4,857 research outputs found
Automated legal sensemaking: the centrality of relevance and intentionality
Introduction: In a perfect world, discovery would ideally be conducted by the senior litigator who is
responsible for developing and fully understanding all nuances of their clientâs legal strategy. Of
course today we must deal with the explosion of electronically stored information (ESI) that
never is less than tens-of-thousands of documents in small cases and now increasingly involves
multi-million-document populations for internal corporate investigations and litigations.
Therefore scalable processes and technologies are required as a substitute for the authorityâs
judgment. The approaches taken have typically either substituted large teams of surrogate
human reviewers using vastly simplified issue coding reference materials or employed
increasingly sophisticated computational resources with little focus on quality metrics to insure
retrieval consistent with the legal goal. What is required is a system (people, process, and
technology) that replicates and automates the senior litigatorâs human judgment.
In this paper we utilize 15 years of sensemaking research to establish the minimum acceptable
basis for conducting a document review that meets the needs of a legal proceeding. There is
no substitute for a rigorous characterization of the explicit and tacit goals of the senior litigator.
Once a process has been established for capturing the authorityâs relevance criteria, we argue
that literal translation of requirements into technical specifications does not properly account for
the activities or states-of-affairs of interest. Having only a data warehouse of written records, it
is also necessary to discover the intentions of actors involved in textual communications. We
present quantitative results for a process and technology approach that automates effective
legal sensemaking
An unusual interplay among disorder, Kondo-effect and spin-glass behavior in the Kondo lattices, CeAuCoSi
We report the results of magnetic measurements for the solid solution
CeAuCoSi. The results reveal that this solid solution is
characterized by a magnetic phase diagram (plot of magnetic transition
temperature versus ) unusual for Kondo lattices. In particular, the
spin-glass freezing induced by disorder is observed only for the compositions
at the weak coupling limit; as one approaches the quantum critical point by a
gradual replacement of Au by Co, this disorder effect is surprisingly
suppressed in favor of long range antiferro-magnetic ordering in contrast to
expectations. This unusual interplay between disorder, spin-glass freezing and
the Kondo-effect calls for further refinement of theories on competition
between magnetism and the Kondo effect.Comment: 4 pages, 3 figure
New Constraints on the Origin of the Short-Term Cyclical Variability of the Wolf-Rayet Star WR 46
The Wolf-Rayet star WR 46 is known to exhibit a very complex variability
pattern on relatively short time scales of a few hours. Periodic but
intermittent radial velocity shifts of optical lines as well as multiple
photometric periods have been found in the past. Non-radial pulsations, rapid
rotational modulation or the presence of a putative low-mass companion have
been proposed to explain the short-term behaviour. In an effort to unveil its
true nature, we observed WR 46 with FUSE (Far Ultraviolet Spectroscopic
Explorer) over several short-term variability cycles. We found significant
variations on a time scale of ~8 hours in the far-ultraviolet (FUV) continuum,
in the blue edge of the absorption trough of the OVI {\lambda}{\lambda}1032,
1038 doublet P Cygni profile and in the SVI {\lambda}{\lambda}933, 944 P Cygni
absorption profile. We complemented these observations with X-ray and UV
light-curves and an X-ray spectrum from archival XMM-Newton (X-ray Multi-Mirror
Mission - Newton Space Telescope) data. The X-ray and UV light-curves show
variations on a time scale similar to the variability found in the FUV. We
discuss our results in the context of the different scenarios suggested to
explain the short-term variability of this object and reiterate that non-radial
pulsations is the most likely to occur.Comment: 36 pages, 11 figures. Accepted for publication in Ap
On the Kernel of -Linear Hadamard Codes
The -additive codes are subgroups of ,
and can be seen as a generalization of linear codes over and
. A -linear Hadamard code is a binary Hadamard
code which is the Gray map image of a -additive code. It is
known that the dimension of the kernel can be used to give a complete
classification of the -linear Hadamard codes. In this paper, the
kernel of -linear Hadamard codes and its dimension are
established for . Moreover, we prove that this invariant only provides a
complete classification for some values of and . The exact amount of
nonequivalent such codes are given up to for any , by using
also the rank and, in some cases, further computations
Crying and feeding problems in infancy and cognitive outcome in preschool children born at risk : a prospective population study
Objective: To investigate whether regulatory problems, i.e., crying and feeding problems in infants > 3 months of age, predict cognitive outcome in preschool children born at risk even when controlled for confounding factors.
Methods: A prospective longitudinal study of children born in a geographically defined area in Germany. N = 4427 children of 6705 eligible survivors (66%) participated at all four assessment points (neonatal, 5, 20, and 56 months of age). Excessive crying and feeding problems were measured at 5 months. Mental development was assessed with the Griffiths Scale at 20 months, and cognitive assessments were conducted at 56 months. Neonatal complications, neurological, and psychosocial factors were controlled as confounders in structural equation modeling and analyses of variance.
Results: One in five infants suffered from single crying or feeding problems, and 2% had multiple regulatory problems, i.e., combined crying and feeding problems at 5 months. In girls, regulatory problems were directly predictive of lower cognition at 56 months, even when controlled for confounders, whereas in boys, the influence on cognition at 56 months was mediated by low mental development at 20 months. Both in boys and girls, shortened gestational age, neonatal neurological complications, and poor parent-infant relationship were predictive of regulatory problems at 5 months and lower cognition at 56 months.
Conclusion: Regulatory problems in infancy have a small but significant adverse effect on cognitive development
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
OBJECTIVE: To identify factors that determine disease severity and clinical
phenotype of the most common spinocerebellar ataxias (SCAs), we studied 526
patients with SCA1, SCA2, SCA3. or SCA6.
METHODS: To measure the severity of ataxia we used the Scale for the Assessment
and Rating of Ataxia (SARA). In addition, nonataxia symptoms were assessed with
the Inventory of Non-Ataxia Symptoms (INAS). The INAS count denotes the number of
nonataxia symptoms in each patient.
RESULTS: An analysis of covariance with SARA score as dependent variable and
repeat lengths of the expanded and normal allele, age at onset, and disease
duration as independent variables led to multivariate models that explained 60.4%
of the SARA score variance in SCA1, 45.4% in SCA2, 46.8% in SCA3, and 33.7% in
SCA6. In SCA1, SCA2, and SCA3, SARA was mainly determined by repeat length of the
expanded allele, age at onset, and disease duration. The only factors determining
the SARA score in SCA6 were age at onset and disease duration. The INAS count was
5.0 +/- 2.3 in SCA1, 4.6 +/- 2.2 in SCA2, 5.2 +/- 2.5 in SCA3, and 2.0 +/- 1.7 in
SCA6. In SCA1, SCA2, and SCA3, SARA score and disease duration were the strongest
predictors of the INAS count. In SCA6, only age at onset and disease duration had
an effect on the INAS count.
CONCLUSIONS: Our study suggests that spinocerebellar ataxia (SCA) 1, SCA2, and
SCA3 share a number of common biologic properties, whereas SCA6 is distinct in
that its phenotype is more determined by age than by disease-related factors
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