897 resultados para Sisu (automerkki)
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Analisa aspectos que influenciam a evasão discente nas graduações de instituições federais de ensino superior (Ifes) brasileiras – mas sem excluir menções pontuais a outras instituições de ensino superior (IES) públicas, quando julgado pertinente –, compreendendo essa temática no âmbito da expansão da rede federal de ensino superior no País e da adoção de programas como o Reuni e a implementação do Sistema de Seleção Unificada (SiSU).
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The human genome encodes the blueprint of life, but the function of the vast majority of its nearly three billion bases is unknown. The Encyclopedia of DNA Elements (ENCODE) project has systematically mapped regions of transcription, transcription factor association, chromatin structure and histone modification. These data enabled us to assign biochemical functions for 80% of the genome, in particular outside of the well-studied protein-coding regions. Many discovered candidate regulatory elements are physically associated with one another and with expressed genes, providing new insights into the mechanisms of gene regulation. The newly identified elements also show a statistical correspondence to sequence variants linked to human disease, and can thereby guide interpretation of this variation. Overall, the project provides new insights into the organization and regulation of our genes and genome, and is an expansive resource of functional annotations for biomedical research.
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BACKGROUND: Pseudogenes have long been considered as nonfunctional genomic sequences. However, recent evidence suggests that many of them might have some form of biological activity, and the possibility of functionality has increased interest in their accurate annotation and integration with functional genomics data. RESULTS: As part of the GENCODE annotation of the human genome, we present the first genome-wide pseudogene assignment for protein-coding genes, based on both large-scale manual annotation and in silico pipelines. A key aspect of this coupled approach is that it allows us to identify pseudogenes in an unbiased fashion as well as untangle complex events through manual evaluation. We integrate the pseudogene annotations with the extensive ENCODE functional genomics information. In particular, we determine the expression level, transcription-factor and RNA polymerase II binding, and chromatin marks associated with each pseudogene. Based on their distribution, we develop simple statistical models for each type of activity, which we validate with large-scale RT-PCR-Seq experiments. Finally, we compare our pseudogenes with conservation and variation data from primate alignments and the 1000 Genomes project, producing lists of pseudogenes potentially under selection. CONCLUSIONS: At one extreme, some pseudogenes possess conventional characteristics of functionality; these may represent genes that have recently died. On the other hand, we find interesting patterns of partial activity, which may suggest that dead genes are being resurrected as functioning non-coding RNAs. The activity data of each pseudogene are stored in an associated resource, psiDR, which will be useful for the initial identification of potentially functional pseudogenes.
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The transcriptome is the readout of the genome. Identifying common features in it across distant species can reveal fundamental principles. To this end, the ENCODE and modENCODE consortia have generated large amounts of matched RNA-sequencing data for human, worm and fly. Uniform processing and comprehensive annotation of these data allow comparison across metazoan phyla, extending beyond earlier within-phylum transcriptome comparisons and revealing ancient, conserved features. Specifically, we discover co-expression modules shared across animals, many of which are enriched in developmental genes. Moreover, we use expression patterns to align the stages in worm and fly development and find a novel pairing between worm embryo and fly pupae, in addition to the embryo-to-embryo and larvae-to-larvae pairings. Furthermore, we find that the extent of non-canonical, non-coding transcription is similar in each organism, per base pair. Finally, we find in all three organisms that the gene-expression levels, both coding and non-coding, can be quantitatively predicted from chromatin features at the promoter using a 'universal model' based on a single set of organism-independent parameters.
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Diplomityön tavoitteena oli löytää uusi kaarevahampaisten kartiopyörien toimittaja tulevaisuuden tuoteperheelle Sisu Akselit Oy:ssä. Kirjallisuustutkimuksen osuudessa perehdyttiin toimittajanvalintaprosessin eri osa-alueisiin. Käsiteltäviä alueita olivat mm. markkinatekijät, toimittajasuhteen ominaisuudet ja valintaprosessin työvaiheet sekä muutamat prosessin työkalut. Soveltavan osan alussa muodostettiin malli valintaprosessin läpiviemiseksi. Malli koostuu viidestä vaiheesta, joista ensimmäiset neljä toteutettiin diplomityön puitteista. Ensimmäinen vaihe sisältää yrityksen sisäisen analyysin, toinen toimittajamarkkinoiden tutkimuksen yrityksen ulkopuolella, kolmas hankinnan strategiavaihtoehtojen määrittämisen ja neljäs valintojen tekemisen. Viidennessä vaiheessa sovitaan toimituksen yksityiskohdista ja aloitetaan toimitukset. Työn tuloksena saatiin määritettyä toimittajasuhdestrategia Sisu Akselit Oy:n kaarevahampaisten kartiopyörien hankinnalle uudella tuoteperheellä. Valittuun suhdestrategiaan rajattiin suuresta joukosta kolme parhaiten sopivaa potentiaalista toimittajaa. Markkinoilla olevien valmistajien toiminnan tehokkuudessa havaittiin suuria eroja. Näin valintojen tuloksena arvioidaan saavutettavan kustannussäästöjä nykytilaan verrattuna. Työn sivutuotteena syntyi strategisen komponentin toimittajavalintamalli, jota voitaneen yrityksessä soveltaa jatkossakin.
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kuv., 15 x 22 cm
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14 x 22 cm
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14 x 22 cm
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14 x 22 cm
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17 x 24 cm
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22 x 27 cm
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kuv., 14 x 20 cm
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kuv., 10 x 19 cm