Добірка наукової літератури з теми "Tumour sequencing"
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Статті в журналах з теми "Tumour sequencing"
Oey, Harald, Marissa Daniels, Vandana Relan, Tian Mun Chee, Morgan R. Davidson, Ian A. Yang, Jonathan J. Ellis, Kwun M. Fong, Lutz Krause, and Rayleen V. Bowman. "Whole-genome sequencing of human malignant mesothelioma tumours and cell lines." Carcinogenesis 40, no. 6 (April 25, 2019): 724–34. http://dx.doi.org/10.1093/carcin/bgz066.
Повний текст джерелаLolkema, M. P. "Platforms for Tumour Sequencing: Pertinence and Practicability." Annals of Oncology 25 (September 2014): iv9. http://dx.doi.org/10.1093/annonc/mdu294.2.
Повний текст джерелаNavin, Nicholas, Jude Kendall, Jennifer Troge, Peter Andrews, Linda Rodgers, Jeanne McIndoo, Kerry Cook, et al. "Tumour evolution inferred by single-cell sequencing." Nature 472, no. 7341 (March 13, 2011): 90–94. http://dx.doi.org/10.1038/nature09807.
Повний текст джерелаMuers, Mary. "Sequencing to detect tumour DNA in circulation." Nature Reviews Genetics 14, no. 1 (December 18, 2012): 4. http://dx.doi.org/10.1038/nrg3397.
Повний текст джерелаTang, Ka-Wei, and Erik Larsson. "Tumour virology in the era of high-throughput genomics." Philosophical Transactions of the Royal Society B: Biological Sciences 372, no. 1732 (September 11, 2017): 20160265. http://dx.doi.org/10.1098/rstb.2016.0265.
Повний текст джерелаde Ruiter, J. R., L. F. A. Wessels, and J. Jonkers. "Mouse models in the era of large human tumour sequencing studies." Open Biology 8, no. 8 (August 2018): 180080. http://dx.doi.org/10.1098/rsob.180080.
Повний текст джерелаPatel, Areeba, Helin Dogan, Alexander Jung, Zaira Seferbekova, Alexander Payne, Michael Ritter, Daniel Schrimpf, et al. "PATH-46. COMPUTATIONAL HISTOPATHOLOGY INFORMED RAPID TARGETED NANOPORE SEQUENCING ENABLES AFFORDABLE NEXT DAY REPORTING OF COMPREHENSIVE MOLECULAR MARKERS FOR CNS TUMOUR DIAGNOSTICS." Neuro-Oncology 24, Supplement_7 (November 1, 2022): vii161. http://dx.doi.org/10.1093/neuonc/noac209.619.
Повний текст джерелаKnudsen, Erik S., Uthra Balaji, Brian Mannakee, Paris Vail, Cody Eslinger, Christopher Moxom, John Mansour, and Agnieszka K. Witkiewicz. "Pancreatic cancer cell lines as patient-derived avatars: genetic characterisation and functional utility." Gut 67, no. 3 (January 10, 2017): 508–20. http://dx.doi.org/10.1136/gutjnl-2016-313133.
Повний текст джерелаStankunaite, Reda, Sally L. George, Lewis Gallagher, Sabri Jamal, Ridwan Shaikh, Lina Yuan, Debbie Hughes, et al. "Circulating tumour DNA sequencing to determine therapeutic response and identify tumour heterogeneity in patients with paediatric solid tumours." European Journal of Cancer 162 (February 2022): 209–20. http://dx.doi.org/10.1016/j.ejca.2021.09.042.
Повний текст джерелаTanner, Georgette, David R. Westhead, Alastair Droop, and Lucy F. Stead. "Simulation of heterogeneous tumour genomes with HeteroGenesis and in silico whole exome sequencing." Bioinformatics 35, no. 16 (January 4, 2019): 2850–52. http://dx.doi.org/10.1093/bioinformatics/bty1063.
Повний текст джерелаДисертації з теми "Tumour sequencing"
Burns, Alice Sin Ying Wai. "The role of the p53 tumour suppressor pathway in central primitive neuroectodermal tumours." Thesis, University of Newcastle Upon Tyne, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300357.
Повний текст джерелаDuarte, Antonio. "Regulation of gene expression by the Wilms' tumour suppressor, WT1." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389178.
Повний текст джерелаMurtaza, Muhammed. "Identification and monitoring of somatic mutations in solid cancers by sequencing circulating tumour DNA." Thesis, University of Cambridge, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708647.
Повний текст джерелаRoss, Edith. "Inferring tumour evolution from single-cell and multi-sample data." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/274604.
Повний текст джерелаFewings, Eleanor Rose. "The use of whole exome sequencing data to identify candidate genes involved in cancer and benign tumour predisposition." Thesis, University of Cambridge, 2019. https://www.repository.cam.ac.uk/handle/1810/285963.
