Academic literature on the topic 'Expressed sequence tags (EST)'

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Journal articles on the topic "Expressed sequence tags (EST)"

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Györgyey, János, Danièle Vaubert, José I. Jiménez-Zurdo, et al. "Analysis of Medicago truncatula Nodule Expressed Sequence Tags." Molecular Plant-Microbe Interactions® 13, no. 1 (2000): 62–71. http://dx.doi.org/10.1094/mpmi.2000.13.1.62.

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Systematic sequencing of expressed sequence tags (ESTs) can give a global picture of the assembly of genes involved in the development and function of organs. Indeterminate nodules representing different stages of the developmental program are especially suited to the study of organogenesis. With the vector λHybriZAP, a cDNA library was constructed from emerging nodules of Medicago truncatula induced by Sinorhizobium meliloti. The 5′ ends of 389 cDNA clones were sequenced, then these ESTs were analyzed both by sequence homology search and by studying their expression in roots and nodules. Two
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Cutri, Lucas, and Marcelo Carnier Dornelas. "PASSIOMA: Exploring Expressed Sequence Tags during Flower Development inPassifloraspp." Comparative and Functional Genomics 2012 (2012): 1–11. http://dx.doi.org/10.1155/2012/510549.

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The genusPassifloraprovides a remarkable example of floral complexity and diversity. The extreme variation ofPassifloraflower morphologies allowed a wide range of interactions with pollinators to evolve. We used the analysis of expressed sequence tags (ESTs) as an approach for the characterization of genes expressed duringPassiflorareproductive development. Analyzing thePassiflorafloral EST database (named PASSIOMA), we found sequences showing significant sequence similarity to genes known to be involved in reproductive development such as MADS-box genes. Some of these sequences were studied u
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Ozdemir Ozgenturk, Nehir, Fatma Oruç, Ugur Sezerman, et al. "Generation and Analysis of Expressed Sequence Tags fromOlea europaeaL." Comparative and Functional Genomics 2010 (2010): 1–9. http://dx.doi.org/10.1155/2010/757512.

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Olive (Olea europaeaL.) is an important source of edible oil which was originated in Near-East region. In this study, two cDNA libraries were constructed from young olive leaves and immature olive fruits for generation of ESTs to discover the novel genes and search the function of unknown genes of olive. The randomly selected 3840 colonies were sequenced for EST collection from both libraries. Readable 2228 sequences for olive leaf and 1506 sequences for olive fruit were assembled into 205 and 69 contigs, respectively, whereas 2478 were singletons. Putative functions of all 2752 differentially
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Watanabe, Hajime, Norihisa Tatarazako, Shigeto Oda, et al. "Analysis of expressed sequence tags of the water flea Daphnia magna." Genome 48, no. 4 (2005): 606–9. http://dx.doi.org/10.1139/g05-038.

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To study gene expression in the water flea Daphnia magna we constructed a cDNA library and characterized the expressed sequence tags (ESTs) of 7210 clones. The EST sequences clustered into 2958 nonredundant groups. BLAST analyses of both protein and DNA databases showed that 1218 (41%) of the unique sequences shared significant similarities to known nucleotide or amino acid sequences, whereas the remaining 1740 (59%) showed no significant similarities to other genes. Clustering analysis revealed particularly high expression of genes related to ATP synthesis, structural proteins, and proteases.
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Bettini, Ezio, Angela R. Porta, Norbert Dahmen, Henry Wang, and Frank L. Margolis. "Expressed sequence tags (EST) identify genes preferentially expressed in catfish chemosensory tissues." Molecular Brain Research 23, no. 4 (1994): 285–91. http://dx.doi.org/10.1016/0169-328x(94)90237-2.

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Levi, Amnon, Angela Davis, Pat Wechter, Alvaro Hernandez, and Jyothi Thimmapuram. "DEVELOPING EXPRESSED SEQUENCED TAGS (ESTS) FOR WATERMELON FRUIT." HortScience 41, no. 3 (2006): 518F—519. http://dx.doi.org/10.21273/hortsci.41.3.518f.

