| 1. |
- Björk, Magnus, 1977, et al.
(författare)
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Exposed Datapath for Efficient Computing
- 2006
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- We introduce FlexCore, which is the first exemplar of a processor based on the FlexSoC processor paradigm. TheFlexCore utilizes an exposed datapath for increased performance. Microbenchmarks yield a performance boost of a factor of two over a traditional five-stage pipeline with the same functional units as the FlexCore.We describe our approach to compiling for the FlexCore.A flexible interconnect allows the FlexCore datapath to bedynamically reconfigured as a consequence of code generation. Additionally, specialized functional units may be introduced and utilized within the same architecture and compilation framework. The exposed datapath requires a wide control word. The conducted evaluation of two micro benchmarks confirms that this increases the instruction bandwidth and memory footprint. This calls for an efficient instruction decoding as proposed in the FlexSoC paradigm.
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| 4. |
- Thuresson, Martin, 1977, et al.
(författare)
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FlexCore: Utilizing Exposed Datapath Control for Efficient Computing
- 2009
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Ingår i: Journal of Signal Processing Systems. - : Springer Science and Business Media LLC. - 1939-8018 .- 1939-8115. ; 57:1, s. 5-19
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Tidskriftsartikel (refereegranskat)abstract
- We introduce FlexCore, the first exemplar of an architecture based on the FlexSoC framework. Comprising the same datapath units found in a conventional five-stage pipeline, the FlexCore has an exposed datapath control and a flexible interconnect to allow the datapath to be dynamically reconfigured as a consequence of code generation. Additionally, the FlexCore allows specialized datapath units to be inserted and utilized within the same architecture and compilation framework.This study shows that, in comparison to a conventional five-stage general-purpose processor, the FlexCore is up to 40\% more efficient in terms of cycle count on a set of benchmarks from the embedded application domain. We show that both the fine-grained control and the flexible interconnect contribute to the speedup. Furthermore, our synthesized, placed and routed FlexCore offers savings both in energy and execution time.The exposed FlexCore datapath requires a wide control word. The conducted evaluation confirms that this increases the instruction bandwidth and memory footprint. This calls for efficient instruction decoding as proposed in the FlexSoC framework.
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| 6. |
- Själander, Magnus, 1977, et al.
(författare)
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A Flexible Datapath Interconnect for Embedded Applications
- 2007
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Ingår i: IEEE Computer Society Annual Symposium on VLSI. ; , s. 15-20
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Konferensbidrag (refereegranskat)abstract
- We investigate the effects of introducing a flexible interconnect into an exposed datapath. We define an exposed datapath as a traditional GPP datapath that has its normal control removed, leading to the exposure of a wide control word. For an FFT benchmark, the introduction of a flexible interconnect reduces the total execution time by 16%. Compared to a traditional GPP, the execution time for an exposed datapath using a flexible interconnect is 32% shorter whereas the energy dissipation is 29% lower. Our investigation is based on a cycleaccurate architectural simulator and figures on delay, power, and area are obtained from placed-and-routed layouts in a commercial 0.13-ìm technology. The results from our case studies indicate that by utilizing a flexible interconnect, significant performance gains can be achieved for generic applications.
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| 7. |
- Engström, Gunnar, et al.
(författare)
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Pulmonary function and atherosclerosis in the general population : causal associations and clinical implications
- 2024
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Ingår i: European Journal of Epidemiology. - : Springer Nature. - 0393-2990 .- 1573-7284. ; 39:1, s. 35-49
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Tidskriftsartikel (refereegranskat)abstract
- Reduced lung function is associated with cardiovascular mortality, but the relationships with atherosclerosis are unclear. The population-based Swedish CArdioPulmonary BioImage study measured lung function, emphysema, coronary CT angiography, coronary calcium, carotid plaques and ankle-brachial index in 29,593 men and women aged 50–64 years. The results were confirmed using 2-sample Mendelian randomization. Lower lung function and emphysema were associated with more atherosclerosis, but these relationships were attenuated after adjustment for cardiovascular risk factors. Lung function was not associated with coronary atherosclerosis in 14,524 never-smokers. No potentially causal effect of lung function on atherosclerosis, or vice versa, was found in the 2-sample Mendelian randomization analysis. Here we show that reduced lung function and atherosclerosis are correlated in the population, but probably not causally related. Assessing lung function in addition to conventional cardiovascular risk factors to gauge risk of subclinical atherosclerosis is probably not meaningful, but low lung function found by chance should alert for atherosclerosis.
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| 8. |
- Haider, Zahra, et al.
(författare)
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An integrated transcriptome analysis in T-cell acute lymphoblastic leukemia links DNA methylation subgroups to dysregulated TAL1 and ANTP homeobox gene expression
- 2019
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Ingår i: Cancer Medicine. - : John Wiley & Sons. - 2045-7634. ; 8:1, s. 311-324
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Tidskriftsartikel (refereegranskat)abstract
- Classification of pediatric T‐cell acute lymphoblastic leukemia (T‐ALL) patients into CIMP (CpG Island Methylator Phenotype) subgroups has the potential to improve current risk stratification. To investigate the biology behind these CIMP subgroups, diagnostic samples from Nordic pediatric T‐ALL patients were characterized by genome‐wide methylation arrays, followed by targeted exome sequencing, telomere length measurement, and RNA sequencing. The CIMP subgroups did not correlate significantly with variations in epigenetic regulators. However, the CIMP+ subgroup, associated with better prognosis, showed indicators of longer replicative history, including shorter telomere length (P = 0.015) and older epigenetic (P < 0.001) and mitotic age (P < 0.001). Moreover, the CIMP+ subgroup had significantly higher expression of ANTP homeobox oncogenes, namely TLX3, HOXA9, HOXA10, and NKX2‐1, and novel genes in T‐ALL biology including PLCB4, PLXND1, and MYO18B. The CIMP− subgroup, with worse prognosis, was associated with higher expression of TAL1 along with frequent STIL‐TAL1 fusions (2/40 in CIMP+ vs 11/24 in CIMP−), as well as stronger expression of BEX1. Altogether, our findings suggest different routes for leukemogenic transformation in the T‐ALL CIMP subgroups, indicated by different replicative histories and distinct methylomic and transcriptomic profiles. These novel findings can lead to new therapeutic strategies.
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| 9. |
- Norberg, Anna, et al.
(författare)
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Novel variants in Nordic patients referred for genetic testing of telomere-related disorders
- 2018
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Ingår i: European Journal of Human Genetics. - : Nature Publishing Group. - 1018-4813 .- 1476-5438. ; 26:6, s. 858-867
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Tidskriftsartikel (refereegranskat)abstract
- Telomere-related disorders are a clinically and genetically heterogeneous group of disorders characterized by premature telomere shortening and proliferative failure of a variety of tissues. This study reports the spectrum of telomere-related gene variants and telomere length in Nordic patients referred for genetic testing due to suspected telomere-related disorder. We performed Sanger sequencing of the genes TERT, TERC, DKC1, and TINF2 on 135 unrelated index patients and measured telomere length by qPCR on DNA from peripheral blood leukocytes. We identified pathogenic or likely pathogenic variants in 10 index patients, all of which had short telomeres compared to age-matched healthy controls. Six of the 10 variants were novel; three in TERC (n.69_74dupAGGCGC, n.122_125delGCGG, and n.407_408delinsAA) and three in TERT (p.(D684G), p.(R774*), and p.(*1133Wext*39)). The high proportion of novel variants identified in our study highlights the need for solid interpretation of new variants that may be detected. Measurement of telomere length is a useful approach for evaluating pathogenicity of genetic variants associated with telomere-related disorders.
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