Статті в журналах з теми "Tumour sequencing"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Tumour sequencing".
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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 джерелаRico, Karen, Suzann Duan, Ritu L. Pandey, Yuliang Chen, Jayati T. Chakrabarti, Julie Starr, Yana Zavros, et al. "Genome analysis identifies differences in the transcriptional targets of duodenal versus pancreatic neuroendocrine tumours." BMJ Open Gastroenterology 8, no. 1 (November 2021): e000765. http://dx.doi.org/10.1136/bmjgast-2021-000765.
Повний текст джерелаChong, Irene Y., Naureen Starling, Alistair Rust, John Alexander, Lauren Aronson, Marta Llorca-Cardenosa, Ritika Chauhan, et al. "The Mutational Concordance of Fixed Formalin Paraffin Embedded and Fresh Frozen Gastro-Oesophageal Tumours Using Whole Exome Sequencing." Journal of Clinical Medicine 10, no. 2 (January 9, 2021): 215. http://dx.doi.org/10.3390/jcm10020215.
Повний текст джерелаChong, Irene Y., Naureen Starling, Alistair Rust, John Alexander, Lauren Aronson, Marta Llorca-Cardenosa, Ritika Chauhan, et al. "The Mutational Concordance of Fixed Formalin Paraffin Embedded and Fresh Frozen Gastro-Oesophageal Tumours Using Whole Exome Sequencing." Journal of Clinical Medicine 10, no. 2 (January 9, 2021): 215. http://dx.doi.org/10.3390/jcm10020215.
Повний текст джерелаMarziali, Andre. "Sensitive detection of tumor nucleic acids in plasma by mutation-enriched next generation sequencing." Journal of Clinical Oncology 31, no. 15_suppl (May 20, 2013): e22041-e22041. http://dx.doi.org/10.1200/jco.2013.31.15_suppl.e22041.
Повний текст джерелаNagaraju, Santhosh, Ion Boiangiu, Ian Brown, Hussien El-Maghraby, and U. Pohl. "Intracranial myxoid mesenchymal tumour with EWSR1-ATF1 fusion mimicking high grade glioma." Neuro-Oncology 23, Supplement_4 (October 1, 2021): iv23—iv24. http://dx.doi.org/10.1093/neuonc/noab195.059.
Повний текст джерелаSmyth, Robert J., Valentina Thomas, Joanna Fay, Ronan Ryan, Siobhan Nicholson, Ross K. Morgan, Liam Grogan, et al. "Tumour Genome Characterization of a Rare Case of Pulmonary Enteric Adenocarcinoma and Prior Colon Adenocarcinoma." Journal of Personalized Medicine 11, no. 8 (August 4, 2021): 768. http://dx.doi.org/10.3390/jpm11080768.
Повний текст джерелаCastignani, Carla, Jonas Demeulemeester, Elizabeth Larose Cadieux, Robert E. Hynds, David R. Pearce, Stefan C. Dentro, Peter Van Loo, Charles Swanton, and TRACERx Consortium. "Abstract 1211: Allele-specific copy-number based deconvolution of bulk tumour RNA sequencing data from the TRACERx study." Cancer Research 82, no. 12_Supplement (June 15, 2022): 1211. http://dx.doi.org/10.1158/1538-7445.am2022-1211.
Повний текст джерелаAbuhusain, Hazem, and Veejay Bagga. "Redefining a Rare CNS Tumour Through Targeted Genetic Sequencing." Neuro-Oncology 24, Supplement_4 (October 1, 2022): iv15—iv16. http://dx.doi.org/10.1093/neuonc/noac200.068.
Повний текст джерелаHanna, Tom, Nick Bryan, Damian Bond, John Hunt, Chris Stanley, Paula Ghaneh, and William Greenhalf. "Next generation sequencing of Tp53 in circulating tumour cells." Pancreatology 14, no. 3 (June 2014): S83—S84. http://dx.doi.org/10.1016/j.pan.2014.05.663.
Повний текст джерелаDavis, John, Matthew Petterson, James Newell, Gregory Y. Lauwers, Thomas Royce, and Michael J. Demeure. "Micrometastatic gastric glomus tumour confirmed by next-generation sequencing." Histopathology 72, no. 2 (October 24, 2017): 351–54. http://dx.doi.org/10.1111/his.13303.