Повний текст джерелаAsante, Du-Bois. "Development and evaluation of methodologies for analysis of CTC and ctDNA in patients with ovarian carcinoma." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2022. https://ro.ecu.edu.au/theses/2570.
Повний текст джерелаNaven, Marc. "Development of a pipeline and protocols for next generation sequencing of blood and formalin-fixed, paraffin-embedded tumour DNA samples." Thesis, Cardiff University, 2015. http://orca.cf.ac.uk/91435/.
Повний текст джерелаBucher, Katharina M. I. "The tumour suppressor gene p53 in the horse : identification, cloning and sequencing : its possible role in the pathogenesis of equine sarcoid /." [S.l.] : [s.n.], 1995. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Повний текст джерелаChoudhry, Hani. "Genome-wide analysis of the hypoxic breast cancer transcriptome using next generation sequencing." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:9a66b553-a66c-4164-a854-5881be65ca45.
Повний текст джерелаStrakova, Andrea. "Genome diversity and evolution in canine transmissible venereal tumour." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/276037.
Повний текст джерелаКниги з теми "Tumour sequencing"
Maher, Christopher J., and Elaine R. Mardis. Genomic Landscape of Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0004.
Повний текст джерелаRamaswamy, Vijay, Jason T. Huse, and Yasmin Khakoo. Pediatric Brain Tumors. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0140.
Повний текст джерелаWu, Wei, and Hani Choudhry. Next Generation Sequencing in Cancer Research Vol. 1 : Volume 1: Decoding the Cancer Genome. Springer London, Limited, 2013.
Знайти повний текст джерелаTangen, Catherine M., Marian L. Neuhouser, and Janet L. Stanford. Prostate Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0053.
Повний текст джерелаPezzella, Francesco, Mahvash Tavassoli, and David J. Kerr, eds. Oxford Textbook of Cancer Biology. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780198779452.001.0001.
Повний текст джерелаЧастини книг з теми "Tumour sequencing"
Subramanian, Ayshwarya, Stanley Shackney, and Russell Schwartz. "Tumor Phylogenetics in the NGS Era: Strategies, Challenges, and Future Prospects." In Next Generation Sequencing in Cancer Research, 335–57. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7645-0_17.
Повний текст джерелаSu, Xiaoping, Gabriel G. Malouf, and Francisco J. Esteva. "Impact and Challenges in Assessing Tumor Purity by Next-Generation Sequencing." In Next Generation Sequencing in Cancer Research, 359–71. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7645-0_18.
Повний текст джерелаMarass, Francesco, Francesc Castro-Giner, Barbara Maria Szczerba, Katharina Jahn, Jack Kuipers, Nicola Aceto, and Niko Beerenwinkel. "Computational Analysis of DNA and RNA Sequencing Data Obtained from Liquid Biopsies." In Tumor Liquid Biopsies, 347–68. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-26439-0_18.
Повний текст джерелаWatson, Geoffrey Alan, Kirsty Taylor, and Lillian L. Siu. "Innovation and Advances in Precision Medicine in Head and Neck Cancer." In Critical Issues in Head and Neck Oncology, 355–73. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63234-2_24.
Повний текст джерелаSweeney, Robert T., and Matt van de Rijn. "Microarrays and High-Throughput Sequencing in Desmoid-Type Fibromatosis and Scar." In Desmoid Tumors, 181–93. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1685-8_12.
Повний текст джерелаSmith, C. C., L. M. Bixby, K. L. Miller, S. R. Selitsky, D. S. Bortone, K. A. Hoadley, B. G. Vincent, and J. S. Serody. "Using RNA Sequencing to Characterize the Tumor Microenvironment." In Biomarkers for Immunotherapy of Cancer, 245–72. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9773-2_12.
Повний текст джерелаVilimas, Tomas. "Measuring Tumor Mutational Burden Using Whole-Exome Sequencing." In Biomarkers for Immunotherapy of Cancer, 63–91. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9773-2_3.
Повний текст джерелаWang, Jinhua. "Tumor Sequencing: Enabling Personalized Targeted Treatments with Informatics." In Health Informatics, 161–74. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-18626-5_11.
Повний текст джерелаQu, Kunbin, Joffre Baker, and Yan Ma. "Applications of NGS to Screen FFPE Tumours for Detecting Fusion Transcripts." In Next Generation Sequencing in Cancer Research, Volume 2, 155–77. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15811-2_10.
Повний текст джерелаChen, Mengjie, Lin Hou, and Hongyu Zhao. "Statistical Methods for the Analysis of Next Generation Sequencing Data from Paired Tumor-Normal Samples." In Statistical Analysis of Next Generation Sequencing Data, 379–404. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07212-8_19.
Повний текст джерелаТези доповідей конференцій з теми "Tumour sequencing"
Roze, JF, GM Monroe, JW Groeneweg, E. Stelloo, ST Paijens, HW Nijman, HS van Meurs, et al. "Whole genome sequencing of ovarian granulosa cell tumours show heterogeneity, genomic instability and tumour evolution." In ESGO Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-esgo.27.
