Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hannane Mohammadi"'
Publikováno v:
Journal of Medical Signals and Sensors, Vol 11, Iss 1, Pp 37-44 (2021)
Background: Careful design in the primary steps of a next-generation sequencing study is critical for obtaining successful results in downstream analysis. Methods: In this study, a framework is proposed to evaluate and improve the sequence mapping in
Externí odkaz:
https://doaj.org/article/2baf8952ea0f49b09ad63a3245b6d207
Autor:
Mohammad Reza Pourreza, Hannane Mohammadi, Ladan Sadeghian, Samira Asgharzadeh, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar
Publikováno v:
Advanced Biomedical Research, Vol 7, Iss 1, Pp 141-141 (2018)
Background: Hearing loss (HL) is a highly prevalent heterogeneous deficiency of sensory-neural system with involvement of several dozen genes. Whole-exome sequencing (WES) is capable of discovering known and novel genes involved with HL. Materials an
Externí odkaz:
https://doaj.org/article/2d315402b9714eda880e30184f734faa
Autor:
Nodehi, Hannane Mohammadi1 hannane.mohammadi@gmail.com, Tabatabaiefar, Mohammad Amin2,3 tabatabaiefar@med.mui.ac.ir, Sehhati, Mohammadreza1 mr.sehhati@gmail.com
Publikováno v:
Journal of Medical Signals & Sensors. Jan-Mar2021, Vol. 11 Issue 1, p37-44. 8p.
Publikováno v:
Journal of Medical Signals and Sensors
Journal of Medical Signals and Sensors, Vol 11, Iss 1, Pp 37-44 (2021)
Journal of Medical Signals and Sensors, Vol 11, Iss 1, Pp 37-44 (2021)
Background: Careful design in the primary steps of a next-generation sequencing study is critical for obtaining successful results in downstream analysis. Subjects and Methods: In this study, a framework is proposed to evaluate and improve the sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b0b73e5563622be3fa10ad1c0cc5f4e
http://europepmc.org/articles/PMC8043119
http://europepmc.org/articles/PMC8043119
Autor:
Mohammadreza Sehhati, Hannane Mohammadi, Ladan Sadeghian, Mohammad Amin Tabatabaiefar, Samira Asgharzadeh, Mohammad Reza Pourreza
Publikováno v:
Advanced Biomedical Research, Vol 7, Iss 1, Pp 141-141 (2018)
Advanced Biomedical Research
Advanced Biomedical Research
Background: Hearing loss (HL) is a highly prevalent heterogeneous deficiency of sensory-neural system with involvement of several dozen genes. Whole-exome sequencing (WES) is capable of discovering known and novel genes involved with HL. Materials an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87207cc2d94524086d3b5422b937bb4
http://www.advbiores.net/article.asp?issn=2277-9175
http://www.advbiores.net/article.asp?issn=2277-9175