Повний текст джерелаKuipers, Jack, Katharina Jahn, and Niko Beerenwinkel. "Advances in understanding tumour evolution through single-cell sequencing." Biochimica et Biophysica Acta (BBA) - Reviews on Cancer 1867, no. 2 (April 2017): 127–38. http://dx.doi.org/10.1016/j.bbcan.2017.02.001.
Повний текст джерелаde Sousa, Sílvia Ferreira, Marina Gonçalves Diniz, Josiane Alves França, Thaís dos Santos Fontes Pereira, Rennan Garcias Moreira, Jean Nunes dos Santos, Ricardo Santiago Gomez, and Carolina Cavalieri Gomes. "Cancer genes mutation profiling in calcifying epithelial odontogenic tumour." Journal of Clinical Pathology 71, no. 3 (November 10, 2017): 279–83. http://dx.doi.org/10.1136/jclinpath-2017-204813.
Повний текст джерелаMacgeoch, Catriona, Diana M. Barnes, Julia A. Newton, Shehla Mohammed, Shirley V. Hodgson, Mun Ng, D. Timothy Bishop, and Nigel K. Spurr. "p53 Protein Detected By Immunohistochemical Staining is Not Always Mutant." Disease Markers 11, no. 5-6 (1993): 239–50. http://dx.doi.org/10.1155/1993/480686.
Повний текст джерелаBurghel, George J., Carolyn D. Hurst, Christopher M. Watson, Phillip A. Chambers, Helen Dickinson, Paul Roberts, and Margaret A. Knowles. "Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms." BioMed Research International 2015 (2015): 1–6. http://dx.doi.org/10.1155/2015/478017.
Повний текст джерелаTaylor, William S., John Pearson, Allison Miller, Sebastian Schmeier, Frank A. Frizelle, and Rachel V. Purcell. "MinION Sequencing of colorectal cancer tumour microbiomes—A comparison with amplicon-based and RNA-Sequencing." PLOS ONE 15, no. 5 (May 20, 2020): e0233170. http://dx.doi.org/10.1371/journal.pone.0233170.
Повний текст джерелаMoore, Ariane L., Aashil A. Batavia, Jack Kuipers, Jochen Singer, Elodie Burcklen, Peter Schraml, Christian Beisel, Holger Moch, and Niko Beerenwinkel. "Spatial Distribution of Private Gene Mutations in Clear Cell Renal Cell Carcinoma." Cancers 13, no. 9 (April 30, 2021): 2163. http://dx.doi.org/10.3390/cancers13092163.
Повний текст джерелаMoorcraft, Sing Yu, David Gonzalez de Castro, David Cunningham, Brian A. Walker, Sanna Hulkki Wilson, Javier Diez Perez, Clare Peckitt, et al. "FOrMAT: Feasibility of a molecular characterization approach to treatment of patients (pts) with advanced gastrointestinal (GI) tumors." Journal of Clinical Oncology 33, no. 3_suppl (January 20, 2015): TPS227. http://dx.doi.org/10.1200/jco.2015.33.3_suppl.tps227.
Повний текст джерелаWinter, Helen, P. Kaisaki, Rebecca Carter, Anthony Cutts, Tessa Greenhalgh, Anna Schuh, Ricky A. Sharma, and Jenny C. Taylor. "Sequencing cell free DNA in patients receiving selective internal radiation therapy for colorectal liver metastases." Journal of Clinical Oncology 35, no. 4_suppl (February 1, 2017): 646. http://dx.doi.org/10.1200/jco.2017.35.4_suppl.646.
Повний текст джерелаLoddo, Marco, Keeda-Marie Hardisty, Alexander Llewelyn, Tiffany Haddow, Robert Thatcher, and Gareth Williams. "Utilisation of semiconductor sequencing for detection of actionable fusions in solid tumours." PLOS ONE 17, no. 8 (August 19, 2022): e0246778. http://dx.doi.org/10.1371/journal.pone.0246778.
Повний текст джерелаWang, Pin, Yunshan Wang, Sasha A. Langley, Yan-Xia Zhou, Kuang-Yu Jen, Qi Sun, Colin Brislawn, et al. "Diverse tumour susceptibility in Collaborative Cross mice: identification of a new mouse model for human gastric tumourigenesis." Gut 68, no. 11 (March 6, 2019): 1942–52. http://dx.doi.org/10.1136/gutjnl-2018-316691.
