المؤلفون: Karin Hellner, Fabrizio Miranda, Donatien Fotso Chedom, Sandra Herrero-Gonzalez, Daniel M. Hayden, Rick Tearle, Mara Artibani, Mohammad KaramiNejadRanjbar, Ruth Williams, Kezia Gaitskell, Samar Elorbany, Ruoyan Xu, Alex Laios, Petronela Buiga, Karim Ahmed, Sunanda Dhar, Rebecca Yu Zhang, Leticia Campo, Kevin A. Myers, María Lozano, María Ruiz-Miró, Sónia Gatius, Alba Mota, Gema Moreno-Bueno, Xavier Matias-Guiu, Javier Benítez, Lorna Witty, Gil McVean, Simon Leedham, Ian Tomlinson, Radoje Drmanac, Jean-Baptiste Cazier, Robert Klein, Kevin Dunne, Robert C. Bast Jr, Stephen H. Kennedy, Bassim Hassan, Stefano Lise, María José Garcia, Brock A. Peters, Christopher Yau, Tatjana Sauka-Spengler, Ahmed Ashour Ahmed

المصدر: EBioMedicine, Vol 10, Iss C, Pp 137-149 (2016)

مصطلحات موضوعية: Ovarian cancer, Fallopian tube, BRCA mutations, SOX2, Screening, Precancer, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S235239641630305X; https://doaj.org/toc/2352-3964

URL الوصول: https://doaj.org/article/48848af61fb0476781413217637a8181

المؤلفون: Brock A. Peters, Radoje Drmanac, John W. Park, Hope S. Rugo, Snezana Drmanac, Emily Park, Rick Tearle, Katharine Lee, Rebecca Yu Zhang, Yuxiang Li, Xingpeng Chen, Yanxiang Chen, Zhenyu Li, Serban Ciotlos, Qing Mao, Daniel M. Hayden, Jia Liu, Xuhao Luo, Misha R. Agarwal, Robert Chin, Mark Jesus M. Magbanua, Natali Gulbahce

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5568c9096d7e07789f964b7c311c05
https://doi.org/10.1158/0008-5472.22414221.v1

المؤلفون: Brock A. Peters, Radoje Drmanac, John W. Park, Hope S. Rugo, Snezana Drmanac, Emily Park, Rick Tearle, Katharine Lee, Rebecca Yu Zhang, Yuxiang Li, Xingpeng Chen, Yanxiang Chen, Zhenyu Li, Serban Ciotlos, Qing Mao, Daniel M. Hayden, Jia Liu, Xuhao Luo, Misha R. Agarwal, Robert Chin, Mark Jesus M. Magbanua, Natali Gulbahce

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a365a7eaa995fdbc9826b100b175fd
https://doi.org/10.1158/0008-5472.22414209

المؤلفون: Brock A. Peters, Radoje Drmanac, John W. Park, Hope S. Rugo, Snezana Drmanac, Emily Park, Rick Tearle, Katharine Lee, Rebecca Yu Zhang, Yuxiang Li, Xingpeng Chen, Yanxiang Chen, Zhenyu Li, Serban Ciotlos, Qing Mao, Daniel M. Hayden, Jia Liu, Xuhao Luo, Misha R. Agarwal, Robert Chin, Mark Jesus M. Magbanua, Natali Gulbahce

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32260f32c03c33f6ba686ff35f3d98f5
https://doi.org/10.1158/0008-5472.22414206

المؤلفون: Brock A. Peters, Radoje Drmanac, John W. Park, Hope S. Rugo, Snezana Drmanac, Emily Park, Rick Tearle, Katharine Lee, Rebecca Yu Zhang, Yuxiang Li, Xingpeng Chen, Yanxiang Chen, Zhenyu Li, Serban Ciotlos, Qing Mao, Daniel M. Hayden, Jia Liu, Xuhao Luo, Misha R. Agarwal, Robert Chin, Mark Jesus M. Magbanua, Natali Gulbahce

