Relevant bibliographies by topics / SNaPshot assay

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'SNaPshot assay'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "SNaPshot assay"

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Lamy, A., E. Labourier, O. Prigneau, F. Di Fiore, R. Sesboüá, and J. Sabourin. "A method to assess KRAS/BRAF genotype in patients with metastatic colorectal cancer (mCRC) elligible for anti-EGFR therapies." Journal of Clinical Oncology 29, no. 4_suppl (2011): 383. http://dx.doi.org/10.1200/jco.2011.29.4_suppl.383.

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383 Background: KRAS/BRAF mutation screening is a new diagnostic tool since activating mutations, especially for KRAS, are strong negative predictive factors for anti-EGFR monoclonal antibody therapies. Therefore, standardized, reliable, and rapid mutation detection methods are needed. The goal of the present study is to evaluate the concordance between a clinically validated laboratory-developed KRAS/BRAF SNaPshot test and a novel research use assay, the Signature KRAS/BRAF Mutations kit (Asuragen Inc.), in representative clinical specimens. Methods: Genomic DNA from FFPE mCRC specimens previ
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Qu, K. Z., Y. Ren, J. Liu, A. Sferrozza, and R. A. Bender. "Detection of seven polymorphisms associated with colorectal cancer therapeutic response and toxicity." Journal of Clinical Oncology 24, no. 18_suppl (2006): 13160. http://dx.doi.org/10.1200/jco.2006.24.18_suppl.13160.

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13160 Background: First-line therapy for metastatic colorectal cancer (CRC) is 5-fluorouracil/leucovorin in combination with oxaliplatin (ie, FOLFOX™) or irinotecan (ie, FOLFIRI). Optimizing this therapy for an individual patient, however, is complicated due to wide variability in drug response and potential for toxicity. Such variability may be due to functional genomic polymorphisms in the drug target gene or in the metabolizing or DNA repair enzyme genes. We report, herein, development and validation of 2 new assays that, together, detect 7 polymorphisms associated with CRC drug response an
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Budowle, Sarah A., Suzanne Gonzalez, Bruce Budowle, Arthur J. Eisenberg, and Robert W. Grange. "A novel SNaPshot assay to detect themdx mutation." Muscle & Nerve 37, no. 6 (2008): 731–35. http://dx.doi.org/10.1002/mus.21027.

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Spaniolas, Stelios, Christos Bazakos, Gregory A. Tucker, and Malcolm J. Bennett. "Comparison of SNP-Based Detection Assays for Food Analysis: Coffee Authentication." Journal of AOAC INTERNATIONAL 97, no. 4 (2014): 1114–20. http://dx.doi.org/10.5740/jaoacint.13-237.

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Abstract Recently, DNA-based authentication methods were developed to serve as complementary approaches to analytical chemistry techniques. The single nucleotide polymorphism (SNP)-based reaction chemistries, when combined with the existing detection methods, could result in numerous analytical approaches, all with particular advantages and disadvantages. The dual aim of this study was (a) to develop SNP-based analytical assays such as the single-base primer extension (SNaPShotTM) and pyrosequencing in order to differentiate Arabica and Robusta varieties for the authentication of coffee beans
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Mukherjee, Sayak, David Stewart, William Stewart, Lewis L. Lanier, and Jayajit Das. "Connecting the dots across time: reconstruction of single-cell signalling trajectories using time-stamped data." Royal Society Open Science 4, no. 8 (2017): 170811. http://dx.doi.org/10.1098/rsos.170811.

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Single-cell responses are shaped by the geometry of signalling kinetic trajectories carved in a multidimensional space spanned by signalling protein abundances. It is, however, challenging to assay a large number (more than 3) of signalling species in live-cell imaging, which makes it difficult to probe single-cell signalling kinetic trajectories in large dimensions. Flow and mass cytometry techniques can measure a large number (4 to more than 40) of signalling species but are unable to track single cells. Thus, cytometry experiments provide detailed time-stamped snapshots of single-cell signa
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Vinayagamoorthy, Thuraiayah, David Zhang, Fei Ye, Dilanthi Vinayagamoorthy, and Roger Hodkinson. "Can detection of Braf p.V600E mutation be improved? Comparison of allele specific multiplex sequencing to present tests." Journal of Solid Tumors 7, no. 2 (2017): 14. http://dx.doi.org/10.5430/jst.v7n2p14.