Повний текст джерелаPan, Xiuyi, Mengni Zhang, Jin Yao, Hao Zeng, Ling Nie, Jing Gong, Xueqin Chen, Miao Xu, Qiao Zhou, and Ni Chen. "Fumaratehydratase-deficient renal cell carcinoma: a clinicopathological and molecular study of 13 cases." Journal of Clinical Pathology 72, no. 11 (July 1, 2019): 748–54. http://dx.doi.org/10.1136/jclinpath-2019-205924.
Повний текст джерелаChen, Hsin-Pai, Jeng-Kai Jiang, Chia-Hao Chan, Wan-Huai Teo, Chih-Yung Yang, Yen-Chung Chen, Teh-Ying Chou, Chi-Hung Lin, and Yu-Jiun Chan. "Genetic polymorphisms of the human cytomegalovirus UL144 gene in colorectal cancer and its association with clinical outcome." Journal of General Virology 96, no. 12 (December 1, 2015): 3613–23. http://dx.doi.org/10.1099/jgv.0.000308.
Повний текст джерелаHuang, Dachuan, Wan Lu Pang, Daryl Ming Zhe Cheah, Yurike Laurensia, Jing Quan Lim, Soo Yong Tan, Tiffany Tang, Soon Thye Lim, and Choon Kiat Ong. "A Patient Derived Xenograft As a Preclinical Model for Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma." Blood 132, Supplement 1 (November 29, 2018): 2949. http://dx.doi.org/10.1182/blood-2018-99-110899.
Повний текст джерелаZhang, Qi, Yu Lou, Jiaqi Yang, Junli Wang, Jie Feng, Yali Zhao, Lin Wang, et al. "Integrated multiomic analysis reveals comprehensive tumour heterogeneity and novel immunophenotypic classification in hepatocellular carcinomas." Gut 68, no. 11 (June 21, 2019): 2019–31. http://dx.doi.org/10.1136/gutjnl-2019-318912.
Повний текст джерелаGullapalli, Veena, Hannah Hsu, Vanita Bhargava, and Peter Presgrave. "Synchronous Development of Acute Megakaryoblastic Leukaemia and Disseminated Melanoma following Treatment of a Germ Cell Tumour: A Case Report." Case Reports in Oncology 14, no. 3 (November 17, 2021): 1638–44. http://dx.doi.org/10.1159/000519663.
Повний текст джерелаOoi, Wen Fong, Amrita M. Nargund, Kevin Junliang Lim, Shenli Zhang, Manjie Xing, Amit Mandoli, Jing Quan Lim, et al. "Integrated paired-end enhancer profiling and whole-genome sequencing reveals recurrent CCNE1 and IGF2 enhancer hijacking in primary gastric adenocarcinoma." Gut 69, no. 6 (September 21, 2019): 1039–52. http://dx.doi.org/10.1136/gutjnl-2018-317612.
Повний текст джерелаŚlaska, Brygida, Magdalena Surdyka, Adam Brodzki, Sylwia Nisztuk, Artur Gurgul, Monika Bugno-Poniewierska, Anna Śmiech, Dorota Różańska, and Maciej Orzelski. "Mitochondrial D-loop mutations can be detected in sporadic malignant tumours in dogs." Bulletin of the Veterinary Institute in Pulawy 58, no. 4 (December 1, 2014): 631–37. http://dx.doi.org/10.2478/bvip-2014-0096.
Повний текст джерелаO'Byrne, Kenneth John, Joanna Kapeleris, Arutha Kulasinghe, Majid E. Warkiani, Connor Gerard O'Leary, Rahul Ladwa, Ian Vela, Paul Leo, Peter Sternes, and Chamindie Punyadeera. "Culture of circulating tumour cells derived from non-small cell lung cancer." Journal of Clinical Oncology 38, no. 15_suppl (May 20, 2020): e21692-e21692. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e21692.
Повний текст джерелаLi, Rong, Shuangxiu Wu, Yuanyuan Chang, Yin Wang, and Boyi Li. "Whole-exome sequencing on circulating tumor cells explores platinum-based chemotherapy resistance in advanced non-small cell lung cancer." Journal of Clinical Oncology 39, no. 15_suppl (May 20, 2021): e21021-e21021. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e21021.
Повний текст джерелаMa, E. S. K., C. L. P. Wong, F. B. F. Law, W.-K. Chan, and D. Siu. "Detection of KRAS mutations in colorectal cancer by high-resolution melting analysis." Journal of Clinical Pathology 62, no. 10 (September 25, 2009): 886–91. http://dx.doi.org/10.1136/jcp.2008.063677.
