Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ahmet Rasit Ozturk"'
Publikováno v:
BMC Genomics, Vol 21, Iss 1, Pp 1-16 (2020)
Abstract Background The emergence of high throughput technologies that produce vast amounts of genomic data, such as next-generation sequencing (NGS) is transforming biological research. The dramatic increase in the volume of data, the variety and co
Externí odkaz:
https://doaj.org/article/a37c29437e014b29967d833c720d2829
Autor:
Krishna S Ghanta, Zexiang Chen, Aamir Mir, Gregoriy A Dokshin, Pranathi M Krishnamurthy, Yeonsoo Yoon, Judith Gallant, Ping Xu, Xiao-Ou Zhang, Ahmet Rasit Ozturk, Masahiro Shin, Feston Idrizi, Pengpeng Liu, Hassan Gneid, Alireza Edraki, Nathan D Lawson, Jaime A Rivera-Pérez, Erik J Sontheimer, Jonathan K Watts, Craig C Mello
Publikováno v:
eLife, Vol 10 (2021)
Nuclease-directed genome editing is a powerful tool for investigating physiology and has great promise as a therapeutic approach to correct mutations that cause disease. In its most precise form, genome editing can use cellular homology-directed repa
Externí odkaz:
https://doaj.org/article/a4d2a8d974e94e189ee441394236bb61
Autor:
Ahmet Rasit Ozturk, Tolga Can
Publikováno v:
BMC Bioinformatics, Vol 18, Iss 1, Pp 1-9 (2017)
Abstract Background Targeted Next Generation Sequencing (NGS) assays are cost-efficient and reliable alternatives to Sanger sequencing. For sequencing of very large set of genes, the target enrichment approach is suitable. However, for smaller genomi
Externí odkaz:
https://doaj.org/article/169c4f0696014e87b54079de63fd6cfb
Autor:
Betül Bozkurt, Isik G. Yulug, Gülüşan Ergül, Bala Gur-Dedeoglu, Ozlen Konu, Serkan Kir, Ahmet Rasit Ozturk
Publikováno v:
BMC Genomics
BMC Cancer, Vol 8, Iss 1, p 396 (2008)
BMC Cancer
BMC Cancer, Vol 8, Iss 1, p 396 (2008)
BMC Cancer
BackgroundAccuracy in the diagnosis of breast cancer and classification of cancer subtypes has improved over the years with the development of well-established immunohistopathological criteria. More recently, diagnostic gene-sets at the mRNA expressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467a1319300844e8da19f852aecfd6b9
https://aperta.ulakbim.gov.tr/record/41529
https://aperta.ulakbim.gov.tr/record/41529
Autor:
Fatih Bayrakli, Bulent Guclu, Ünal Özüm, Burak Kazanci, Ahmet Rasit Ozturk, Cengiz Yakicier, Hamit Zafer Kars, Mahmut Şamil Sağıroğlu, Şirin Yüksel, Hatice Balaban, Ugur Kartal, Bekir Ergüner
Publikováno v:
BMC Genetics
WOS: 000325205700001
PubMed ID: 24073994
Background: Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes. Affected individuals who are the children of a c
PubMed ID: 24073994
Background: Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes. Affected individuals who are the children of a c