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Objective: This is an investigative study to evaluate a new companion diagnostic platform, allele specific multiplex sequencing(ASMS). Detection of Braf p.V600E from solid tumors is used as the test model with the following objectives: 1) whether ASMScan detect Braf p.V600E/K mutations from a variety of solid tumors, 2) whether ASMS can detect all Braf p.V600E from samplesthat were positive for Braf V600E by SNaPshot or Ion Torrent, and 3) whether ASMS can detect Braf p.V600E among samplesthat were reported negative by SNaPshot or Ion Torrent.Methods: ASMS is a novel modification (US Patent 61
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Ghosh, Debarati, Sailesh Gochhait, Disha Banerjee, Anindita Chatterjee, Swagata Sinha, and Krishnadas Nandagopal. "SNaPshot Assay in Quantitative Detection of Allelic Nondisjunction in Down Syndrome." Genetic Testing and Molecular Biomarkers 16, no. 10 (2012): 1226–35. http://dx.doi.org/10.1089/gtmb.2012.0083.

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Huang, Chien-Hsun, Mu-Tzu Chang, Mu-Chiou Huang, and Fwu-Ling Lee. "Rapid identification of Lactobacillus plantarum group using the SNaPshot minisequencing assay." Systematic and Applied Microbiology 34, no. 8 (2011): 586–89. http://dx.doi.org/10.1016/j.syapm.2011.02.006.

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Smith, J. A., and H. Godfrey. "A SNaPshot™ assay for the identification of forensically important blowflies." Forensic Science International: Genetics Supplement Series 3, no. 1 (2011): e479-e480. http://dx.doi.org/10.1016/j.fsigss.2011.09.101.

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Lou, Chunguang, Bin Cong, Shujin Li, et al. "A SNaPshot assay for genotyping 44 individual identification single nucleotide polymorphisms." ELECTROPHORESIS 32, no. 3-4 (2010): 368–78. http://dx.doi.org/10.1002/elps.201000426.

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Dissertations / Theses on the topic "SNaPshot assay"

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Misyak, Sarah A. "Development of a SNP Assay for the Differentiation of Allelic Variations in the mdx Dystrophic Mouse Model." Thesis, Virginia Tech, 2008. http://hdl.handle.net/10919/32325.

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The purpose of this study was to develop a SNaPshot® assay to simultaneously discriminate between the dystrophic and wild type (wt) alleles in mdx mice. The mdx mouse is an animal model for Duchenne muscular dystrophy (DMD), a severe and fatal muscle wasting disease. To evaluate possible treatments and to carry out genetic studies, it is essential to distinguish between mice that carry the mutant dystrophic or wt allele(s). The current Amplification-Resistant Mutation System (ARMS) assay used to genotype mdx mice is labor intensive and sometimes fails to yield typing results, which reduce i
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Fröhlich, Yvonne [Verfasser], and Micaela [Akademischer Betreuer] Poetsch. "Entwicklung und Etablierung mehrerer Snapshot-Assays zur Bestimmung mitochondrialer Haplogruppen in unterschiedlichen europäischen und afrikanischen Populationen / Yvonne Fröhlich ; Betreuer: Micaela Poetsch." Duisburg, 2018. http://d-nb.info/1164376438/34.

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Witt, Lisa-Marie [Verfasser], and Micaela [Akademischer Betreuer] Poetsch. "Etablierung von SNaPshot-Assays zur Charakterisierung Y-chromosomaler Haplogruppen – ein Teilprojekt zur Bestimmung der Ursprungspopulation unbekannter Tatortspuren / Lisa-Marie Witt ; Betreuer: Micaela Poetsch." Duisburg, 2018. http://d-nb.info/1156533473/34.

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Shih, Hui-Lin, and 史蕙菱. "Detection of EGFR Gene Mutations by Combination of Amplified Fragment Length Difference and SNaPshot Assay." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/59733490794445693211.

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碩士<br>國防醫學院<br>病理及寄生蟲學研究所<br>101<br>The epidermal growth factor receptor (EGFR) belongs to the receptor tyrosine kinase (RTK) family. A mutant EGFR could remain constant phosphorylation which elicits downstream activation and signaling for cell proliferation and even tumor formation. Mutations of EGFR have been reported in several types of cancer, and they are the target of new anticancer therapies. These mutations have to be identified before prescribing the personalized anticancer therapy. Deletion of exon 19 (53.4%) and L858R point mutation (43.8%) are two most common mutant genotypes of EG
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Book chapters on the topic "SNaPshot assay"

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Hayes, David, and Geoff Mellor. "High throughput screening – considerations for enzyme assays." In Enzyme Assays. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780199638208.003.0011.