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A cDNA library was assembled using mRNA of watermelon fruit. The cDNA library was normalized and subtracted by hybridization with leaf cDNA of the same watermelon cultivar (Illini Red). 1,046 cDNA clones were sequenced to identify genes associated with fruit development and quality. Of 1,046 cDNA clones sequenced, 832 were unique sequences and designated as expressed sequenced tags (ESTs). Of the 832 ESTs, 205 (24.6%) have not been reported in any other plant species. Additionally, 186 ESTs (22.4%) correspond to genes with unknown function, while 441 ESTs (53.0%) correspond to genes with known
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Dyhrman, Sonya T., Sheean T. Haley, Shanda R. Birkeland, Louie L. Wurch, Michael J. Cipriano, and Andrew G. McArthur. "Long Serial Analysis of Gene Expression for Gene Discovery and Transcriptome Profiling in the Widespread Marine Coccolithophore Emiliania huxleyi." Applied and Environmental Microbiology 72, no. 1 (2006): 252–60. http://dx.doi.org/10.1128/aem.72.1.252-260.2006.

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ABSTRACT The abundant and widespread coccolithophore Emiliania huxleyi plays an important role in mediating CO2 exchange between the ocean and the atmosphere through its impact on marine photosynthesis and calcification. Here, we use long serial analysis of gene expression (SAGE) to identify E. huxleyi genes responsive to nitrogen (N) or phosphorus (P) starvation. Long SAGE is an elegant approach for examining quantitative and comprehensive gene expression patterns without a priori knowledge of gene sequences via the detection of 21-bp nucleotide sequence tags. E. huxleyi appears to have a rob
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Das, Nabajit, Saswat Suvesh Rout, and Rajanikanta Mahapatra. "An In-silico attempt to catch hold of the novel microRNAs in the Bio Energy Plant (Jatropha curcus): A Big Search." Biomirror 3, no. 07 (2012): 21–24. https://doi.org/10.5281/zenodo.30713.

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The oil-rich and weedy plant Jatropha has been hailed as the most promising source of biofuel on the planet, as a non-food, droughtresistant and oil-rich crop, Jatropha curcas fulfils many of the requirements for biofuel industries. A better understanding of the biochemical pathway leading to the synthesis of Jatropha oil and its regulation both by exogenous and endogenous factors is essential for facilitating increased yield. Increasing evidence has shown that miRNAs play multiple roles in various biological processes. The research finds previously known miRNAs from various plant species expr
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Livingstone, J. M., P. Seguin, and M. V. Strömvik. "An in silico study of the genes for the isoflavonoid pathway enzymes in soybean reveals novel expressed homologues." Canadian Journal of Plant Science 90, no. 4 (2010): 453–69. http://dx.doi.org/10.4141/cjps08214.

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Soybean [Glycine max (L.) Merr.] is an important source of isoflavones used by the nutraceutical industry. The soybean genome (2n = 40, 975 Mb) has recently been sequenced, and over a million (redundant) gene tags (expressed sequence tags, ESTs) are available in public databases. Using bioinformatics, we investigated five key enzymes of the isoflavonoid pathway (i.e., chalcone isomerase, isoflavone synthase, 2-hydroxyisoflavanone dehydratase, isoflavanone-7-O-glycosyltransferase, and isoflavone-7-O-glucoside-6′′-O-malonyltransferase) to gain a better understanding of which gene homologues are
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Burki, Fabien, Sergey I. Nikolaev, Ignacio Bolivar, Jackie Guiard, and Jan Pawlowski. "Analysis of expressed sequence tags from a naked foraminiferan Reticulomyxa filosa." Genome 49, no. 8 (2006): 882–87. http://dx.doi.org/10.1139/g06-048.

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Foraminifers are a major component of modern marine ecosystems and one of the most important oceanic producers of calcium carbonate. They are a key phylogenetic group among amoeboid protists, but our knowledge of their genome is still mostly limited to a few conserved genes. Here, we report the first study of expressed genes by means of expressed sequence tag (EST) from the freshwater naked foraminiferan Reticulomyxa filosa. Cluster analysis of 1630 valid ESTs enabled the identification of 178 groups of related sequences and 871 singlets. Approximately 50% of the putative unique 1059 ESTs coul
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Dissertations / Theses on the topic "Expressed sequence tags (EST)"

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Zhang, Yuan. "MST Based Ab Initio Assembler of Expressed Sequence Tags." Miami University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=miami1273245641.

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Alexsson, Andrei. "Unsupervised hidden Markov model for automatic analysis of expressed sequence tags." Thesis, Linköpings universitet, Bioinformatik, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-69575.

