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Mostrando 581 - 600 Resultados de 9,396 Para Buscar '"Sanger"', tiempo de consulta: 0.61s Limitar resultados
  1. 581
    “…We have shown that rs396991 can be genotyped by PCR amplification, followed by direct Sanger sequencing of the product, without coamplification of FCGR3B, and that the rs396991 TaqMan assay (C__25815666_10) agrees with Sanger sequencing results in 100% of European and Asian samples tested, but it has a small error rate in African and American populations. …”
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    Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method
  2. 582
    “…This pool was obtained in a classical SELEX (Systematic Evolution of Ligands by EXponential enrichment) experiment using the FluMag-SELEX procedure followed by cloning and Sanger sequencing. PA#2/8 was identified as the only Protein A-binding aptamer from the Sanger sequence pool, and was shown to be able to bind intact cells of Staphylococcus aureus. …”
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    Refining the Results of a Classical SELEX Experiment by Expanding the Sequence Data Set of an Aptamer Pool Selected for Protein A
  3. 583
    “…NGS was compared to traditional PCR and direct Sanger sequencing for its ability to detect Giardia species, assemblages, and mixed assemblage infections. …”
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    Assessment of next generation amplicon sequencing of the beta-giardin gene for the detection of Giardia duodenalis assemblages and mixed infections
  4. 584
    por Miao, Yue, Tang, Siyuan
    Publicado 2022
    “…Meanwhile, multiplex polymerase chain reaction (mPCR) and mPCR-next-generation sequencing (mPCR-NGS) were used to detect BRCA1/2 genome. Sanger test was used for newly high virulent mutations to verify the correctness of mutagenic sites. …”
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    Detection of Breast Cancer Lump and BRCA1/2 Genetic Mutation under Deep Learning
  5. 585
    “…Availability: The executable and user manual can be freely downloaded from ftp://ftp.sanger.ac.uk/pub/zn1/HI. Contact: ql2@sanger.ac.uk…”
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    HI: haplotype improver using paired-end short reads
  6. 586
    “…The results were compared to culture results, if available, and to the results of Sanger sequencing of the 16S rRNA gene (16S Sanger sequencing). …”
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    Targeting the 16S rRNA Gene by Reverse Complement PCR Next-Generation Sequencing: Specific and Sensitive Detection and Identification of Microbes Directly in Clinical Samples
  7. 587
    “…Conclusion: Overall, conventional Sanger sequencing and next-generation-sequencing-based clonality and somatic hypermutation analyses gave comparable results. …”
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    Single-Step IGHV Next-Generation Sequencing Detects Clonality and Somatic Hypermutation in Lymphoid Malignancies: A Phase III Diagnostic Accuracy Study
  8. 588
    “…Furthermore, all the newly detected mutations in patients from the training set have been confirmed by Sanger sequencing. Absence of any false negative event has been excluded by testing some of the negative patients, randomly selected, with Sanger sequencing. …”
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    Diagnosis of Noonan syndrome and related disorders using target next generation sequencing
  9. 589
    “…Compared with Sanger sequencing, the total sensitivity and specificity of NGS assays was 95.24% (40/42) and 77.14% (54/70), respectively. …”
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    Next-generation sequencing-based detection of EGFR, KRAS, BRAF, NRAS, PIK3CA, Her-2 and TP53 mutations in patients with non-small cell lung cancer
  10. 590
    “…Next, we performed a pilot with both Sanger sequencing and MinION based sequencing of 14 DNA samples which showed a good concordance between Sanger- and MinION sequencing. …”
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    A comprehensive overview of FCGR3A gene variability by full-length gene sequencing including the identification of V158F polymorphism
  11. 591
    “…MLPA results with single exon deletions were validated with PCR amplification and Sanger sequencing. The negative results of MLPA were further analysed with NGS and validated by Sanger sequencing. …”
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    Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy
  12. 592
    “…Next-generation sequencing (NGS) provides the possibility to detect drug resistance mutations with higher sensitivity than Sanger sequencing. The aim of this study was to search for transmitted drug resistance (TDR) mutations in strains from PWID recently diagnosed with HIV infection by parallel use of Sanger sequencing and NGS. …”
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    A16 Next-generation sequencing to detect transmitted drug resistance mutations in Romanian people who inject drugs
  13. 593
    “…PURPOSE: Next-generation sequencing (NGS) is rapidly replacing Sanger sequencing in genetic diagnostics. Sensitivity and specificity of NGS approaches are not well-defined, but can be estimated from applying NGS and Sanger sequencing in parallel. …”
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    Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population
  14. 594
    “…METHODS: Five cases of confirmed intra-amniotic infection, determined by either cultivation or 16S rDNA polymerase chain reaction (PCR) Sanger sequencing, and 10 cases of women who underwent mid-trimester genetic amniocentesis were included. …”
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    Rapid diagnosis of intra-amniotic infection using nanopore-based sequencing
  15. 595
    por Ullah, Asmat, Syed, Fibhaa, Khan, Shazia
    Publicado 2023
    “…Genetic investigation was done by performing whole exome sequencing (WES) using DNA of the patients. Sanger sequencing was performed to validate WES findings and segregation analysis in the family. …”
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    c.151dup variant in LAMA3 in Pakistani patients affected with Shabbir Syndrome but showing mild symptoms
  16. 596
    “…We developed metagenomic read simulators with platform-specific (Sanger, pyrosequencing, Illumina) base-error models, and simulated metagenomes of differing community complexities. …”
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    Assessment of Metagenomic Assembly Using Simulated Next Generation Sequencing Data
  17. 597
    “…All were analyzed by ASLNAqPCR and Sanger sequencing. Discordant cases were pyrosequenced. …”
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    Allele Specific Locked Nucleic Acid Quantitative PCR (ASLNAqPCR): An Accurate and Cost-Effective Assay to Diagnose and Quantify KRAS and BRAF Mutation
  18. 598
    “…BACKGROUND: The STINGRAY system has been conceived to ease the tasks of integrating, analyzing, annotating and presenting genomic and expression data from Sanger and Next Generation Sequencing (NGS) platforms. …”
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    STINGRAY: system for integrated genomic resources and analysis
  19. 599
    “…To identify genes important in skin development and homeostasis, we have applied a high throughput, multi-parameter phenotype screen to the conditional targeted mutant mice generated by the Wellcome Trust Sanger Institute's Mouse Genetics Project (Sanger-MGP). …”
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    Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse
  20. 600
    “…Our study validates the use of targeted OS-Seq for genetic diagnostics of PAH and revealed pathogenic variants that had been previously missed using Sanger sequencing.…”
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    Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing
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