2,497 research outputs found
Information retrieval on urban affairs
Designing data acquisition and information retrieval system for urban affairs researc
Apparatus for use in the production of ribbon-shaped crystals from a silicon melt
A susceptor for facilitating induction heating of silicon melt is described. The susceptor comprises a pair of susceptor halves of a thickness less than two skin depths, each being the mirror image of the other, disposed in mutually opposed, electrically insulated relation. The crucible comprises a quartz body supported by the graphite susceptor, whereby the R-F coil is electrically coupled with the melt
Means for growing ribbon crystals without subjecting the crystals to thermal shock-induced strains
A susceptor particularly suited for use in growing a ribbon crystal employing edge defined film fed growth techniques is described. The susceptor includes a die through which a melt is drawn for forming a crystal ribbon. This is combined with a coolant delivery system characterized by a pair of jets for directing a stream of fluid coolant along a path extended to impinge on the susceptor in close proximity with the die in nonincident relation with the crystal being grown
New Algorithms for Position Heaps
We present several results about position heaps, a relatively new alternative
to suffix trees and suffix arrays. First, we show that, if we limit the maximum
length of patterns to be sought, then we can also limit the height of the heap
and reduce the worst-case cost of insertions and deletions. Second, we show how
to build a position heap in linear time independent of the size of the
alphabet. Third, we show how to augment a position heap such that it supports
access to the corresponding suffix array, and vice versa. Fourth, we introduce
a variant of a position heap that can be simulated efficiently by a compressed
suffix array with a linear number of extra bits
Finding Fault?: Exploring Legal Duties to Return Incidental Findings in Genomic Research
The use of whole genome sequencing in biomedical research is expected to produce dramatic advances in human health. The increasing use of this powerful, data-rich new technology in research, however, will inevitably give rise to incidental findings (IFs), findings with individual health or reproductive significance that are beyond the aims of the particular research, and the related questions of whether and to what extent researchers have an ethical obligation to return IFs. Many have concluded that researchers have an ethical obligation to return some findings in some circumstances, but have provided vague or context-dependent approaches to determining which IFs must be returned and when. As a result, researchers have started returning IFs inconsistently, giving rise to concerns about legal liability in circumstances in which notification could have potentially prevented injury. While it is clear that ethical guidance should not be automatically codified as the law, and that crafting ethical obligations around legal duties can be inappropriate, the ethical debate should not proceed unaware of the potential legal ramifications of advancing and implementing an ethical obligation to return IFs.
This article is the first to assess the legal claims that could be brought for a researcher’s failure to return IFs. The potential for researchers to be held liable in tort is still uncertain and turns largely on a number of factors — including customary practice and guidance documents — that are still in flux. Unlike medical care, which has a well-defined duty into which evolving scientific knowledge about genetics and genomics can readily be incorporated, a researcher’s duty to return IFs is less well defined, making it difficult to determine at the outset whether and when legal liability will attach.
