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5. The utility of next-generation sequencing in diagnosis and monitoring of acute myeloid leukemia and myelodysplastic syndromes. Duncavage EJ; Tandon B Int J Lab Hematol; 2015 May; 37 Suppl 1():115-21. PubMed ID: 25976969 [TBL] [Abstract][Full Text] [Related]
6. [Using next generation sequencing technology to analyze gene mutations in patients with acute myeloid leukemia and the impact on prognosis]. Zhao CX; Wang JM; Li JM; Zou SH; Chen FY; Liang AB; Hou J; Hu XX; Zhang YX; Gu SY; Zhu JY; Li P; Du J; Yang YN; Qin YW; Wang XR; Wang C Zhonghua Yi Xue Za Zhi; 2019 Oct; 99(40):3145-3151. PubMed ID: 31694105 [No Abstract] [Full Text] [Related]
7. Archived bone marrow smears are an excellent source for NGS-based mutation detection in acute myeloid leukemia. Al Hinai ASA; Grob T; Kavelaars FG; Rijken M; Zeilemaker A; Erpelinck-Verschueren CAJ; Gussinklo KJ; Sanders MA; van Lom K; Valk PJM Leukemia; 2020 Aug; 34(8):2220-2224. PubMed ID: 32060404 [No Abstract] [Full Text] [Related]
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12. Centrifuged supernatants from FNA provide a liquid biopsy option for clinical next-generation sequencing of thyroid nodules. Ye W; Hannigan B; Zalles S; Mehrotra M; Barkoh BA; Williams MD; Cabanillas ME; Edeiken-Monroe B; Hu P; Duose D; Wistuba II; Medeiros LJ; Stewart J; Luthra R; Roy-Chowdhuri S Cancer Cytopathol; 2019 Mar; 127(3):146-160. PubMed ID: 30620446 [TBL] [Abstract][Full Text] [Related]
13. Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer. Janku F; Zhang S; Waters J; Liu L; Huang HJ; Subbiah V; Hong DS; Karp DD; Fu S; Cai X; Ramzanali NM; Madwani K; Cabrilo G; Andrews DL; Zhao Y; Javle M; Kopetz ES; Luthra R; Kim HJ; Gnerre S; Satya RV; Chuang HY; Kruglyak KM; Toung J; Zhao C; Shen R; Heymach JV; Meric-Bernstam F; Mills GB; Fan JB; Salathia NS Clin Cancer Res; 2017 Sep; 23(18):5648-5656. PubMed ID: 28536309 [No Abstract] [Full Text] [Related]
14. Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing. Mu W; Lu HM; Chen J; Li S; Elliott AM J Mol Diagn; 2016 Nov; 18(6):923-932. PubMed ID: 27720647 [TBL] [Abstract][Full Text] [Related]
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17. Evaluation of copy number variant detection from panel-based next-generation sequencing data. Yao R; Yu T; Qing Y; Wang J; Shen Y Mol Genet Genomic Med; 2019 Jan; 7(1):e00513. PubMed ID: 30565893 [TBL] [Abstract][Full Text] [Related]
18. Targeted next-generation sequencing of circulating cell-free DNA vs bone marrow in patients with acute myeloid leukemia. Short NJ; Patel KP; Albitar M; Franquiz M; Luthra R; Kanagal-Shamanna R; Wang F; Assi R; Montalban-Bravo G; Matthews J; Ma W; Loghavi S; Takahashi K; Issa GC; Kornblau SM; Jabbour E; Garcia-Manero G; Kantarjian HM; Estrov Z; Ravandi F Blood Adv; 2020 Apr; 4(8):1670-1677. PubMed ID: 32324887 [TBL] [Abstract][Full Text] [Related]
19. Variant allele frequencies do not correlate well with myeloblast counts in a clinically validated gene sequencing panel for routine acute myeloid leukemia workup. Toth LN; Green D; Peterson J; Deharvengt SJ; de Abreu FB; Loo EY Leuk Lymphoma; 2019 Oct; 60(10):2415-2422. PubMed ID: 30997856 [TBL] [Abstract][Full Text] [Related]
20. Assessment of the clinical utility of four NGS panels in myeloid malignancies. Suggestions for NGS panel choice or design. Aguilera-Diaz A; Vazquez I; Ariceta B; Mañú A; Blasco-Iturri Z; Palomino-Echeverría S; Larrayoz MJ; García-Sanz R; Prieto-Conde MI; Del Carmen Chillón M; Alfonso-Pierola A; Prosper F; Fernandez-Mercado M; Calasanz MJ PLoS One; 2020; 15(1):e0227986. PubMed ID: 31978184 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]