Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Uma S Mudunuri"'
Autor:
Albino Bacolla, Nuri A Temiz, Ming Yi, Joseph Ivanic, Regina Z Cer, Duncan E Donohue, Edward V Ball, Uma S Mudunuri, Guliang Wang, Aklank Jain, Natalia Volfovsky, Brian T Luke, Robert M Stephens, David N Cooper, Jack R Collins, Karen M Vasquez
Publikováno v:
PLoS Genetics, Vol 9, Iss 9, p e1003816 (2013)
Single base substitutions constitute the most frequent type of human gene mutation and are a leading cause of cancer and inherited disease. These alterations occur non-randomly in DNA, being strongly influenced by the local nucleotide sequence contex
Externí odkaz:
https://doaj.org/article/14b860078cfe45a0be15900a05064fcf
Autor:
Uma S Mudunuri, Mohamad Khouja, Stephen Repetski, Girish Venkataraman, Anney Che, Brian T Luke, F Pascal Girard, Robert M Stephens
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e80503 (2013)
As the discipline of biomedical science continues to apply new technologies capable of producing unprecedented volumes of noisy and complex biological data, it has become evident that available methods for deriving meaningful information from such da
Externí odkaz:
https://doaj.org/article/33001faaa4b54d748669906208c339c5
Autor:
Erica L. Lyons, Daniel Watson, Mohammad S. Alodadi, Sharie J. Haugabook, Gregory J. Tawa, Fady Hannah-Shmouni, Forbes D. Porter, Jack R. Collins, Elizabeth A. Ottinger, Uma S. Mudunuri
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-18 (2023)
Abstract Background Approximately 4–8% of the world suffers from a rare disease. Rare diseases are often difficult to diagnose, and many do not have approved therapies. Genetic sequencing has the potential to shorten the current diagnostic process,
Externí odkaz:
https://doaj.org/article/e690a548a1d4449da411eb08d584528a