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This thesis provides an in-depth analyze of expressed sequence tags (EST) that represent pieces of eukaryotic mRNA by using unsupervised hidden Markov model (HMM). ESTs are short nucleotide sequences that are used primarily for rapid identificationof new genes with potential coding regions (CDS). ESTs are made by sequencing on double-stranded cDNA and the synthesizedESTs are stored in digital form, usually in FASTA format. Since sequencing is often randomized and that parts of mRNA contain non-coding regions, some ESTs will not represent CDS.It is desired to remove these unwanted ESTs if the p
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Godwin, Michael Jason. "Molecular Mapping of Disease-Related Expressed Sequence Tags and Resistance Gene Analogues in Soybean." Thesis, Virginia Tech, 2003. http://hdl.handle.net/10919/35550.

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Soybean has become one of the most important crops to the United States, resulting in a need to improve its disease resistance. The objectives of this study were to 1) design primers and develop PCR-based markers from disease-related expressed sequence tags (ESTs) and resistance gene analogues (RGAs), 2) assess the utility of such markers by diversity analysis of 12 soybean parental lines, and 3) search for possible association of the markers with known disease resistance genes by constructing a linkage map. The diversity analysis will allow this study to determine how well each marker can d
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Alcalde, Felipe Santiago Chambergo. "Elucidação do destino metabólico de glicose no fungo filamentoso Trichoderma reesei por análise EST (Expressed Sequence Tags) e "microarrays" de cDNA." Universidade de São Paulo, 2002. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-11022003-130558/.

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Apesar do intenso interesse na regulação metabólica e evolução das vias produtoras de ATP, o porquê de a maioria dos microorganismos multicelulares metabolizarem glicose através de respiração, ao invés da fermentação, ainda permanece sem resposta. Um desses microorganismos é o fungo celulolítico Trichoderma reesei (Hypocrea jecorina. Usando análise EST e microarrays de cDNA, foi estabelecido, em T. reesei, que a expressão dos genes que codificam as enzimas do ciclo de TCA é programada de tal modo a favorecer a oxidação de piruvato pelo ciclo de TCA, ao invés de sua redução a etanol, através
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Koo, Hyun Jo, Eric McDowell, Xiaoqiang Ma, et al. "Ginger and turmeric expressed sequence tags identify signature genes for rhizome identity and development and the biosynthesis of curcuminoids, gingerols and terpenoids." BioMed Central, 2013. http://hdl.handle.net/10150/610084.

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BACKGROUND:Ginger (Zingiber officinale) and turmeric (Curcuma longa) accumulate important pharmacologically active metabolites at high levels in their rhizomes. Despite their importance, relatively little is known regarding gene expression in the rhizomes of ginger and turmeric.RESULTS:In order to identify rhizome-enriched genes and genes encoding specialized metabolism enzymes and pathway regulators, we evaluated an assembled collection of expressed sequence tags (ESTs) from eight different ginger and turmeric tissues. Comparisons to publicly available sorghum rhizome ESTs revealed a total of
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Pollock, Stephanie. "A study of genetic diversity and genome organization of Brassica napus using EST (expressed sequence tags) of Arabidopsis and SSR (simple sequence repeat) markers of B. napus /." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33023.

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Arabidopsis expressed sequence tags (ESTs) and microsatellites of Brassica napus have been developed and used as PCR-based markers for both mapping and genetic diversity studies in B. napus . Out of 300 random Arabidopsis ESTs screened, 43 markers were mapped onto a genetic map of B. napus and then used in a diversity study involving 48 B. napus cultivars. A second set of EST markers were developed from chromosome 1 of Arabidopsis and used in genetic mapping studies of B. napus. From 192 primer pairs developed, 50 markers were added onto the B. napus reference map. Microsatellite markers were
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Esteves, Michelle Pereira. "Systematic analysis of expressed sequence tag (EST) databases to identify novel breast markers in breast cancer." Thesis, Royal Holloway, University of London, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.537516.

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Silva, Marcicleide Lima da. "Estudo de genes expressos em frutos de camu-camu: seqüenciamento de ests." Universidade Federal do Amazonas, 2006. http://tede.ufam.edu.br/handle/tede/4385.

