Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Diana Rush"'
Autor:
Hui Yang, Guillermo Garcia-Manero, Koji Sasaki, Guillermo Montalban-Bravo, Zhenya Tang, Yue Wei, Tapan Kadia, Kelly Chien, Diana Rush, Ha Nguyen, Awdesh Kalia, Manjunath Nimmakayalu, Carlos Bueso-Ramos, Hagop Kantarjian, L. Jeffrey Medeiros, Rajyalakshmi Luthra, Rashmi Kanagal-Shamanna
Publikováno v:
Leukemia. 36:2306-2316
Chromosome banding analysis (CBA) remains the standard-of-care for structural variant (SV) assessment in MDS. Optical genome mapping (OGM) is a novel, non-sequencing-based technique for high-resolution genome-wide SV profiling (SVP). We explored the
Autor:
Ha Nguyen, Sherin Raju, Nazneen Ahmed, Diana Rush, Mark Dubina, Hector Alvarez, Anthony San Lucas, Zhenya Tang, Bedia Barkoh, Hyvan Dang, James Ozenci, Simi Puthooran, Peter Hu, Awdhesh Kalia, Christopher Bowman, Luthra Rajyalakshmi, Rashmi Kanagal-Shamanna
Publikováno v:
Cancer Genetics. :2
Autor:
L. Jeffrey Medeiros, Saradhi Mallampati, Guillermo Montalban-Bravo, Rajyalakshmi Luthra, Guillermo Garcia-Manero, Diana Rush, Brynn Levy, Rashmi Kanagal-Shamanna, Hui Yang
Structural chromosomal variants [copy number variants (CNVs): losses/ gains and structural variants (SVs): inversions, balanced and unbalanced fusions/translocations] are important for diagnosis and risk-stratification of myelodysplastic syndromes (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f367f38b59e3c858ca359711df7b931
https://doi.org/10.1101/2021.01.13.21249611
https://doi.org/10.1101/2021.01.13.21249611
Autor:
Hui Yang, Guillermo Garcia-Manero, Diana Rush, Guillermo Montalban-Bravo, Saradhi Mallampati, Rajyalakshmi Luthra, Rashmi Kanagal-Shamanna
Publikováno v:
Cancer Genetics. :4
Autor:
Guillermo Garcia-Manero, Zhenya Tang, Kelly S. Chien, Awdesh Kalia, Diana Rush, Hagop M. Kantarjian, Yue Wei, Rashmi Kanagal-Shamanna, Manjunath Nimmakayalu, Rajyalakshmi Luthra, Hui Yang, L. Jeffrey Medeiros, Saradhi Mallampati, Guillermo Montalban-Bravo
Publikováno v:
Blood. 138:105-105
Introduction Introduction of next-generation sequencing has defined the somatic mutational landscape in MDS. Comprehensive high-throughput structural variant profiling (SVP) is as important as mutation profiling in characterizing MDS clonal architect