This article advocates for a clearer, ethically sound standard of requiring that researchers disclose in the informed consent document which approach to offering IFs will be taken. This approach enables participants to know at the outset which findings will be returned, allows researchers to ascertain when their failure to appropriately return incidental findings will give rise to liability, and enables courts to make determinations that will produce consistent legal guidance
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The Non-Linear Risk of Mortality by Income Level in a Healthy Population: US National Health and Nutrition Examination Survey mortality Follow-up Cohort, 1988-2001
Background: An examination of where in the income distribution income is most strongly associated with risk of mortality will provide guidance for identifying the most critical pathways underlying the connections between income and mortality, and may help to inform public health interventions to reduce socioeconomic disparities. Prior studies have suggested stronger associations at the lower end of the income distribution, but these studies did not have detailed categories of income, were unable to exclude individuals whose declining health may affect their income and did not use methods to determine exact threshold points of non-linearity. The purpose of this study is to describe the non-linear risks of all-cause and cause-specific mortality across the income distribution. Methods: We examined potential non-linear risk of mortality by family income level in a population that had not retired early, changed jobs, or changed to part-time work due to health reasons, in order to minimize the effects of illness on income. We used data from the US National Health and Nutrition Examination Survey (1988–1994), among individuals age 18–64 at baseline, with mortality follow-up to the year 2001 (ages 25–77 at the end of follow-up, 106 037 person-years of time at risk). Differential risk of mortality was examined using proportional hazard models with penalized regression splines in order to allow for non-linear associations between mortality risk and income, controlling for age, race/ethnicity, marital status, level of educational attainment and occupational category. Results: We observed significant non-linear risks of all-cause mortality, as well as for certain specific causes of death at different levels of income. Typically, risk of mortality decreased with increasing income levels only among persons whose family income was below the median; above this level, there was little decreasing risk of mortality with higher levels of income. There was also some variation in mortality risk at different levels of income by cause and gender. Conclusion: The majority of the income associated mortality risk in individuals between the ages of 18–77 in the United States is among the population whose family income is below the median (equal to $20,190 in 1991, 3.2 times the poverty level). Efforts to decrease socioeconomic disparities may have the greatest impact if focused on this population
Ethics of Genetic and Biomarker Test Disclosures in Neurodegenerative Disease Prevention Trials
OBJECTIVE:
Prevention trials for neurodegenerative diseases use genetic or other risk marker tests to select participants but there is concern that this could involve coercive disclosure of unwanted information. This has led some trials to use blinded enrollment (participants are tested but not told of their risk marker status). We examined the ethics of blinded vs transparent enrollment using well-established criteria for assessing the ethics of clinical research.
METHODS:
Normative analysis applying 4 key ethical criteria-favorable risk-benefit ratio, informed consent, fair subject selection, and scientific validity-to blinded vs transparent enrollment, using current evidence and state of Alzheimer disease (AD) and other prevention trials.
RESULTS:
Current evidence on the psychosocial impact of risk marker disclosure and considerations of scientific benefit do not support an obligation to use blinded enrollment in prevention trials. Nor does transparent enrollment coerce or involve undue influence of potential participants. Transparent enrollment does not unfairly exploit vulnerable participants or limit generalizability of scientific findings of prevention trials. However, if the preferences of a community of potential participants would affect the rigor or feasibility of a prevention trial using transparent enrollment, then investigators are required by considerations of scientific validity to use blinded enrollment.
CONCLUSIONS:
Considerations of risks and benefits, informed consent, and fair subject selection do not require the use of blinded enrollment for AD prevention trials. Blinded enrollment in AD prevention trials may sometimes be necessary because of the need for scientific validity, not because it prevents coercion or undue influence
One-variable word equations in linear time
In this paper we consider word equations with one variable (and arbitrary
many appearances of it). A recent technique of recompression, which is
applicable to general word equations, is shown to be suitable also in this
case. While in general case it is non-deterministic, it determinises in case of
one variable and the obtained running time is O(n + #_X log n), where #_X is
the number of appearances of the variable in the equation. This matches the
previously-best algorithm due to D\k{a}browski and Plandowski. Then, using a
couple of heuristics as well as more detailed time analysis the running time is
lowered to O(n) in RAM model. Unfortunately no new properties of solutions are
shown.Comment: submitted to a journal, general overhaul over the previous versio
Using Specialist Screening Practitioners (SSPs) to increase uptake of the Bowel Scope (Flexible Sigmoidoscopy) Screening Programme: a study protocol for a feasibility single stage phase II trial
The NHS Bowel Scope Screening (BSS) programme offers men and women aged 55 years a once-only flexible sigmoidoscopy (FS), a test that can help reduce colorectal cancer (CRC) incidence and mortality. However, the benefits of BSS are contingent on uptake. This NIHR funded single-stage phase II trial will test the feasibility of using Patient Navigation (PN), an intervention that offers support to patients to overcome barriers to healthcare, to increase BSS uptake within a socially deprived area of England
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