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Submitted by Alisson Mota (alisson.davidbeckam@gmail.com) on 2015-07-13T19:18:49Z No. of bitstreams: 1 Tese - Marcicleide Lima do Espirito Santo.pdf: 7339955 bytes, checksum: 22519cc9c5e5f14e2991f1e20ddb938f (MD5)<br>Approved for entry into archive by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2015-07-15T18:14:34Z (GMT) No. of bitstreams: 1 Tese - Marcicleide Lima do Espirito Santo.pdf: 7339955 bytes, checksum: 22519cc9c5e5f14e2991f1e20ddb938f (MD5)<br>Approved for entry into archive by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2015-07-15T18:1
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Waikel, Patricia A. "Analysis of a Partial Expressed Sequence Tag (EST) Library and Differential Expression of Genes in Biochemical Morphotypes of the Marine Sponge Discodermia dissoluta." NSUWorks, 2010. http://nsuworks.nova.edu/occ_stuetd/197.

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A variety of secondary metabolites with promising antimicrobial and anti-tumor properties have been identified in marine organisms. Sponges, in particular, have been the source of several of these, including discodermolide from Discodermia dissoluta. While metagenomic studies have been undertaken to identify genes involved in discodermolide production, presently, a transcriptomic approach has not been taken to characterize the metagenome of D. dissoluta. Samples of D. dissoluta were collected from a site in the Bahamas and screened for secondary metabolite production. Some specimens of D. diss
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Alves, Helena Javiel. "Identificação e caracterização de seqüências expressas (EST) na musculatura peitoral de frangos de corte." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/11/11139/tde-11012005-161916/.

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A produção de aves no Brasil vem crescendo na ordem de 10% a cada ano, o que se explica pela atualização constante da tecnologia do setor (http://www.abef.com.br). Sendo a carne de frango a fonte de proteína animal mais barata e acessível ao consumidor, há necessidade de se produzir cada vez mais animais com maior acúmulo de massa muscular. Para isso, o entendimento dos mecanismos celulares e moleculares envolvidos na formação da musculatura esquelética é de extrema relevância. Os fatores miogênicos, genes responsáveis pela determinação e diferenciação de células musculares, foram clonados e p
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Books on the topic "Expressed sequence tags (EST)"

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Parkinson, John, ed. Expressed Sequence Tags (ESTs). Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-136-3.

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Rune, Matthiesen, ed. Mass spectrometry data analysis in proteomics. Humana Press, 2007.

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Matthiesen, Rune. Mass spectrometry data analysis in proteomics. Humana Press, 2013.

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Expressed Sequence Tags (ESTs). Humana Press, 2008.

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Parkinson, John. Expressed Sequence Tags: Generation and Analysis. Humana Press, 2010.

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Expressed Sequence Tags: Generation and Analysis. Humana Press, 2009.

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Matthiesen, Rune. Mass Spectrometry Data Analysis in Proteomics. Springer New York, 2019.

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Matthiesen, Rune. Mass Spectrometry Data Analysis in Proteomics. Humana Press, 2010.

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Matthiesen, Rune. Mass Spectrometry Data Analysis in Proteomics. Springer New York, 2020.

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Matthiesen, Rune. Mass Spectrometry Data Analysis in Proteomics. Humana Press, 2016.

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Book chapters on the topic "Expressed sequence tags (EST)"

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Al-Faifi, Sulieman A., Hussein M. Migdadi, Salem S. Algamdi, et al. "Analysis of Expressed Sequence Tags (EST) in Date Palm." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7159-6_23.

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Pedretti, Kevin, Todd Scheetz, Terry Braun, Chad Roberts, Natalie Robinson, and Thomas Casavant. "A Parallel Expressed Sequence Tag (EST) Clustering Program." In Lecture Notes in Computer Science. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44743-1_51.

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Clifton, Sandra W., and Makedonka Mitreva. "Strategies for Undertaking Expressed Sequence Tag (EST) Projects." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-136-3_2.

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Schmitt, Armin O. "Mining Expressed Sequence Tag (EST) Libraries for Cancer-Associated Genes." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-545-9_6.

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Joshi, Aruna G., and Ashutosh R. Pathak. "EST (Expressed Sequence Tag): A Technique for Identification of Plant Secondary Metabolite Genes." In Plant and Human Health, Volume 2. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-03344-6_8.

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Wolfsberg, Tyra G., and David Landsman. "Expressed Sequence Tags (ESTs)." In Methods of Biochemical Analysis. John Wiley & Sons, Inc., 2002. http://dx.doi.org/10.1002/0471223921.ch12.

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Parkinson, John, and Mark Blaxter. "Expressed Sequence Tags: An Overview." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-136-3_1.

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Susko, Edward, and Andrew J. Roger. "Statistical Analysis of Expressed Sequence Tags." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-136-3_13.

