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Mostrando 41 - 60 Resultados de 9,396 Para Buscar '"Sanger"', tiempo de consulta: 0.37s Limitar resultados
  1. 41
    por Brand, Richard A.
    Publicado 2008
    “…This biographical sketch of Eugene F. Sanger, AM, MD, corresponds to the historic text, The Classic: Report of the Committee on Suits for Malpractice, available at DOI 10.1007/s11999-008-0639-z.…”
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    Clinical Risk and Judicial Reasoning: Eugene F. Sanger, AM, MD, 1829–1897
  2. 42
    “…This article defines the FASTQ format, covering the original Sanger standard, the Solexa/Illumina variants and conversion between them, based on publicly available information such as the MAQ documentation and conventions recently agreed by the Open Bioinformatics Foundation projects Biopython, BioPerl, BioRuby, BioJava and EMBOSS. …”
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    The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants
  3. 43
    “…However, at present, taxonomic binning tools for metagenomes discard 30-40% of Sanger sequencing data due to the stringency of BLAST cut-offs. …”
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    Reanalyze unassigned reads in Sanger based metagenomic data using conserved gene adjacency
  4. 44
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    Medium-sized deletion in the BRCA1 gene: Limitations of Sanger sequencing and MLPA analyses
  5. 45
    “…Conventional Sanger sequencing remains time-consuming and laborious. …”
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    Online Artículo Texto
    Rapid Sanger Sequencing of the 16S rRNA Gene for Identification of Some Common Pathogens
  6. 46
    “…The reference assembly for the domestic horse, EquCab2, published in 2009, was built using approximately 30 million Sanger reads from a Thoroughbred mare named Twilight. …”
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    Comparison of the Equine Reference Sequence with Its Sanger Source Data and New Illumina Reads
  7. 47
    “…Confirmatory Sanger sequencing supported the original Sanger report for three of the five discordant bases, one was shown to be a false positive supporting the WES data, and one result differed from both the Sanger and WES data. …”
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    Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care
  8. 48
    “…In 1977, Frederick Sanger developed a new method for DNA sequencing based on the chain termination method, now known as the Sanger sequencing method (SSM).  …”
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    Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome
  9. 49
    “…Among the 100 negative cases, three were positive for a rare EGFR mutation by Sanger sequencing. In the curative effect analysis of EGFR-TKIs, the progression-free survival (PFS) analysis based on ARMS and Sanger sequencing results showed no difference. …”
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    Detection of Rare Mutations in EGFR-ARMS-PCR-Negative Lung Adenocarcinoma by Sanger Sequencing
  10. 50
    “…Sanger sequences were aligned and edited using RECall software (beta v3.03). …”
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    Sanger and Next Generation Sequencing Approaches to Evaluate HIV-1 Virus in Blood Compartments
  11. 51
    “…Here, we quantify amplicon composition in synthetic bacterial communities through Sanger sequencing. We PCR amplify a universal marker gene, then we sequence this amplicon mixture in a single Sanger sequencing reaction. …”
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    Rapid, Inexpensive Measurement of Synthetic Bacterial Community Composition by Sanger Sequencing of Amplicon Mixtures
  12. 52
    “…The genotyping was performed by Sanger sequencing, optimized to overcome GC content drawbacks. …”
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    APOE Variants in an Iberian Alzheimer Cohort Detected through an Optimized Sanger Sequencing Protocol
  13. 53
    “…NGSure utilizes Blocker Displacement Amplification to first enrich the allelic fraction of the mutation and then uses Sanger sequencing to determine mutation identity. …”
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    Confirming putative variants at ≤ 5% allele frequency using allele enrichment and Sanger sequencing
  14. 54
    “…MOTIVATION: Despite the advent of next-generation sequencing technology and its widespread applications, Sanger sequencing remains instrumental for molecular biology subcloning work in biological and medical research and indispensable for drug discovery campaigns. …”
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    TraceTrack, an open-source software for batch processing, alignment and visualization of sanger sequencing chromatograms
  15. 55
    “…Method: The results of Sanger sequencing of peripheral blood RNA without NMD inhibition performed on potential splicing variants of tumor suppressor genes were retrospectively reviewed. …”
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    Reclassification of variants of tumor suppressor genes based on Sanger RNA sequencing without NMD inhibition
  16. 56
    “…CONCLUSION: We compared performances of iAssembler and several other de novo EST assembly programs using both Roche-454 and Sanger EST datasets. It demonstrated that iAssembler generated significantly more accurate consensus sequences than other assembly programs.…”
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    iAssembler: a package for de novo assembly of Roche-454/Sanger transcriptome sequences
  17. 57
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    Comparing ion torrent with pyrosequencing and Sanger sequencing for the detection of TP53 mutations in colorectal cancer
  18. 58
    “…Definitive diagnosis of primary hyperoxaluria (PH) currently utilizes sequential Sanger sequencing of the AGXT, GRPHR, and HOGA1 genes but efficacy is unproven. …”
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    Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing
  19. 59
    “…A distinctive oral phenotype is shared in both conditions. On Sanger sequencing of FAM20A in cases with that phenotype, we identified two probands with single, likely pathogenic heterozygous mutations. …”
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    A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing
  20. 60
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    Comparison of Targeted Next-Generation and Sanger Sequencing for the BRCA1 and BRCA2 Mutation Screening
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