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Abstract The rapidly increasing number of potential therapeutic targets is leading the pharmaceutical industry to radically alter its drug discovery strategy (for reviews, see 1–6). For these targets, there is often little or no structural information available for the rational design of putative drug candidates. Additionally, there is a desire to obtain ‘lead’ molecules of novel structure, to avoid patent infringement of known inhibitors. One approach to address these issues is to assay large numbers of compounds against the target, either in a random or sometimes targeted fashion, a process
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Raychaudhuri, Soumya. "Text-Based Analysis of a Single Series of Gene Expression Measurements." In Computational Text Analysis. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780198567400.003.0012.

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In this chapter we begin to address the issue of the analysis of gene expression data with the scientific literature. Here we describe methods for the analysis of a single experiment—one where a single expression measurement has been made for many genes within the same organism. In Chapter 7 we will address the analysis of larger data sets with multiple expression measurements for each of the genes; the questions that occur in that setting are often more complex and utilization of scientific text in that setting can be more useful. But focusing on a single series of expression measurements is
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Sinsabaugh, Robert L., Michael J. Klug, Harold P. Collins, Phillip E. Yeager, and Søren O. Petersen. "Characterizing Soil Microbial Communities." In Standard Soil Methods for Long-Term Ecological Research. Oxford University PressNew York, NY, 1999. http://dx.doi.org/10.1093/oso/9780195120837.003.0016.

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Abstract The soil microbial community is intimately linked to primary production, soil structure, and biogeochemical cycling. The analyses described in this chapter provide structural or functional information about the soil microbiota beyond that provided by integrative measures of biomass or respiration. These methods of community analysis can be separated into two categories: those that generate phenotypic data and those that generate genotypic data {Fig. 16.1). The former includes lipid analysis, substrate utilization profiles, and extracellular enzyme activity assays. The latter includes
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Goswami, Namrata. "Conclusion." In The Naga Ethnic Movement for a Separate Homeland. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780190121174.003.0012.

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The final chapter ends with my own vision and thoughts on the Naga armed movement as well as the Indian state’s dealing of the conflict. I offer my estimation on why the Naga armed movement sustained itself for so long (over 101 years) as well as the political ideology that added strength to it. I offer my view on some of the challenges that it faces including severe internal ethnic differences. I provide a snapshot of how the future will look like in these conflict-affected areas post-the Naga framework agreement. I finally end with how Po has turned out in his life, 22 years after that day i
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Conference papers on the topic "SNaPshot assay"

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Cho, Dong-Keun, GwangMin Sun, JongWon Choi, Donghyeun Hwang, Hak-Soo Kim, and Tae-Won Hwang. "Verification of Source Term Analysis System for Decommissioning Wastes From a CANDU Reactor." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40202.

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There are now twenty commercial nuclear power reactors operating as of May 2010 in South Korea. As nuclear capacity becomes higher and installations age, the Korean government and industry have launched R&amp;D to estimate appropriate decommissioning costs of power reactors. In this paper, MCNP/ORIGEN2 code system which is being developed as a source term evaluation tool was verified by comparing the estimated nuclide inventory from MCNP/ORIGEN2 simulation with the measured nuclide inventory from chemical assay in an irradiated pressure tube discharged from Wolsong Unit 1 in 1994. Equilibrium
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Dickerson, W. Matthew, Edward M. Alderman, Lee Ann Beausang, Kristen Leong, and Ashley Saab. "Abstract 234: Snapshot of MAP kinase and related signal transduction pathways from biopsied cells using a novel non-optical assay technology - a proof of concept study." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-234.

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Whited, Bryce M., Matthias C. Hofmann, Chris G. Rylander, et al. "Non-Destructive Real-Time Imaging of Cell Seeded Tissue Engineered Scaffolds." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53721.

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The use of tissue engineered scaffolds in combination with progenitor cells has emerged as a promising strategy to restore or replace tissues damaged by disease or trauma. In addition to being biocompatible and exhibiting appropriate mechanical properties, scaffolds must be designed to sustain cell attachment, proliferation, and differentiation to ultimately produce the desired tissue once implanted in the patient [1]. Conventional techniques used to assess successful scaffold design include cell viability stains, DNA assays, and histological sectioning/staining. While significant information
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You might also be interested in the extended bibliographies on the topic 'SNaPshot assay' for particular source types:
Journal articles
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