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Cheung, Foo. "Global Assembly of Expressed Sequence Tags." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-839-9_15.

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Wasmuth, James, and Mark Blaxter. "Obtaining Accurate Translations from Expressed Sequence Tags." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-136-3_10.

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Conference papers on the topic "Expressed sequence tags (EST)"

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Keng-Hoong Ng, Somnuk Phon-Amnuaisuk, and Chin-Kuan Ho. "Clustering of Expressed Sequence Tag (EST) with Markov models and self-organizing maps: An exploratory study." In 2008 International Symposium on Information Technology. IEEE, 2008. http://dx.doi.org/10.1109/itsim.2008.4631585.

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Reena, N., A. Chandrasekar, A. Riju, P. L. Nima, S. J. Eapen, and M. Anandaraj. "Gene identification inPhytophthora capsicithrough expressed sequence tags." In the International Symposium. ACM Press, 2010. http://dx.doi.org/10.1145/1722024.1722043.

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Adams, Mark D., Anthony R. Kerlavage, Mark Dubnick, Ruben F. Moreno, Chris Fields, and J. Craig Venter. "ANALYSIS OF EXPRESSED SEQUENCE TAGS FROM HUMAN BRAIN CDNAS." In Proceedings of the 2nd International Conference. WORLD SCIENTIFIC, 1993. http://dx.doi.org/10.1142/9789814503655_0010.

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Min, Xiangjia J., Gregory Butler, Reginald Storms, and Adrian Tsang. "Comparative Assessment of DNA Assemblers for Assembling Expressed Sequence Tags." In 2009 Ohio Collaborative Conference on Bioinformatics (OCCBIO). IEEE, 2009. http://dx.doi.org/10.1109/occbio.2009.19.

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Sim-Hui Tee. "Identification of the overexpressed genes in hepatocellular carcinoma using Expressed Sequence Tags." In 2012 International Conference on Biomedical Engineering (ICoBE). IEEE, 2012. http://dx.doi.org/10.1109/icobe.2012.6179078.

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Lee, Guo-Hsing, Nai-Yu Chuang, Wen-Dar Lin, Chung-Der Hsiao, Hahn-Ming Lee, and Jan-Ming Ho. "E2D: A Novel Tool for Annotating Protein Domains in Expressed Sequence Tags." In 2006 IEEE Symposium on Computational Intelligence and Bioinformatics and Computational Biology. IEEE, 2006. http://dx.doi.org/10.1109/cibcb.2006.330967.

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Jain, M., H. Holz, J. Shrager, O. Vallon, C. Hauser, and A. Grossman. "A Hybrid, Recursive Algorithm for Clustering Expressed Sequence Tags in Chlamydomonas reinhardtii." In 18th International Conference on Pattern Recognition (ICPR'06). IEEE, 2006. http://dx.doi.org/10.1109/icpr.2006.87.

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Gong, Ping, Fuliang Xie, Baohong Zhang, and Edward J. Perkins. "In silico identification of microRNAs from expressed sequence tags of three earthworm species." In the First ACM International Conference. ACM Press, 2010. http://dx.doi.org/10.1145/1854776.1854847.

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Wati, Ridha, Mohammad Basyuni, Shigeyuki Baba, and Hirosuke Oku. "Bioinformatics analysis of the expressed sequence tags from Rhizophora stylosa Griff. genomic library." In INVENTING PROSPEROUS FUTURE THROUGH BIOLOGICAL RESEARCH AND TROPICAL BIODIVERSITY MANAGEMENT: Proceedings of the 5th International Conference on Biological Science. Author(s), 2018. http://dx.doi.org/10.1063/1.5050147.

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Ng, Keng-Hoong, Somnuk Phon-Amnuaisuk, and Chin-Kuan Ho. "Clustering of expressed sequence tags with distance measure based on Burrows-Wheeler transform." In 2010 3rd International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2010. http://dx.doi.org/10.1109/bmei.2010.5639798.

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Reports on the topic "Expressed sequence tags (EST)"

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อิ่มจงใจรัก, จันทร์ประภา. การแยกและการศึกษาลักษณะสมบัติของเปปไทด์ต้านจุลชีพจากเซลล์เม็ดเลือดของปูทะเล Scylla paramamosain : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2009. https://doi.org/10.58837/chula.res.2009.52.

