Journal articles on the topic 'High-density genotyping microarray'
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Huang, Joe Xi, Dorothy Mehrens, Rick Wiese, Sandy Lee, Sun W. Tam, Steve Daniel, James Gilmore, Michael Shi, and Deval Lashkari. "High-Throughput Genomic and Proteomic Analysis Using Microarray Technology." Clinical Chemistry 47, no. 10 (October 1, 2001): 1912–16. http://dx.doi.org/10.1093/clinchem/47.10.1912.
Full textSansaloni, Carolina P., César D. Petroli, Jason Carling, Corey J. Hudson, Dorothy A. Steane, Alexander A. Myburg, Dario Grattapaglia, René E. Vaillancourt, and Andrzej Kilian. "A high-density Diversity Arrays Technology (DArT) microarray for genome-wide genotyping in Eucalyptus." Plant Methods 6, no. 1 (2010): 16. http://dx.doi.org/10.1186/1746-4811-6-16.
Full textDacheux, Laurent, Nicolas Berthet, Gabriel Dissard, Edward C. Holmes, Olivier Delmas, Florence Larrous, Ghislaine Guigon, et al. "Application of Broad-Spectrum Resequencing Microarray for Genotyping Rhabdoviruses." Journal of Virology 84, no. 18 (July 7, 2010): 9557–74. http://dx.doi.org/10.1128/jvi.00771-10.
Full textDesjardins, Christopher A., Jürgen Gadau, Jacqueline A. Lopez, Oliver Niehuis, Amanda R. Avery, David W. Loehlin, Stephen Richards, John K. Colbourne, and John H. Werren. "Fine-Scale Mapping of the Nasonia Genome to Chromosomes Using a High-Density Genotyping Microarray." G3: Genes|Genomes|Genetics 3, no. 2 (February 2013): 205–15. http://dx.doi.org/10.1534/g3.112.004739.
Full textJasmine, F., H. Ahsan, I. L. Andrulis, E. M. John, J. Chang-Claude, and M. G. Kibriya. "Whole-Genome Amplification Enables Accurate Genotyping for Microarray-Based High-Density Single Nucleotide Polymorphism Array." Cancer Epidemiology Biomarkers & Prevention 17, no. 12 (December 1, 2008): 3499–508. http://dx.doi.org/10.1158/1055-9965.epi-08-0482.
Full textHans, Aymeric, Delphine Gaudaire, Jean-Claude Manuguerra, Albertine Leon, Antoine Gessain, Claire Laugier, Nicolas Berthet, and Stephan Zientara. "Combination of an Unbiased Amplification Method and a Resequencing Microarray for Detecting and Genotyping Equine Arteritis Virus." Journal of Clinical Microbiology 53, no. 1 (October 22, 2014): 287–91. http://dx.doi.org/10.1128/jcm.01935-14.
Full textLi, Honghua, Hui-Yun Wang, Danielle Greenawalt, Xiangfeng Cui, IrinaV Tereshchenko, Minjie Luo, Qifeng Yang, et al. "Identification of possible genetic alterations in the breast cancer cell line MCF-7 using high-density SNP genotyping microarray." Journal of Carcinogenesis 8, no. 1 (2009): 6. http://dx.doi.org/10.4103/1477-3163.50886.
Full textVogler, Amy J., Dawn Birdsell, Lance B. Price, Jolene R. Bowers, Stephen M. Beckstrom-Sternberg, Raymond K. Auerbach, James S. Beckstrom-Sternberg, et al. "Phylogeography of Francisella tularensis: Global Expansion of a Highly Fit Clone." Journal of Bacteriology 191, no. 8 (February 27, 2009): 2474–84. http://dx.doi.org/10.1128/jb.01786-08.
Full textOhlson, Erik W., and Michael P. Timko. "Mapping and Validation of Alectra vogelii Resistance in the Cowpea Landrace B301." Agronomy 12, no. 11 (October 27, 2022): 2654. http://dx.doi.org/10.3390/agronomy12112654.
