cancer: The route from Sanger to next generation
dc.typeProceedings Paper
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Biyoloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

Files

License bundle

Now showing 1 - 1 of 1
Placeholder
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description:
Download

Collections

İndeksli Yayınlar / Indexed Publications