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Journal Abstract Search

406 related items for PubMed ID: 28826610

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  • 5. Ioncopy: an R Shiny app to call copy number alterations in targeted NGS data.
    Budczies J, Pfarr N, Romanovsky E, Endris V, Stenzinger A, Denkert C.
    BMC Bioinformatics; 2018 Apr 24; 19(1):157. PubMed ID: 29699497
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  • 7. Building a Robust Tumor Profiling Program: Synergy between Next-Generation Sequencing and Targeted Single-Gene Testing.
    Hiemenz MC, Kadauke S, Lieberman DB, Roth DB, Zhao J, Watt CD, Daber RD, Morrissette JJ.
    PLoS One; 2016 Apr 24; 11(4):e0152851. PubMed ID: 27043212
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  • 12. Targeted DNA methylation analysis by next-generation sequencing.
    Masser DR, Stanford DR, Freeman WM.
    J Vis Exp; 2015 Feb 24; (96):. PubMed ID: 25741966
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  • 13. Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data.
    Favero F, Joshi T, Marquard AM, Birkbak NJ, Krzystanek M, Li Q, Szallasi Z, Eklund AC.
    Ann Oncol; 2015 Jan 24; 26(1):64-70. PubMed ID: 25319062
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  • 14. A Targeted High-Throughput Next-Generation Sequencing Panel for Clinical Screening of Mutations, Gene Amplifications, and Fusions in Solid Tumors.
    Luthra R, Patel KP, Routbort MJ, Broaddus RR, Yau J, Simien C, Chen W, Hatfield DZ, Medeiros LJ, Singh RR.
    J Mol Diagn; 2017 Mar 24; 19(2):255-264. PubMed ID: 28017569
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  • 15. DNA Methylation Analysis by Bisulfite Conversion Coupled to Double Multiplexed Amplicon-Based Next-Generation Sequencing (NGS).
    Bashtrykov P, Jeltsch A.
    Methods Mol Biol; 2018 Mar 24; 1767():367-382. PubMed ID: 29524146
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  • 16. Single-Center Experience with a Targeted Next Generation Sequencing Assay for Assessment of Relevant Somatic Alterations in Solid Tumors.
    Paasinen-Sohns A, Koelzer VH, Frank A, Schafroth J, Gisler A, Sachs M, Graber A, Rothschild SI, Wicki A, Cathomas G, Mertz KD.
    Neoplasia; 2017 Mar 24; 19(3):196-206. PubMed ID: 28161563
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  • 17. Comprehensive Screening of Gene Copy Number Aberrations in Formalin-Fixed, Paraffin-Embedded Solid Tumors Using Molecular Inversion Probe-Based Single-Nucleotide Polymorphism Array.
    Singh RR, Mehrotra M, Chen H, Almohammedsalim AA, Sahin A, Bosamra A, Patel KP, Routbort MJ, Lu X, Ronald A, Mishra BM, Virani S, Medeiros LJ, Luthra R.
    J Mol Diagn; 2016 Sep 24; 18(5):676-687. PubMed ID: 27392636
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  • 18. SILO: A Computational Method for Detecting Copy Number Gain in Clinical Specimens Analyzed on a Next-Generation Sequencing Platform.
    Miller N, Bouma M, Sabatini L, Gulukota K.
    J Mol Diagn; 2021 Oct 24; 23(10):1241-1248. PubMed ID: 34365010
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  • 20. Addition of chromosomal microarray and next generation sequencing to FISH and classical cytogenetics enhances genomic profiling of myeloid malignancies.
    Mukherjee S, Sathanoori M, Ma Z, Andreatta M, Lennon PA, Wheeler SR, Prescott JL, Coldren C, Casey T, Rietz H, Fasig K, Woodford R, Hartley T, Spence D, Donnelan W, Berdeja J, Flinn I, Kozyr N, Bouzyk M, Correll M, Ho H, Kravtsov V, Tunnel D, Chandra P.
    Cancer Genet; 2017 Oct 24; 216-217():128-141. PubMed ID: 29025587
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