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e7ebe8a6667c7d5906fcaff99801aa4
https://doi.org/10.1158/0008-5472.c.6508917.v1

المؤلفون: Erin E. Peters, Zhenyu Li, Natali Gulbahce, Wenwei Zhang, Rebecca Yu Zhang, Radoje Drmanac, Robert Chin, Huixin Xu, Yuqing Deng, Weiwei Xie, Fang Chen, Qing Mao, Quan Shi, Brock A. Peters

المصدر: Clinical Chemistry. 64:715-725

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Amniotic fluid, DNA Copy Number Variations, Autism Spectrum Disorder, Clinical Biochemistry, Genomics, Computational biology, Biology, medicine.disease_cause, Genome, Cohort Studies, 03 medical and health sciences, chemistry.chemical_compound, Fetus, medicine, Humans, Abnormalities, Multiple, Genetic Predisposition to Disease, Gene, Whole genome sequencing, Mutation, Whole Genome Sequencing, medicine.diagnostic_test, Genome, Human, Biochemistry (medical), Amniotic Fluid, 030104 developmental biology, chemistry, Amniocentesis, Feasibility Studies, Female, Eyebrows, Darier Disease, DNA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::389eb6f1c592237e43e69f9508d78a20
https://doi.org/10.1373/clinchem.2017.281220

المؤلفون: Xiao Liu, Rebecca Yu Zhang, Yan Zou, Chongjun Xu, Nina Barua, Ou Wang, Han K. Lam, Xun Xu, Jingbo Tang, Yujun Zhou, Jing Wang, Yinlong Xie, Xiaofang Cheng, Brock A. Peters, Wenlan Tian, Jingwan Wang, Fei Fan, Dan Chen, Jia Sophie Liu, Ao Chen, Snezana Drmanac, Andrei Alexeev, Yuhui Sun, Linying Wang, Radoje Drmanac, Ellis Anderson, Xiaojuan Qi, Dong Yuliang, Wenwei Zhang, M. Wu, Robert Chin, Huanming Yang, Qing Mao, Christian Villarosa, Karsten Kristiansen, Staci Nguyen, Scott Gablenz, He Wang, Darlene Nguyen

المصدر: Wang, O, Chin, R, Cheng, X, Wu, M K Y, Mao, Q, Tang, J, Sun, Y, Anderson, E, Lam, H K, Chen, D, Zhou, Y, Wang, L, Fan, F, Zou, Y, Xie, Y, Zhang, R Y, Drmanac, S, Nguyen, D, Xu, C, Villarosa, C, Gablenz, S, Barua, N, Nguyen, S, Tian, W, Liu, J S, Wang, J, Liu, X, Qi, X, Chen, A, Wang, H, Dong, Y, Zhang, W, Alexeev, A, Yang, H, Wang, J, Kristiansen, K, Xu, X, Drmanac, R & Peters, B A 2019, ' Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly ', Genome Research, vol. 29, no. 5, pp. 798-808 . https://doi.org/10.1101/gr.245126.118

مصطلحات موضوعية: Cost-Benefit Analysis, Method, Sequence assembly, Genomics, Computational biology, Biology, Barcode, Genome, DNA sequencing, law.invention, 03 medical and health sciences, 0302 clinical medicine, law, Genetics, Humans, Genomic library, Genetics (clinical), Gene Library, 030304 developmental biology, 0303 health sciences, Whole Genome Sequencing, Genome, Human, High-Throughput Nucleotide Sequencing, Diploidy, genomic DNA, Haplotypes, Human genome, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f6de987fdf799d1cbdb17c1b96eee50
https://curis.ku.dk/portal/da/publications/efficient-and-unique-cobarcoding-of-secondgeneration-sequencing-reads-from-long-dna-molecules-enabling-costeffective-and-accurate-sequencing-haplotyping-and-de-novo-assembly(17bcf649-f5eb-48d0-b4a6-5250b87c3764).html

