Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Eishita Tyagi"'
Autor:
Lavanya Rishishwar, Neha Varghese, Eishita Tyagi, Stephen C Harvey, I King Jordan, Nael A McCarty
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42336 (2012)
Cystic fibrosis (CF) is the most common genetic disease among Caucasians, and accordingly the cystic fibrosis transmembrane conductance regulator (CFTR) protein has perhaps the best characterized disease mutation spectrum with more than 1,500 causati
Externí odkaz:
https://doaj.org/article/e8045f77cb544b0abcb2634f4bed99df
Autor:
Ahsan Huda, Eishita Tyagi, Leonardo Mariño-Ramírez, Nathan J Bowen, Daudi Jjingo, I King Jordan
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27513 (2011)
Experimentally characterized enhancer regions have previously been shown to display specific patterns of enrichment for several different histone modifications. We modelled these enhancer chromatin profiles in the human genome and used them to guide
Externí odkaz:
https://doaj.org/article/147dc18a8fff4fecb434fe18fa2d5b50
There is a need for a comprehensive and sensitive method to test for a broad range of viral pathogens in samples without any identifiable pathogen detected. Real-time PCR assays are sensitive and rapid, but their specificity limits their utility in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b955c2325aee0ebb64f8c037048abda
https://doi.org/10.1101/2020.06.10.145052
https://doi.org/10.1101/2020.06.10.145052
Publikováno v:
Online Journal of Public Health Informatics
Developing a modular approach to infectious disease genomic analysis that can easily integrate with public health analytics systems. Using dynamic approaches to genomic sequence analysis, relevant whole genome data can be quickly and accurately visua
Autor:
Neha Varghese, Stephen C. Harvey, Nael A. McCarty, I. King Jordan, Lavanya Rishishwar, Eishita Tyagi
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42336 (2012)
PLoS ONE
PLoS ONE
Cystic fibrosis (CF) is the most common genetic disease among Caucasians, and accordingly the cystic fibrosis transmembrane conductance regulator (CFTR) protein has perhaps the best characterized disease mutation spectrum with more than 1,500 causati
Autor:
I. King Jordan, Daudi Jjingo, Leonardo Mariño-Ramírez, Eishita Tyagi, Ahsan Huda, Nathan J. Bowen
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27513 (2011)
PLoS ONE
PLoS ONE
Experimentally characterized enhancer regions have previously been shown to display specific patterns of enrichment for several different histone modifications. We modelled these enhancer chromatin profiles in the human genome and used them to guide