455 research outputs found
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Noise-Aware Inference for Differential Privacy
Domains involving sensitive human data, such as health care, human mobility, and online activity, are becoming increasingly dependent upon machine learning algorithms. This leads to scenarios in which data owners wish to protect the privacy of individuals comprising the sensitive data, while at the same time data modelers wish to analyze and draw conclusions from the data. Thus there is a growing demand to develop effective private inference methods that can marry the needs of both parties. For this we turn to differential privacy, which provides a framework for executing algorithms in a private fashion by injecting specifically-designed randomization at various points in the process. The majority of existing work proceeds by ignoring the injected randomization, potentially leading to pathologies in algorithmic performance. There is, however, a small body of existing work that performs inference over the injected randomization in an attempt to design more principled algorithms. This thesis summarizes the subfield of noise-aware differentially private inference and contributes novel algorithms for important problems.
Differential privacy literature provides a multitude of privacy mechanisms. We opt for sufficient statistics perturbation (SSP), in which sufficient statistics, a quantity that captures all information about the model parameters, are corrupted with random noise and released to the public. This mechanism offers desirable efficiency properties in comparison to alternatives. In this thesis we develop methods in a principled manner that directly accounts for the injected noise in three settings: maximum likelihood estimation of undirected graphical models, Bayesian inference of exponential family models, and Bayesian inference of conditional regression models
Improved Parameters and New Lensed Features for Q0957+561 from WFPC2 Imaging
New HST WFPC2 observations of the lensed double QSO 0957+561 will allow
improved constraints on the lens mass distribution and hence will improve the
derived value of H. We first present improved optical positions and
photometry for the known components of this lens. The optical separation
between the A and B quasar images agrees with VLBI data at the 10 mas level,
and the optical center of the primary lensing galaxy G1 coincides with the VLBI
source G' to within 10 mas. The best previous model for this lens (Grogin and
Narayan 1996) is excluded by these data and must be reevaluated.
Several new resolved features are found within 10\arcsec of G1, including an
apparent fold arc with two bright knots. Several other small galaxies are
detected, including two which may be multiple images of each other. We present
positions and crude photometry of these objects.Comment: 7 pages including 2 postscript figures, LaTeX, emulateapj style. Also
available at
http://www.astro.lsa.umich.edu:80/users/philf/www/papers/list.htm
Values of H_0 from Models of the Gravitational Lens 0957+561
The lensed double QSO 0957+561 has a well-measured time delay and hence is
useful for a global determination of H0. Uncertainty in the mass distribution
of the lens is the largest source of uncertainty in the derived H0. We
investigate the range of \hn produced by a set of lens models intended to mimic
the full range of astrophysically plausible mass distributions, using as
constraints the numerous multiply-imaged sources which have been detected. We
obtain the first adequate fit to all the observations, but only if we include
effects from the galaxy cluster beyond a constant local magnification and
shear. Both the lens galaxy and the surrounding cluster must depart from
circular symmetry as well.
Lens models which are consistent with observations to 95% CL indicate
H0=104^{+31}_{-23}(1-\kthirty) km/s/Mpc. Previous weak lensing measurements
constrain the mean mass density within 30" of G1 to be kthirty=0.26+/-0.16 (95%
CL), implying H0=77^{+29}_{-24}km/s/Mpc (95% CL). The best-fitting models span
the range 65--80 km/s/Mpc. Further observations will shrink the confidence
interval for both the mass model and \kthirty.
The range of H0 allowed by the full gamut of our lens models is substantially
larger than that implied by limiting consideration to simple power law density
profiles. We therefore caution against use of simple isothermal or power-law
mass models in the derivation of H0 from other time-delay systems. High-S/N
imaging of multiple or extended lensed features will greatly reduce the H0
uncertainties when fitting complex models to time-delay lenses.Comment: AASTEX, 48 pages 4 figures, 2 tables. Also available at:
http://www.astro.lsa.umich.edu:80/users/philf/www/papers/list.htm
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Injectable diblock copolypeptide hydrogel provides platform to maintain high local concentrations of taxol and local tumor control
Abstract Introduction Surgical resection and systemic chemotherapy with temozolomide remain the mainstay for treatment of glioblastoma. However, many patients are not candidates for surgical resection given inaccessible tumor location or poor health status. Furthermore, despite being first line treatment, temozolomide has only limited efficacy. Methods The development of injectable hydrogel-based carrier systems allows for the delivery of a wide range of chemotherapeutics that can achieve high local concentrations, thus potentially avoiding systemic side effects and wide-spread neurotoxicity. To test this modality in a realistic environment, we developed a diblock copolypeptide hydrogel (DCH) capable of carrying and releasing paclitaxel, a compound that we found to be highly potent against primary gliomasphere cells. Results The DCH produced minimal tissue reactivity and was well tolerated in the immune-competent mouse brain. Paclitaxel-loaded hydrogel induced less tissue damage, cellular inflammation and reactive astrocytes than cremaphor-taxol (typical taxol-carrier) or hydrogel alone. In a deep subcortical xenograft model, of glioblastoma in immunodeficient mice, injection of paclitaxel-loaded hydrogel led to a high local concentration of paclitaxel and led to local tumor control and improved survival. However, the tumor cells were highly migratory and were able to eventually escape the area of treatment. Conclusions These findings suggest this technology may be ultimately applicable to patients with deep-seated inoperable tumors, but as currently formulated, complete tumor eradication would be highly unlikely. Future studies should focus on targeting the migratory potential of surviving cells
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