Full textBjörkholm, Britta, Annelie Lundin, Anna Sillén, Karen Guillemin, Nina Salama, Carlos Rubio, Jeffrey I. Gordon, Per Falk, and Lars Engstrand. "Comparison of Genetic Divergence and Fitness between Two Subclones of Helicobacter pylori." Infection and Immunity 69, no. 12 (December 1, 2001): 7832–38. http://dx.doi.org/10.1128/iai.69.12.7832-7838.2001.
Full textBlades, Matthew, Jamie Freyer, Jonas Donner, Rebecca Chodroff Foran, and Oliver P. Forman. "Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs." PLOS ONE 17, no. 5 (May 26, 2022): e0267604. http://dx.doi.org/10.1371/journal.pone.0267604.
Full textTakita, Junko, Motohiro Kato, Fumihiko Nakamura, Yuyan Chen, Go Yamamoto, Yasuhito Nannya, Masashi Sanada, et al. "High-Resolution Analyses of Genetic and Epigenetic Aberrations in Infant Leukemia with MLL Rearrangement." Blood 110, no. 11 (November 16, 2007): 4238. http://dx.doi.org/10.1182/blood.v110.11.4238.4238.
Full textKato-Maeda, Midori, Jeanne T. Rhee, Thomas R. Gingeras, Hugh Salamon, Jorg Drenkow, Nat Smittipat, and Peter M. Small. "Comparing Genomes within the Species Mycobacterium tuberculosis." Genome Research 11, no. 4 (April 1, 2001): 547–54. http://dx.doi.org/10.1101/gr166401.
Full textSearles Quick, Veronica B., Belinda Wang, and Matthew W. State. "Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders." Neuropsychopharmacology 46, no. 1 (July 15, 2020): 55–69. http://dx.doi.org/10.1038/s41386-020-0768-y.
Full textReverter, A., E. K. F. Chan, S. A. Lehnert, W. Barris, S. M. McWilliam, B. P. Dalrymple, and W. Barendse. "Dissection of beef quality phenotypes using a myogenin network-anchored systems biology approach." Australian Journal of Experimental Agriculture 48, no. 8 (2008): 1053. http://dx.doi.org/10.1071/ea08052.
Full textKim, Dong Hwan (Dennis), Boram Han, Kyusang Lee, TaeJin Ahn, Dae-soon Son, Insuk Sohn, Sin-Ho Jung, et al. "Pharmacogenomics-Based Drug Response Prediction Model for Acute Myeloid Leukemia with Normal Karyotype." Blood 116, no. 21 (November 19, 2010): 2698. http://dx.doi.org/10.1182/blood.v116.21.2698.2698.
Full textSanada, Masashi, Yasuhito Nannya, Kumi Nakazaki, Go Yamamoto, Lili Wang, Noriko Hosoya, Akira Hangaishi, Mineo Kurokawa, Shigeru Chiba, and Seishi Ogawa. "Genome-Wide Analysis of Copy Number Analysis of Myelodysplastic Syndromes Using High-Density SNP-Genotyping Microarrays." Blood 106, no. 11 (November 16, 2005): 3420. http://dx.doi.org/10.1182/blood.v106.11.3420.3420.
Full textSuzuki, Makoto, Motohiro Kato, Chen Yuyan, Junko Takita, Masashi Sanada, Yasuhito Nannya, Go Yamamoto, et al. "Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays." Cancer Science 99, no. 3 (March 2008): 564–70. http://dx.doi.org/10.1111/j.1349-7006.2007.00710.x.
Full textHomer, Nils, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V. Pearson, Dietrich A. Stephan, Stanley F. Nelson, and David W. Craig. "Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays." PLoS Genetics 4, no. 8 (August 29, 2008): e1000167. http://dx.doi.org/10.1371/journal.pgen.1000167.
Full textBorneman, Anthony R., Eveline J. Bartowsky, Jane McCarthy, and Paul J. Chambers. "Genotypic diversity in Oenococcus oeni by high-density microarray comparative genome hybridization and whole genome sequencing." Applied Microbiology and Biotechnology 86, no. 2 (January 29, 2010): 681–91. http://dx.doi.org/10.1007/s00253-009-2425-6.