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เปปไทด์ต้านจุลชีพเป็นเปปไทด์สายสั้นที่มีความสำคัญต่อระบบภูมิคุ้มกันของร่างกายของสิ่งมีชีวิตหลายชนิดโดยมีคุณสมบัติที่สามารถต่อต้านการติดเชื้อที่เกิดจากจุลชีพได้ ในงานวิจัยนี้ได้ทำการค้นหาลำดับนิวคลีโอไทด์ที่สมบูรณ์(full length cDNA) ของยีนเปปไทด์ต้านจุลชีพครัสติน(CrusSp)ศึกษาลักษณะสมบัติของยีนรวมทั้งแยกและวิเคราะห์การจัดเรียงตัวของยีน(genomicorganization)จากการค้นหาลำดับนิวคลีโอไทด์ที่สมบูรณ์ของยีนเปปไทด์ต้านจุลชีพครัสตินจากเซลล์เม็ดเลือดแดงของปูทะเล(Scylla paramamosain) โดยเทคนิค expressed sequence tag(EST) และ rapid amplification cDNA end (RACE) พบว่าประกอบด้วย ORF ขนาด 336 bp ที่สามารถถอดรหั
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นุชประยูร, อิศรางค์, มณฑน์มาศ สุนทราวัฒน์ та ธัญณิชา อ่อนดี. การศึกษาโปรตีน ที่สำคัญในพิษงูแมวเซาเพื่อนำมาดัดแปลงใช้ประโยชน์ทางการแพทย์ : รายงานการวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์มหาวิทยาลัย, 2009. https://doi.org/10.58837/chula.res.2009.23.

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Abstract:
ปัญหางูพิษกัดเป็นปัญหาทางสาธารณะสุขที่สำคัญของประเทศไทย หนึ่งในงูพิษที่สำคัญในไทยคืองูแมวเซา (Daboia russellii siamensis) งูชนิดนี้พบมากในแถบภาคกลางและภาคตะวันออกของไทย ผู้ที่ถูกงูชนิดนี้กัด มักมีอาการทางระบบเลือด และภาวะไตวายเฉียบพลัน ซึ่งเป็นสาเหตุสำคัญที่ทำให้ผู้ที่ถูกงูแมวเซากัดเสียชีวิต ในปัจจุบันความรู้เกี่ยวกับกลไกการเกิดพิษหลังถูกงูแมวเซากัด รวมทั้งโปรตีนสำคัญในพิษงูแมวเซาที่อาจมีประโยชน์ทางการแพทย์ ยังไม่มีการศึกษาอย่างแน่ชัด การศึกษาองค์ประกอบของพิษงูแมวเซาในเชิงลึก จะช่วยให้เข้าใจกลไกการเกิดพิษ นำไปสู่การรักษาที่มีประสิทธิภาพที่ดีขึ้น พร้อมทั้งอาจนำความรู้ที่ได้ไปใช้ประโยชน์ในทางการ
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นุชประยูร, อิศรางค์. การศึกษาโปรตีนที่สำคัญในพิษงูแมวเซาเพื่อนำมาดัดแปลงใช้ประโยชน์ทางการแพทย์ : รายงานการวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์มหาวิทยาลัย, 2008. https://doi.org/10.58837/chula.res.2008.26.

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Abstract:
ปัญหางูพิษกัดเป็นปัญหาทางสาธารณสุขที่สำคัญของประเทศไทย หนึ่งในงูพิษที่สำคัญในไทยคือ งูแมวเซา (Daboia russellii siamensis) งูชนิดนี้พบมากในแถบภาคกลางและภาคตะวันออกของไทย ผู้ที่ถูกงูชนิดนี้กัด มักมีอาการทางระบบเลือด และภาวะไตวายเฉียบพลัน ซึ่งเป็นสาเหตุสำคัญที่ทำให้ผู้ที่ถูกงูแมวเซากัดเสียชีวิต ในปัจจุบันความรู้เกี่ยวกับกลไกการเกิดพิษหลังถูกงูแมวเซากัด รวมทั้งโปรตีนสำคัญในพิษงูแมวเซาที่อาจมีประโยชน์ทางการแพทย์ ยังไม่มีการศึกษาอย่างแน่ชัด การศึกษาองค์ประกอบของพิษงูแมวเซาในเชิงลึก จะช่วยให้เข้าใจกลไกการเกิดพิษ นำไปสู่การรักษาที่มีประสิทธิภาพที่ดีขึ้น พร้อมทั้งอาจนำความรู้ที่ได้ไปใช้ประโยชน์ในทางการ
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