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Mostrando 1 - 20 Resultados de 9,396 Para Buscar '"Sanger"', tiempo de consulta: 0.22s Limitar resultados
  1. 1
    “…AVAILABILITY AND IMPLEMENTATION: SangeR is freely available at https://github.com/Neuropathology-Giessen/SangeR and https://hub.docker.com/repository/docker/kaischmid/sange_r CONTACT: Kai.Schmid@patho.med.uni-giessen.de or Daniel.Amsel@patho.med.uni-giessen.de SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.…”
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    SangeR: the high-throughput Sanger sequencing analysis pipeline
  2. 2
    “…We propose a novel method, which we called qSanger, to quantify DNA using amplitude ratios of aligned electropherogram peaks from mixed Sanger sequencing reads. …”
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    qSanger: Quantification of Genetic Variants in Bacterial Cultures by Sanger Sequencing
  3. 3
    Publicado 1911
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    Robert M. Sanger
  4. 4
    Publicado 1903
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    Professor Max Sänger
  5. 5
    Publicado 1886
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    Sänger’s Cæsarean Operation
  6. 6
    Publicado 1978
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    Pioneer of the future: Margaret Sanger
  7. 7
    por Roe, Bruce A.
    Publicado 2014
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    Frederick Sanger (1918–2013)
  8. 8
    por Dooley, Erin E.
    Publicado 2006
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    EHPnet: Wellcome Trust Sanger Institute
  9. 9
    por Fields, Stanley
    Publicado 2014
    “…Fred Sanger developed technologies that won him two Nobel Prizes and revolutionized biological research. …”
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    Would Fred Sanger Get Funded Today?
  10. 10
    “…Investigators from the EuroEPINOMICS rare epilepsy syndromes Dravet working group performed whole-exome sequencing on 31 trios that had been reported negative for SCN1A mutations by Sanger sequencing.…”
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    Genetic Testing Requires NGS and Sanger Methodologies
  11. 11
    “…BACKGROUND: Although high-throughput sequencers (HTS) have largely displaced their Sanger counterparts, the short read lengths and high error rates of most platforms constrain their utility for amplicon sequencing. …”
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    A Sequel to Sanger: amplicon sequencing that scales
  12. 12
    “…Merging Sanger sequences is frequently needed during the gene cloning process. …”
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    A Python script to merge Sanger sequences
  13. 13
    por Vernon, Matthew
    Publicado 2019
    “…--HTML-->The Wellcome Sanger Institute has 18PB in its largest Ceph cluster. …”
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    Ceph Supporting Genetic Research at The Wellcome Sanger Institute
  14. 14
    por Seroussi, Eyal
    Publicado 2021
    “…Indeed, recent developments in software tools (e.g., TIDE, ICE, EditR, BEEP and BEAT) indicate that quantification based on direct Sanger sequencing is gaining in scientific acceptance. …”
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    Estimating Copy-Number Proportions: The Comeback of Sanger Sequencing
  15. 15
    “…Heteroplasmy can be detected by visual inspection of Sanger sequencing chromatograms, where it appears as multiple peaks of fluorescence at a single nucleotide position. …”
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    PHFinder: assisted detection of point heteroplasmy in Sanger sequencing chromatograms
  16. 16
    “…A hybrid assembly of both Sanger- and pyrosequencing-derived ESTs resulted in 34,495 unique sequences with 1,110 sequences (3.2%) that were solely derived from Sanger sequencing alone. …”
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    Analysis of the Pythium ultimum transcriptome using Sanger and Pyrosequencing approaches
  17. 17
    “…Here, we present CRISP-ID, a web application which uses a unique algorithm for genotyping up to three alleles from a single Sanger sequencing trace, providing a robust and readily accessible platform to directly identify indels and significantly speed up the characterization of clones.…”
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    CRISP-ID: decoding CRISPR mediated indels by Sanger sequencing
  18. 18
    por Jin, Jie-Qiong, Sun, Yan-Bo
    Publicado 2018
    “…With the wide application of DNA sequencing technology, DNA sequences are increasingly generated through the Sanger sequencing platform. SeqMan (in the LaserGene package) is an excellent program with an easy-to-use graphical user interface (GUI) employed to assemble Sanger sequences into contigs. …”
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    AutoSeqMan: batch assembly of contigs for Sanger sequences
  19. 19
    por Sanger, Keith, 1948-
    Publicado 1998
    Libro
    The language of fiction /
  20. 20
    por Holland, Dave
    Publicado 2019
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    Wellcome Sanger Institute - Supporting DNA Sequencing at Scale with OpenStack
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