Повний текст джерелаShinde, Pravin V., Rajesh Deshmukh, and Preeti S. Patil. "Design of Deep Learning Approach for Expression of Genes by Tumour RNA-Sequencing Data." In 2022 IEEE 7th International conference for Convergence in Technology (I2CT). IEEE, 2022. http://dx.doi.org/10.1109/i2ct54291.2022.9825178.
Повний текст джерелаKoo, Si-Lin, Joe Poh Sheng Yeong, Andy Nguyen, Clarinda Wei Ling Chua, J. Zachary Sanborn, Steve Benz, Wah Siew Tan, et al. "Abstract 5725: Systematic identification of tumour-specific neoantigens(by whole-genome sequencing) and correlation between tumour neoantigen burden, PD-L1 expression and immune infiltrates in 158Asian colorectal cancers." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-5725.
Повний текст джерелаPeeters, Dieter JE, Ken Op De Beeck, Anja Brouwer, Geert Vandeweyer, Patrick Pauwels, Marc Peeters, Peter B. Vermeulen, et al. "Abstract P4-01-14: Whole exome sequencing of circulating and disseminated tumour cells in patients with metastatic breast cancer." In Thirty-Seventh Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 9-13, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.sabcs14-p4-01-14.
Повний текст джерелаSilva, Harini de, Niko Thio, Piers Blombery, Ella Thompson, Anand Deva, Miles Prince, Paul Neeson, and Criselle DSouza. "1442 Investigating the tumour immune microenvironment of breast implant associated anaplastic large cell lymphoma using single cell RNA sequencing." In SITC 37th Annual Meeting (SITC 2022) Abstracts. BMJ Publishing Group Ltd, 2022. http://dx.doi.org/10.1136/jitc-2022-sitc2022.1442.
Повний текст джерелаMukhopadhyay, Asima, Nicola Curtin, and Richard Edmondson. "Evaluation of different methods to assess homologous recombination status and sensitivity to PARP inhibitors in ovarian cancer." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685289.
Повний текст джерелаPeeters, DJE, P. Kumar, N. Van der Aa, F. Rothé, K. Theunis, K. Op de Beeck, SJ Van Laere, et al. "Abstract P1-04-03: Genome-wide analysis of copy number variations and mutation profiles of single circulating tumour cells using massively parallel paired-end sequencing." In Abstracts: Thirty-Sixth Annual CTRC-AACR San Antonio Breast Cancer Symposium - Dec 10-14, 2013; San Antonio, TX. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/0008-5472.sabcs13-p1-04-03.
Повний текст джерелаDe Laere, Bram, Dieter JE Peeters, Salgado Roberto, Vermeulen B. Peter, Van Dam A. Peter, Dirix Y. Luc, and Van Laere J. Steven. "Abstract P4-01-09: Exploring the intra-patientPIK3CAmutational heterogeneity of circulating tumour cells by massive parallel sequencing in patients with metastatic hormone receptor-positive breast cancer." In Thirty-Seventh Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 9-13, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.sabcs14-p4-01-09.
Повний текст джерелаLinch, E., L. Miller, T. Looney, A. Zheng, D. Topacio-Hall, G. Nistala, G. Lowman, F. Hyland, and M. Andersen. "PO-394 Performance of a targeted T cell receptor beta immune repertoire sequencing panel in several FFPE tissue types – a tool for interrogation of the tumour microenvironment." In Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.906.
Повний текст джерелаBaird, Richard D., Lucy Kilburn, Sarah Kernaghan, Andrew M. Wardley, Iain Macpherson, Rebecca Roylance, Peter Stephens, et al. "Abstract P1-19-14: Results from plasmaMATCH trial treatment cohort D: A phase II trial of capivasertib in patients with an AKT activation basket mutation identified via ctDNA testing or tumour sequencing (CRUK/15/010)." In Abstracts: 2019 San Antonio Breast Cancer Symposium; December 10-14, 2019; San Antonio, Texas. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.sabcs19-p1-19-14.
Повний текст джерелаЗвіти організацій з теми "Tumour sequencing"
Wagle, Nikhil. Tumor Genomic Profiling in Breast Cancer Patients Using Targeted Massively Parallel Sequencing. Fort Belvoir, VA: Defense Technical Information Center, January 2014. http://dx.doi.org/10.21236/ada598724.
Повний текст джерелаCooney, Kathleen A. High Throughput Sequencing of Germline and Tumor from Men With Early-Onset Metastatic Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada611828.
Повний текст джерелаCooney, Kathleen A. High-Throughput Sequencing of Germline and Tumor From Men with Early-Onset Metastatic Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2015. http://dx.doi.org/10.21236/ada624260.
Повний текст джерела