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Mostrando 501 - 520 Resultados de 9,396 Para Buscar '"Sanger"', tiempo de consulta: 0.19s Limitar resultados
  1. 501
    “…Patients were investigated for TP53 mutation by Sanger and by MinION sequencing. Analysis by Sanger was performed according with the IARC protocol. …”
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    TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing
  2. 502
    “…In 47 cases, MB could be performed: Sanger sequencing and ASQ‐PCR in 34 cases, ASQ‐PCR only in 11 cases, and Sanger sequencing only in two cases. …”
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    BRAF‐V600E immunohistochemistry in a large series of glial and glial–neuronal tumors
  3. 503
    “…NGS detected all true high-frequency drug resistance mutations (>20% frequency) found by Sanger sequencing, with greater accuracy in one instance of a Sanger-detected false positive. …”
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    Limited Marginal Utility of Deep Sequencing for HIV Drug Resistance Testing in the Age of Integrase Inhibitors
  4. 504
    “…Comparison between dPCR and Sanger sequencing showed a sensitivity of 100% (95% CI 53–100%), and a specificity of 84.2% (95% CI 83–84.2%). …”
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    Chip-based digital Polymerase Chain Reaction as quantitative technique for the detection of PIK3CA mutations in breast cancer patients
  5. 505
    “…Massively parallel sequencing (MPS) technologies, such as 454-pyrosequencing, allow for the identification of variants in sequence populations at lower levels than consensus sequencing and most single-template Sanger sequencing experiments. We sought to determine if the greater depth of population sampling attainable using MPS technology would allow detection of minor variants in HIV founder virus populations very early in infection in instances where Sanger sequencing detects only a single variant. …”
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    Comparison of Major and Minor Viral SNPs Identified through Single Template Sequencing and Pyrosequencing in Acute HIV-1 Infection
  6. 506
    Publicado 2018
    “…As for consistency test, the Kappa values of assay panels with Sanger sequencing, assay panels with ARMS-PCR, and ARMS-PCR with Sanger sequencing were 0.946, 0.953, and 0.913, respectively. …”
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    AMSS-PCR在肺癌突变基因检测中的价值研究
  7. 507
    “…The Idylla™ real-time (RT)-PCR is compared to the routine method used in our laboratory, which combines next generation and Sanger sequencing, for the detection of EGFR mutations in LCBM. …”
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    Rapid detection of EGFR mutations in decalcified lung cancer bone metastasis
  8. 508
    por Ali Khan, Imran
    Publicado 2021
    “…Genetic analysis was previously performed using first-generation sequencing techniques, such as DNA-Sanger sequencing, which uses chain-terminating inhibitors. …”
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    Do second generation sequencing techniques identify documented genetic markers for neonatal diabetes mellitus?
  9. 509
    “…We also assessed whether cNGS or Sanger sequencing-identified mutations have an association with clinical outcomes in uPA. …”
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    Novel Mutations Detection with Next-Generation Sequencing and Its Association with Clinical Outcome in Unilateral Primary Aldosteronism
  10. 510
    “…Currently, for a salmonid reference sequence, it appears that a substantial portion of sequencing should be done using Sanger technology.…”
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    Assessing the feasibility of GS FLX Pyrosequencing for sequencing the Atlantic salmon genome
  11. 511
    “…We report the design of a targeted resequencing panel for monogenic dyslipidemias, LipidSeq, for the purpose of replacing Sanger sequencing in the clinical detection of dyslipidemia-causing variants. …”
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    LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias
  12. 512
    “…Such mismatches may be solved by Massively Parallel Sequencing (MPS), allowing more sensitive quantitative analysis for mixed positions than Sanger. The mtDNA control region was analysed in buccal reference samples from 26 individuals and 475 corresponding hairs by MPS and compared to Sanger sequencing data generated on the same samples. …”
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    Reducing the Number of Mismatches between Hairs and Buccal References When Analysing mtDNA Heteroplasmic Variation by Massively Parallel Sequencing
  13. 513
    “…Greater numbers of species were detected by pyrosequencing than by Sanger sequencing. Rare taxa constituted nearly 6% of each pyrotag community and less than 1% of the Sanger sequencing community. …”
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    Target Region Selection Is a Critical Determinant of Community Fingerprints Generated by 16S Pyrosequencing
  14. 514
    “…RESULTS: Among 44 patients recruited, 14 DRM were detected by Sanger in 12 patients (27%) and 20 DRM were detected by NGS, in 16 (36%). …”
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    Improvement in detecting cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance using next generation sequencing
  15. 515
    “…In a validation study, all 17 resistance mutations found by Sanger sequencing were also detected by long-read sequencing. …”
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    Migrating to Long-Read Sequencing for Clinical Routine BCR-ABL1 TKI Resistance Mutation Screening
  16. 516
    “…SIMPLE SUMMARY: In this study, the high oncogenic mutation frequency (96%) of small GISTs is identified by whole-exome sequencing and targeted sanger sequencing in the entire cohort (n = 76) of a Chinese population. …”
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    Small Gastric Stromal Tumors: An Underestimated Risk
  17. 517
    “…Traditionally, spa typing is performed by Sanger sequencing but has in recent years been replaced by whole-genome sequencing (WGS) in some laboratories. …”
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    spa Typing of Methicillin-Resistant Staphylococcus aureus Based on Whole-Genome Sequencing: the Impact of the Assembler
  18. 518
    por Schumann, Robert, 1810-1856
    Publicado 1981
    Tabla de Contenidos:
    Partituras Libro
    Selected songs : for solo voice and piano
  19. 519
    “…No transmitted resistance to integrase inhibitors was found in our population by Sanger sequencing or UDS.…”
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    Analysis of transmitted HIV-1 drug resistance using 454 ultra-deep-sequencing and the DeepChek(®)-HIV system
  20. 520
    “…The congenital muscular dystrophies (CMDs) comprise a heterogeneous group of heritable muscle disorders with often difficult to interpret muscle pathology, making them challenging to diagnose. Serial Sanger sequencing of suspected CMD genes, while the current molecular diagnostic method of choice, can be slow and expensive. …”
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    Comprehensive Mutation Analysis for Congenital Muscular Dystrophy: A Clinical PCR-Based Enrichment and Next-Generation Sequencing Panel
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