Full textScionti, Francesca, Maria Di Martino, Licia Pensabene, Valentina Bruni, and Daniela Concolino. "The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders." High-Throughput 7, no. 3 (September 14, 2018): 28. http://dx.doi.org/10.3390/ht7030028.
Full textKato, Motohiro, Kumi Nakazaki, Kengo Takeuchi, Go Yamamoto, Yasuhito Nannya, Masashi Sanada, Satsuki Muto, et al. "Genomic Profiling of Different Subtypes of B-Cell Non-Hodgkin’s Lymphoma Using High-Density Single Nucleotide Polymorphism (SNP) Microarrays." Blood 110, no. 11 (November 16, 2007): 3588. http://dx.doi.org/10.1182/blood.v110.11.3588.3588.
Full textCamos, Mireia, Jordi Esteve, Dolors Colomer, Pedro Jares, Maria Rozman, Neus Villamor, Dolors Costa, et al. "Gene Expression Signature of Acute Myeloid Leukemia (AML) with T(8;16)(P11;P13) and MYST3-CREBBP Rearrangement: A Microarray Study Validated by Multiple Real-Time PCR." Blood 106, no. 11 (November 16, 2005): 3009. http://dx.doi.org/10.1182/blood.v106.11.3009.3009.
Full textPoznyak, Anastasia V., Andrey V. Grechko, Reinhard Wetzker, and Alexander N. Orekhov. "In Search for Genes Related to Atherosclerosis and Dyslipidemia Using Animal Models." International Journal of Molecular Sciences 21, no. 6 (March 18, 2020): 2097. http://dx.doi.org/10.3390/ijms21062097.
Full textPrzychodzen, Bartlomiej P., Andres Jerez, Hideki Makishima, Kathryn M. Guinta, and Peter Chomczynski. "Mass Screening for Non-Synonymous SNPs Using Custom Cancer Microarrays Directly Reveals Possible Pathogenic Predisposition Factors in AA." Blood 118, no. 21 (November 18, 2011): 1333. http://dx.doi.org/10.1182/blood.v118.21.1333.1333.
Full textSpivak, Jerry L., Chunfa Jie, Donna M. Williams, and Alison R. Moliterno. "Gender Counts: Defining the Core Genetic Profile of Polycythemia Vera." Blood 104, no. 11 (November 16, 2004): 660. http://dx.doi.org/10.1182/blood.v104.11.660.660.
Full textHuang, Meng, Muyi Liu, Hongmin Li, Jonathan King, Amy Smuts, Bruce Budowle, and Jianye Ge. "A machine learning approach for missing persons cases with high genotyping errors." Frontiers in Genetics 13 (October 3, 2022). http://dx.doi.org/10.3389/fgene.2022.971242.
Full textNguyen, Dat Thanh, Trang T. H. Tran, Mai Hoang Tran, Khai Tran, Duy Pham, Nguyen Thuy Duong, Quan Nguyen, and Nam S. Vo. "A comprehensive evaluation of polygenic score and genotype imputation performances of human SNP arrays in diverse populations." Scientific Reports 12, no. 1 (October 20, 2022). http://dx.doi.org/10.1038/s41598-022-22215-y.
Full textErickson, Stephen W., Stewart L. MacLeod, and Charlotte A. Hobbs. "Cheek swabs, SNP chips, and CNVs: Assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray." BMC Medical Genetics 13, no. 1 (June 26, 2012). http://dx.doi.org/10.1186/1471-2350-13-51.
Full textBelloy, Michael E., Sarah J. Eger, Yann Le Guen, Vincent Damotte, Shahzad Ahmad, M. Arfan Ikram, Alfredo Ramirez, et al. "Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping." Alzheimer's Research & Therapy 14, no. 1 (February 4, 2022). http://dx.doi.org/10.1186/s13195-022-00962-4.
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