Gait recognition using normalized shadows

WOS:000426986000189 (Nº de Acesso Web of Science)Surveillance of public spaces is often conducted with the help of cameras placed at elevated positions. Recently, drones with high resolution cameras have made it possible to perform overhead surveillance of critical spaces. However, images obtained in these conditions may not contain enough body features to allow conventional biometric recognition. This paper introduces a novel gait recognition system which uses the shadows cast by users, when available. It includes two main contributions: (i) a method for shadow segmentation, which analyzes the orientation of the silhouette contour to identify the feet position along time, in order to separate the body and shadow silhouettes connected at such positions; (ii) a method that normalizes the segmented shadow silhouettes, by applying a transformation derived from optimizing the low rank textures of a gait texture image, to compensate for changes in view and shadow orientation. The normalized shadow silhouettes can then undergo a gait recognition algorithm, which in this paper relies on the computation of a gait energy image, combined with linear discriminant analysis for user recognition. The proposed system outperforms the available state-of-the-art, being robust to changes in acquisition viewpoints.info:eu-repo/semantics/acceptedVersio

Fractal aggregation kinetics contributions to thermal conductivity of nano-suspensions in unsteady thermal convection

Nano-suspensions (NS) exhibit unusual thermophysical behaviors once interparticle aggregations and the shear flows are imposed, which occur ubiquitously in applications but remain poorly understood, because existing theories have not paid these attentions but focused mainly on stationary NS. Here we report the critical role of time-dependent fractal aggregation in the unsteady thermal convection of NS systematically. Interestingly, a time ratio λ = t(p)/t(m) (t(p) is the aggregate characteristic time, t(m) the mean convection time) is introduced to characterize the slow and fast aggregations, which affect distinctly the thermal convection process over time. The increase of fractal dimension reduces both momentum and thermal boundary layers, meanwhile extends the time duration for the full development of thermal convection. We find a nonlinear growth relation of the momentum layer, but a linear one of the thermal layer, with the increase of primary volume fraction of nanoparticles for different fractal dimensions. We present two global fractal scaling formulas to describe these two distinct relations properly, respectively. Our theories and methods in this study provide new evidence for understanding shear-flow and anomalous heat transfer of NS associated non-equilibrium aggregation processes by fractal laws, moreover, applications in modern micro-flow technology in nanodevices

Pengembangan Media Pembelajaran Fisika Berupa Buletin Dalam Bentuk Buku Saku Untuk Pembelajaran Fisikakelas VIII Materi Gaya Ditinjau Dari Minat Baca Siswa

Tujuan dari penelitian ini untuk mengembangkan media pembelajaran berupa buletin dalam bentuk buku saku untuk pembelajaran Fisika kelas VIII pada materi Gaya ditinjau dari aspek materi, konstruk, dan bahasa serta minat baca siswa. Penelitian ini termasuk penelitian pengembangan yang menggunakan metode Research and Development (R&D). Penelitian ini menggunakan model pengembangan model prosedural yaitu model yang bersifat deskriptif yang menunjukkan tahapan-tahapan yang harus diikuti untuk menghasilkan produk berupa media pembelajaran.Jenis data yang diperoleh bersifat kualitatif dan kuantitatif yaitu angket dan wawancara. Teknik analisis data yang digunakan adalah analisis deskriptif kualitatif dan kuantitatif. Hasil penelitian menunjukkan bahwa media pembelajaran yang dikembangkan berupa buletin Fisika dalam bentuk buku saku memiliki kriteria sangat baik berdasarkan penilaian dari ahli materi, ahli bahasa Indonesia, dan ahli media memberikan rata-rata penilaian sebesar 86,56%. Media pembelajaran yang dikembangkan juga memiliki kriteria sangat baik bila ditinjau dari peningkatan minat baca siswa. Hal ini terbukti pada hasil angket minat baca awal dan akhir yang diberikan kepada siswa yang memberikan rata-rata peningkatan sebesar 11,13%. Selain itu juga dianalisis dengan menggunakan uji-t berpasangan terhadap data masing-masing kelompok uji coba untuk mengetahui signifikansi dari peningkatan minat baca siswa. Untuk uji coba perorangan diperoleh hasil perhitungan thitung = 6,957 > ttabel = 1,943 dan nilai Sig. = 0,001 < 0,05 yang berarti sangat signifikan. Untuk kelompok kecil didapatkan hasil perhitungan bahwa thitung = 7,848 > ttabel = 1,725 dan nilai Sig. = 0,000 < 0,05 yang berarti sangat signifikan. Untuk kelompok besar juga didapatkan hasil perhitungan bahwa thitung = 20,214 > ttabel = 1,725 dan nilai Sig. = 0,000 < 0,05 yang berarti sangat signifikan. Simpulan dari penelitian ini adalah media pembelajaran berupa buletin dalam bentuk buku saku memiliki kriteria sangat baik bila ditinjau dari aspek materi, konstruk, dan bahasa serta minat baca siswa