Повний текст джерелаHiley, Crispin T., Kevin Litchfield, Oriol Pich, David Moore, Cristina Naceur-Lombardelli, Selvaraju Veeriah, Maise Al Bakir, et al. "Abstract 645: Heterogeneity of immunotherapy biomarkers in the TRACERx non-small cell lung cancer multi-region lung cancer cohort study." Cancer Research 82, no. 12_Supplement (June 15, 2022): 645. http://dx.doi.org/10.1158/1538-7445.am2022-645.
Повний текст джерелаLeBlanc, VG, D. Trinh, M. Hughes, I. Luthra, D. Livingstone, MD Blough, JG Cairncross, JJ Kelly, and MA Marra. "1450-1545 Young Investigator Awards & Presentations Basic/Translational Exploring cellular subpopulations in glioblastoma and matched organoids using single-cell RNA-seq 52." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, S3 (June 2018): S13—S14. http://dx.doi.org/10.1017/cjn.2018.297.
Повний текст джерелаCaushi, Justina X., Jiajia Zhang, Zhicheng Ji, Ajay Vaghasia, Boyang Zhang, Emily Han-Chung Hsiue, Brian J. Mog, et al. "Transcriptional programs of neoantigen-specific TIL in anti-PD-1-treated lung cancers." Nature 596, no. 7870 (July 21, 2021): 126–32. http://dx.doi.org/10.1038/s41586-021-03752-4.
Повний текст джерелаGhorani, Ehsan, James L. Reading, Jake Y. Henry, Marc Robert De Massy, Rachel Rosenthal, Andrew J. S. Furness, Assma Ben Aissa, et al. "Association of the imbalance between early and late differentiated intra-tumor CD4 T cells with mutational burden in non-small cell lung cancer." Journal of Clinical Oncology 37, no. 15_suppl (May 20, 2019): 2590. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.2590.
Повний текст джерелаCrisafulli, Giovanni, Benedetta Mussolin, Andrea Cassingena, Monica Montone, Alice Bartolini, Ludovic Barault, Antonia Martinetti, et al. "Whole exome sequencing analysis of urine trans-renal tumour DNA in metastatic colorectal cancer patients." ESMO Open 4, no. 6 (November 2019): e000572. http://dx.doi.org/10.1136/esmoopen-2019-000572.
Повний текст джерелаYaegashi, Mizunori, Takeshi Iwaya, Noriyuki Sasaki, Masashi Fujita, Zhenlin Ju, Doris Siwak, Tsuyoshi Hachiya, et al. "Frequent post-operative monitoring of colorectal cancer using individualised ctDNA validated by multiregional molecular profiling." British Journal of Cancer 124, no. 9 (March 3, 2021): 1556–65. http://dx.doi.org/10.1038/s41416-021-01266-4.
Повний текст джерелаAsmann, Y., K. Parikh, M. Borad, L. Bergsagel, and A. S. Mansfield. "84MO Tumour-only sequencing led to inflated tumour mutational burden estimation especially in under-represented ethnic groups." Annals of Oncology 31 (September 2020): S274—S275. http://dx.doi.org/10.1016/j.annonc.2020.08.205.
Повний текст джерелаCheng, Michael L., Michael F. Berger, David M. Hyman, and David B. Solit. "Clinical tumour sequencing for precision oncology: time for a universal strategy." Nature Reviews Cancer 18, no. 9 (July 20, 2018): 527–28. http://dx.doi.org/10.1038/s41568-018-0043-2.
Повний текст джерелаYadav, Mahesh, Suchit Jhunjhunwala, Qui T. Phung, Patrick Lupardus, Joshua Tanguay, Stephanie Bumbaca, Christian Franci, et al. "Predicting immunogenic tumour mutations by combining mass spectrometry and exome sequencing." Nature 515, no. 7528 (November 26, 2014): 572–76. http://dx.doi.org/10.1038/nature14001.
Повний текст джерелаMahamdallie, Shazia, Shawn Yost, Emma Poyastro-Pearson, Esty Holt, Anna Zachariou, Sheila Seal, Anna Elliott, et al. "Identification of new Wilms tumour predisposition genes: an exome sequencing study." Lancet Child & Adolescent Health 3, no. 5 (May 2019): 322–31. http://dx.doi.org/10.1016/s2352-4642(19)30018-5.
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