المؤلفون: Mindy K. Graham, Ming Yuan, Christine Davis, David M. Esopi, Christopher M. Heaphy, Rebecca Yu Zhang, Charles G. Eberhart, Jacqueline A. Brosnan-Cashman, Alan K. Meeker, Anthony J. Rizzo, Eric H. Raabe, Kaylar M. Myers

المصدر: PLoS ONE
PLoS ONE, Vol 13, Iss 9, p e0204159 (2018)

مصطلحات موضوعية: 0301 basic medicine, Telomerase, lcsh:Medicine, DNA cloning, Artificial Gene Amplification and Extension, medicine.disease_cause, Polymerase Chain Reaction, Medicine and Health Sciences, lcsh:Science, Neurological Tumors, Cultured Tumor Cells, Mutation, Multidisciplinary, Chromosome Biology, Glioma, Telomere, Chromatin, Telomeres, Phenotype, Oncology, Neurology, Biological Cultures, Research Article, Chromosome Structure and Function, X-linked Nuclear Protein, Immunoblotting, Molecular Probe Techniques, Context (language use), Biology, Research and Analysis Methods, Chromatin remodeling, Chromosomes, 03 medical and health sciences, Cell Line, Tumor, medicine, Humans, Epigenetics, Molecular Biology Techniques, Molecular Biology, ATRX, lcsh:R, DNA Helicases, Biology and Life Sciences, Cancers and Neoplasms, Telomere Homeostasis, Cell Biology, Cell Cultures, Vector Cloning, Glioma Cells, 030104 developmental biology, Cancer research, lcsh:Q, Cloning

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b8a6ed903bd0dcd8d941e8535eef76
http://europepmc.org/articles/PMC6143253

المؤلفون: Ou Wang, Robert Chin, Xiaofang Cheng, Michelle Ka Wu, Qing Mao, Jingbo Tang, Yuhui Sun, Ellis Anderson, Han K. Lam, Dan Chen, Yujun Zhou, Linying Wang, Fei Fan, Yan Zou, Yinlong Xie, Rebecca Yu Zhang, Snezana Drmanac, Darlene Nguyen, Chongjun Xu, Christian Villarosa, Scott Gablenz, Nina Barua, Staci Nguyen, Wenlan Tian, Jia Sophie Liu, Jingwan Wang, Xiao Liu, Xiaojuan Qi, Ao Chen, He Wang, Yuliang Dong, Wenwei Zhang, Andrei Alexeev, Huanming Yang, Jian Wang, Karsten Kristiansen, Xun Xu, Radoje Drmanac, Brock A. Peters

مصطلحات موضوعية: Whole genome sequencing, Contig, Computer science, Library preparation, Haplotype, Sequence assembly, Computational biology, Genome, DNA sequencing, genomic DNA, chemistry.chemical_compound, chemistry, Human genome, Ploidy, DNA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::898d8507337eb7fb1b962e68dac5dc7c

المؤلفون: R. Prates, Radoje Drmanac, Birgit Crain, Misha R. Agarwal, Brock A. Peters, Oleg Alferov, Mark A. McElwain, Rebecca Yu Zhang, Daniel M. Hayden, Rick Tearle, Natali Gulbahce, Alan S. Berkeley, Y. Tom Tang, Santiago Munné, Bahram Ghaffarzadeh Kermani

المصدر: Genome Research. 25:426-434

مصطلحات موضوعية: Heterozygote, Method, Fertilization in Vitro, Biology, Preimplantation genetic diagnosis, Polymorphism, Single Nucleotide, Genome, Deep sequencing, chemistry.chemical_compound, Genetics, Humans, Point Mutation, Indel, Genetics (clinical), Sequence Deletion, Whole genome sequencing, Genome, Human, Point mutation, Haplotype, High-Throughput Nucleotide Sequencing, Exons, Embryo, Mammalian, Blastocyst, Haplotypes, chemistry, DNA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e82b6f198efdba3898b1461de08cb90b
https://doi.org/10.1101/gr.181255.114