Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lukasz Kozon"'
Autor:
Ferrah London, Inessa Hakker, Peter Andrews, Vaidehi Jobanputra, Michael Ronemus, Kazimierz O. Wrzeszczynski, Lukasz Kozon, Avinash Abhyankar, Vanessa Felice, Dino Robinson
Publikováno v:
J Mol Diagn
Chromosomal microarray testing is indicated for patients with diagnoses including unexplained developmental delay or intellectual disability, autism spectrum disorders, and multiple congenital anomalies. The short multiply aggregated sequence homolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee2308a089c2f07f80ba193c36d4f58
https://doi.org/10.1016/j.jmoldx.2020.09.009
https://doi.org/10.1016/j.jmoldx.2020.09.009
Autor:
Xiaolan Fang, Dina Manaa, Olca Basturk, Umesh Bhanot, David Lin, Vanessa Felice, Govind Bhagat, Heather Geiger, Nicolas Robine, Michelle F. Lamendola-Essel, Kanika Arora, Ferrah London, Alex Kentsis, Anne-Katrin Emde, Esra Dikoglu, Kazimierz O. Wrzeszczynski, Mahesh M. Mansukhani, Depinder Khaira, Minita Shah, Vaidehi Jobanputra, Dino Robinson, Avinash Abhyankar, Lukasz Kozon
Publikováno v:
The Journal of Molecular Diagnostics : JMD
We developed and validated a clinical whole-genome and transcriptome sequencing (WGTS) assay that provides a comprehensive genomic profile of a patient's tumor. The ability to fully capture the mappable genome with sufficient sequencing coverage to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0c2ab11006fea092e09c572a0eb11b
https://pubmed.ncbi.nlm.nih.gov/30138725
https://pubmed.ncbi.nlm.nih.gov/30138725
Autor:
Kazimierz O. Wrzeszczynski, Govind Bhagat, Lukasz Kozon, Avinash Abhyankar, Olca Basturk, Anne-Katrin Emde, Umesh Bhanot, Nicolas Robine, Vanessa Felice, Alex Kentsis, Esra Dikoglu, Mahesh M. Mansukhani, Vaidehi Jobanputra
Publikováno v:
Cancer Research. 77:2714-2714
Next Generation DNA Sequencing (NGS) technologies are currently being applied in the clinical setting for the treatment of disease. The goal is to use high-throughput sequencing to identify specific variants within each tumor and recommend personaliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5111ca451412dd46dd3b8b8238715eb1
https://doi.org/10.1158/1538-7445.am2017-2714
https://doi.org/10.1158/1538-7445.am2017-2714