Christine Ho
University of California, Berkeley
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Publication
Featured researches published by Christine Ho.
advanced information networking and applications | 2007
C.R. Baker; K. Armijo; S. Belka; M. Benhabib; V. Bhargava; N. Burkhart; A. Der Minassians; G. Dervisoglu; L. Gutnik; M.B. Haick; Christine Ho; M. Koplow; Jennifer Mangold; Stefanie Robinson; M. Rosa; M. Schwartz; Christo Sims; H. Stoffregen; Andrew Waterbury; Eli S. Leland; Trevor Pering; Paul K. Wright
Sophisticated electronics are within reach of average users. Cooperation between wireless sensor networks and existing consumer electronic infrastructures can assist in the areas of health care and patient monitoring. This will improve the quality of life of patients, provide early detection for certain ailments, and improve doctor-patient efficiency. The goal of our work is to focus on health-related applications of wireless sensor networks. In this paper we detail our experiences building several prototypes and discuss the driving force behind home health monitoring and how current (and future) technologies will enable automated home health monitoring.
Cancer Discovery | 2011
Steffen Durinck; Christine Ho; Nicholas Wang; Wilson Liao; Lakshmi Jakkula; Eric A. Collisson; Jennifer Pons; Sai Wing Chan; Ernest T. Lam; Catherine Chu; Kyung-Hee Park; Sungwoo Hong; Joe S Hur; Nam Huh; Isaac M. Neuhaus; Siegrid S. Yu; Roy C. Grekin; Theodora M. Mauro; James E. Cleaver; Pui-Yan Kwok; Philip E. LeBoit; Gad Getz; Kristian Cibulskis; Haiyan Huang; Elizabeth Purdom; Jian Li; Lars Bolund; Sarah T. Arron; Joe W. Gray; Paul T. Spellman
Timely intervention for cancer requires knowledge of its earliest genetic aberrations. Sequencing of tumors and their metastases reveals numerous abnormalities occurring late in progression. A means to temporally order aberrations in a single cancer, rather than inferring them from serially acquired samples, would define changes preceding even clinically evident disease. We integrate DNA sequence and copy number information to reconstruct the order of abnormalities as individual tumors evolve for 2 separate cancer types. We detect vast, unreported expansion of simple mutations sharply demarcated by recombinative loss of the second copy of TP53 in cutaneous squamous cell carcinomas (cSCC) and serous ovarian adenocarcinomas, in the former surpassing 50 mutations per megabase. In cSCCs, we also report diverse secondary mutations in known and novel oncogenic pathways, illustrating how such expanded mutagenesis directly promotes malignant progression. These results reframe paradigms in which TP53 mutation is required later, to bypass senescence induced by driver oncogenes.
Lancet Infectious Diseases | 2006
Maninder Singh Setia; Craig Steinmaus; Christine Ho; George W. Rutherford
The present meta-analysis investigates the role of BCG-a widely used yet controversial vaccine-in the prevention of leprosy. The electronic databases Medline, Embase, the Cochrane Library, and LILACS were searched to identify studies assessing the protective effect of BCG against leprosy. We included seven experimental studies and 19 observational studies. The experimental studies demonstrated an overall protective effect of 26% (95% CI 14-37%). At 61% (95% CI 51-70%), the observational studies overestimated the protective effect. The age at vaccination did not predict the protective effect of BCG. An additional dose of BCG was more protective in the prevention of leprosy compared with a single dose. An additional dose of BCG may be warranted for contacts of leprosy patients in areas where leprosy continues to be a public-health problem.
Tropical Medicine & International Health | 2006
Shriprakash Kalantri; Amandeep Singh; Rajnish Joshi; Samuel Malamba; Christine Ho; Joseph Ezoua; Maureen Morgan
Objective To determine the association between selected admission risk factors and in‐hospital mortality in patients admitted with venomous snake bite to a rural tertiary care hospital in central India.
Bioinformatics | 2013
Elizabeth Purdom; Christine Ho; Catherine S. Grasso; Michael J. Quist; Raymond J. Cho; Paul T. Spellman
Motivation: Tumors acquire many chromosomal amplifications, and those acquired early in the lifespan of the tumor may be not only important for tumor growth but also can be used for diagnostic purposes. Many methods infer the order of the accumulation of abnormalities based on their occurrence in a large cohort of patients. Recently, Durinck et al. (2011) and Greenman et al. (2012) developed methods to order a single tumor’s chromosomal amplifications based on the patterns of mutations accumulated within those regions. This method offers an unprecedented opportunity to assess the etiology of a single tumor sample, but has not been widely evaluated. Results: We show that the model for timing chromosomal amplifications is limited in scope, particularly for regions with high levels of amplification. We also show that the estimation of the order of events can be sensitive for events that occur early in the progression of the tumor and that the partial maximum likelihood method of Greenman et al. (2012) can give biased estimates, particularly for moderate read coverage or normal contamination. We propose a maximum-likelihood estimation procedure that fully accounts for sequencing variability and show that it outperforms the partial maximum-likelihood estimation method. We also propose a Bayesian estimation procedure that stabilizes the estimates in certain settings. We implement these methods on a small number of ovarian tumors, and the results suggest possible differences in how the tumors acquired amplifications. Availability and implementation: We provide implementation of these methods in an R package cancerTiming, which is available from the Comprehensive R Archive Network (CRAN) at http://CRAN.R-project.org/. Contact: [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
wearable and implantable body sensor networks | 2009
Christine Ho; Michael Mark; Michael Koplow; Lindsay M. Miller; Alic Chen; Elizabeth K. Reilly; Jan M. Rabaey; James W. Evans; Paul K. Wright
We present a design study highlighting our recent technological developments that will enable the implementation of autonomous wireless sensor networks for home healthcare monitoring systems. We outline the power requirements for a commercially available implantable glucose sensor which transmits measurements to an external wireless sensor node embedded in the home. A network of these sensor nodes will relay the data to a base station, such as a computer with internet connection, which will record and report this data to the user. We explore the feasibility of powering these sensors using energy scavenging from both body temperature gradients and vibrations in the home, and discuss our developments in energy storage and low power consuming hardware.
Archive | 2013
Paul K. Wright; James W. Evans; Christine Ho
208th ECS Meeting | 2006
Daniel A. Steingart; Andrew Redfern; Christine Ho; Paul K. Wright; James W. Evans
Archive | 2012
Adam G. Kirk; Christine Ho; Alejandro de la Fuente Vornbrock; David Garmire
Archive | 2007
Daniel A. Steingart; Andrew Redfern; Christine Ho; C. S. Kumai; James W. Evans