Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ofer Zelig"'
Autor:
Shalini Aggarwal, Chana Rosenblum, Marshall Gould, Shahar Ziman, Ruth Barshir, Ofer Zelig, Yaron Guan-Golan, Tsippi Iny-Stein, Marilyn Safran, Shmuel Pietrokovski, Doron Lancet
Publikováno v:
Biomedicines, Vol 12, Iss 6, p 1305 (2024)
The GeneCaRNA human gene database is a member of the GeneCards Suite. It presents ~280,000 human non-coding RNA genes, identified algorithmically from ~690,000 RNAcentral transcripts. This expands by ~tenfold the ncRNA gene count relative to other so
Externí odkaz:
https://doaj.org/article/8167371f30ce4c568404f20a426f5206
Autor:
Dvir Dahary, Yaron Golan, Yaron Mazor, Ofer Zelig, Ruth Barshir, Michal Twik, Tsippi Iny Stein, Guy Rosner, Revital Kariv, Fei Chen, Qiang Zhang, Yiping Shen, Marilyn Safran, Doron Lancet, Simon Fishilevich
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-17 (2019)
Abstract Background The clinical genetics revolution ushers in great opportunities, accompanied by significant challenges. The fundamental mission in clinical genetics is to analyze genomes, and to identify the most relevant genetic variations underl
Externí odkaz:
https://doaj.org/article/4b87794257854274bfbe57b3b3799db9
Autor:
Doron Lancet, Dvir Dahary, Tsippi Iny Stein, Ofer Zelig, Ruth Barshir, Marilyn Safran, Yaron Mazor, Fei Chen, Guy Rosner, Yiping Shen, Michal Twik, Yaron Golan, Revital Kariv, Simon Fishilevich, Qiang Zhang
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-17 (2019)
BMC Medical Genomics
BMC Medical Genomics
BackgroundThe clinical genetics revolution ushers in great opportunities, accompanied by significant challenges. The fundamental mission in clinical genetics is to analyze genomes, and to identify the most relevant genetic variations underlying a pat
Autor:
Marilyn Safran, Doron Lancet, Tsippi Iny-Stein, Ofer Zelig, Yaron Mazor, Ruth Barshir, Simon Fishilevich, Yaron Guan-Golan
Publikováno v:
Journal of Molecular Biology. 433:166913
Non-coding RNA (ncRNA) genes assume increasing biological importance, with growing associations with diseases. Many ncRNA sources are transcript-centric, but for non-coding variant analysis and disease decipherment it is essential to transform this i
Autor:
Marilyn Safran, Doron Lancet, Yaron Guan-Golan, Tsippi Iny-Stein, Ofer Zelig, Ruth Barshir, Simon Fishilevich
Publikováno v:
Molecular Genetics and Metabolism. 132:S123