The DNA Repair Gene APE1 T1349G Polymorphism and Risk of Gastric Cancer in a Chinese Population

Background: Apurinic/apyrimidinic endonuclease 1 (APE1) has a central role in the repair of apurinic apyrimidic sites through both its endonuclease and its phosphodiesterase activities. A common APE1 polymorphism, T1349G (rs3136820), was previously shown to be associated with the risk of cancers. Objective: We hypothesized that the APE1 T1349G polymorphism is also associated with risk of gastric cancer. Methods: In a hospital-based case-control study of 338 case patients with newly diagnosed gastric cancer and 362 cancerfree controls frequency-matched by age and sex, we genotyped the T1349G polymorphism and assessed its associations with risk of gastric cancer. Results: Compared with the APE1 TT genotype, individuals with the variant TG/GG genotypes had a significantly increased risk of gastric cancer (odds ratio = 1.69, 95 % confidence interval = 1.19–2.40), which was more pronounced among subgroups of aged #60 years, male, ever smokers, and ever drinkers. Further analyses revealed that the variant genotypes were associated with an increased risk for diffuse-type, low depth of tumor infiltration (T1 and T2), and lymph node metastasis gastric cancer. Conclusions: The APE1 T1349G polymorphism may be a marker for the development of gastric cancer in the Chinese population. Larger studies are required to validate these findings in diverse populations

Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects

The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have congenital heart disease, mostly of the conotruncal type (CTD), whereas others have normal cardiac anatomy. In this study, we tested whether variants in the hemizygous LCR22A-D region are associated with risk for CTDs on the basis of the sequence of the 22q11.2 region from 1,053 22q11.2DS individuals. We found a significant association (FDR p < 0.05) of the CTD subset with 62 common variants in a single linkage disequilibrium (LD) block in a 350 kb interval harboring CRKL. A total of 45 of the 62 variants were associated with increased risk for CTDs (odds ratio [OR) ranges: 1.64-4.75). Associations of four variants were replicated in a meta-analysis of three genome-wide association studies of CTDs in affected individuals without 22q11.2DS. One of the replicated variants, rs178252, is located in an open chromatin region and resides in the double-elite enhancer, GH22J020947, that is predicted to regulate CRKL (CRK-like proto-oncogene, cytoplasmic adaptor) expression. Approximately 23% of patients with nested LCR22C-D deletions have CTDs, and inactivation of Crkl in mice causes CTDs, thus implicating this gene as a modifier. Rs178252 and rs6004160 are expression quantitative trait loci (eQTLs) of CRKL. Furthermore, set-based tests identified an enhancer that is predicted to target CRKL and is significantly associated with CTD risk (GH22J020946, sequence kernal association test (SKAT) p = 7.21 × 10-5) in the 22q11.2DS cohort. These findings suggest that variance in CTD penetrance in the 22q11.2DS population can be explained in part by variants affecting CRKL expression

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in addition to the ~20-fold increased risk conveyed by the 22q11.2 deletion. Using whole-genome sequencing data from 519 unrelated individuals with 22q11.2DS, we conducted genome-wide comparisons of common and rare variants between those with schizophrenia and those with no psychotic disorder at age ≥25 years. Available microarray data enabled direct comparison of polygenic risk for schizophrenia between 22q11.2DS and independent population samples with no 22q11.2 deletion, with and without schizophrenia (total n = 35,182). Polygenic risk for schizophrenia within 22q11.2DS was significantly greater for those with schizophrenia (padj = 6.73 × 10−6). Novel reciprocal case–control comparisons between the 22q11.2DS and population-based cohorts showed that polygenic risk score was significantly greater in individuals with psychotic illness, regardless of the presence of the 22q11.2 deletion. Within the 22q11.2DS cohort, results of gene-set analyses showed some support for rare variants affecting synaptic genes. No common or rare variants within the 22q11.2 deletion region were significantly associated with schizophrenia. These findings suggest that in addition to the deletion conferring a greatly increased risk to schizophrenia, the risk is higher when the 22q11.2 deletion and common polygenic risk factors that contribute to schizophrenia in the general population are both present