Adaptive Task Granularity Strategy for OpenMP3.0 Task Model on Cell Architecture

Author(s):  
Qian Cao ◽  
Changjun Hu ◽  
Shigang Li ◽  
Haohu He
Keyword(s):  
Author(s):  
Qing Liao ◽  
Heyan Chai ◽  
Hao Han ◽  
Xiang Zhang ◽  
Xuan Wang ◽  
...  
Keyword(s):  

Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 870
Author(s):  
Robby Neven ◽  
Toon Goedemé

Automating sheet steel visual inspection can improve quality and reduce costs during its production. While many manufacturers still rely on manual or traditional inspection methods, deep learning-based approaches have proven their efficiency. In this paper, we go beyond the state-of-the-art in this domain by proposing a multi-task model that performs both pixel-based defect segmentation and severity estimation of the defects in one two-branch network. Additionally, we show how incorporation of the production process parameters improves the model’s performance. After manually constructing a real-life industrial dataset, we first implemented and trained two single-task models performing the defect segmentation and severity estimation tasks separately. Next, we compared this to a multi-task model that simultaneously performs the two tasks at hand. By combining the tasks into one model, both segmentation tasks improved by 2.5% and 3% mIoU, respectively. In the next step, we extended the multi-task model using sensor fusion with process parameters. We demonstrate that the incorporation of the process parameters resulted in a further mIoU increase of 6.8% and 2.9% for the defect segmentation and severity estimation tasks, respectively.


Author(s):  
Jatin Arora ◽  
Claudio Maia ◽  
Syed Aftab Rashid ◽  
Geoffrey Nelissen ◽  
Eduardo Tovar

2020 ◽  
Vol 22 (Supplement_2) ◽  
pp. ii84-ii84
Author(s):  
Edgar Cabrera ◽  
Nelson Aponte ◽  
Johnny Garcia ◽  
Fredy Salazar ◽  
Eric Bouffet ◽  
...  

Abstract INTRODUCTION Primary central nervous system (CNS) sarcomas are rare mesenchymal non-meningothelial tumors accounting for less than 0.2% of intracranial lesions. Diagnosis and management are challenging due to the current lack of substantive clinical, histological and molecular data. METHODS We retrospectively identified all patients with diagnosis of primary CNS sarcoma at the Hospital Fundación Pediatrico la Misericordia (HOMI) in Bogota, Colombia. We collected patient demographics, disease characteristics, and outcomes for analysis. RESULTS Between 2008 and 2020, twenty-four consecutive patients were diagnosed at the HOMI representing 6% of all CNS tumors diagnosed over the same time period. The median age at presentation was 9.48 years (range:1.6–13.4). The median time of symptoms prior to diagnosis was 2 weeks (0.1–24). The most common presentation was headache (21/24- 89%) and vomiting (19/24- 79%). The frontal lobe was involved in 63% of patients (15/24) and only one patient presented with a cerebellar lesion. Histologically, these tumors were characterized by a pleomorphic spindle cell architecture and high mitotic activity. All samples lacked immunoreactivity to GFAP, CD34, EMA, and S100 and all samples had strong nuclear immunopositivity for TLE-1; BCL-2 was reactive in eighteen cases. Gross total resection was attained in fifteen patients, most patients received focal radiation therapy and ICE chemotherapy. Progression-free survival at 12 and 24 months was 57% and 31% respectively. Overall survival was 77% at 12 months and 39% at 24 months. Thirteen patients relapsed, 11 presented with local failures, and 2 with intracranial recurrences outside of the radiation field. CONCLUSION Our study identifies TLE-1 as a diagnostic marker of primary CNS sarcoma, a highly malignant supratentorial tumor of childhood. Further molecular studies are urgently needed to elucidate the biology of this disease and the unusually high incidence observed in the Colombian pediatric population.


Nano Letters ◽  
2021 ◽  
Author(s):  
Aya Nassereddine ◽  
Ahmed Abdelrahman ◽  
Emmanuelle Benard ◽  
Frederic Bedu ◽  
Igor Ozerov ◽  
...  

Cells ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 2089 ◽  
Author(s):  
Iker Lamas ◽  
Nathalie Weber ◽  
Sophie G. Martin

The small GTPase Cdc42 is critical for cell polarization in eukaryotic cells. In rod-shaped fission yeast Schizosaccharomyces pombe cells, active GTP-bound Cdc42 promotes polarized growth at cell poles, while inactive Cdc42-GDP localizes ubiquitously also along cell sides. Zones of Cdc42 activity are maintained by positive feedback amplification involving the formation of a complex between Cdc42-GTP, the scaffold Scd2, and the guanine nucleotide exchange factor (GEF) Scd1, which promotes the activation of more Cdc42. Here, we use the CRY2-CIB1 optogenetic system to recruit and cluster a cytosolic Cdc42 variant at the plasma membrane and show that this leads to its moderate activation also on cell sides. Surprisingly, Scd2, which binds Cdc42-GTP, is still recruited to CRY2-Cdc42 clusters at cell sides in individual deletion of the GEFs Scd1 or Gef1. We show that activated Cdc42 clusters at cell sides are able to recruit Scd1, dependent on the scaffold Scd2. However, Cdc42 activity is not amplified by positive feedback and does not lead to morphogenetic changes, due to antagonistic activity of the GTPase activating protein Rga4. Thus, the cell architecture is robust to moderate activation of Cdc42 at cell sides.


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