Materias dentro de su búsqueda.
Mostrando 521 - 540 Resultados de 9,396 Para Buscar '"Sanger"', tiempo de consulta: 0.45s Limitar resultados
  1. 521
    “…Availability and implementation: The WGE database is freely available at www.sanger.ac.uk/htgt/wge Contact: vvi@sanger.ac.uk or skarnes@sanger.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    WGE: a CRISPR database for genome engineering
  2. 522
    “…Availability: DNAPlotter is freely available (under a GPL licence) for download (for MacOSX, UNIX and Windows) at the Wellcome Trust Sanger Institute web sites: http://www.sanger.ac.uk/Software/Artemis/circular/ Contact: artemis@sanger.ac.uk…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Texto
    DNAPlotter: circular and linear interactive genome visualization
  3. 523
    “…Database URL: http://vega.sanger.ac.uk/index.html…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Community gene annotation in practice
  4. 524
    “…Sanger sequencing identified variant TPMT alleles including *3A (8, 3.2% of alleles), *3C (4, 1.6%), and *2 (1, 0.4%), and NUDT15 alleles including *2 (5, 3.6%) and *3 (1, 0.7%). …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Comparison of variants in TPMT and NUDT15 between sequencing and genotyping methods in a multistate pediatric institution
  5. 525
    “…MLPA analysis of BRCA1/2 in Sanger-negative patients revealed 2 LGRs. The LGRs accounted for 14.3% of all identified BRCA1 mutations, and the prevalence of LGRs identified in this study was 1.8% in 111 Sanger-negative patients. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    BRCA1/2 mutations, including large genomic rearrangements, among unselected ovarian cancer patients in Korea
  6. 526
    “…All mutations identified by BNA-clamp PCR with Sanger sequencing were also identified by next generation sequencing. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Accurate detection of KRAS, NRAS and BRAF mutations in metastatic colorectal cancers by bridged nucleic acid-clamp real-time PCR
  7. 527
    “…So, an appropriate mix of technologies may help resolve most difficulties, and eventually provide assemblies of high quality without requiring any Sanger-based input. RESULTS: We compared assemblies obtained using Sanger data with those from different inputs from New Sequencing Technologies. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Texto
    High quality draft sequences for prokaryotic genomes using a mix of new sequencing technologies
  8. 528
    “…By comparing these to >400 mtDNA substitution variants detected by Sanger, we found 98% concordance in variant detection. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Texto
    Mitochondrial DNA Variant Discovery and Evaluation in Human Cardiomyopathies through Next-Generation Sequencing
  9. 529
    “…Motivation: Large-scale phenotyping projects such as the Sanger Mouse Genetics project are ongoing efforts to help identify the influences of genes and their modification on phenotypes. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Using association rule mining to determine promising secondary phenotyping hypotheses
  10. 530
    “…Here, we compared Next Generation Sequencing (NGS) with De Novo assembly and Sanger sequencing for their ability to distinguish clonal and non-clonal amplicons after SGA on one plasma specimen. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification
  11. 531
    “…Segregation was performed by Sanger sequencing in her unaffected parents. In the father, the mosaicism of the variant was further analyzed by targeted NGS and droplet digital PCR (ddPCR) in the blood and by Sanger sequencing in other tissues. (3) Results: The NGS analysis revealed the novel germline heterozygous COL5A1 c.1369G>T, p.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Gonosomal Mosaicism for a Novel COL5A1 Pathogenic Variant in Classic Ehlers-Danlos Syndrome
  12. 532
    “…The dataset includes high-quality exome sequence data from 142 samples together with Sanger sequence data at 704 sites; 416 sites with variants and 288 sites at which variants were called by an NGS analysis tool, but no variant is present in the corresponding Sanger sequence. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis
  13. 533
    “…Phenotypic susceptibility testing (pDST) indicated PZA-R TB. Targeted Sanger sequencing reported wild-type PncA, indicating PZA-S TB. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Pyrazinamide-resistant Tuberculosis Obscured From Common Targeted Molecular Diagnostics
  14. 534
    “…Materials and Methods  Sanger sequencing was used to determine NUDT15 variants from 200 patients. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    A Simple, Rapid, and Cost-Effective PCR Procedure for Detection of NUDT15 Gene Variants in Vietnamese Patients with Acute Lymphoblastic Leukemia
  15. 535
    Publicado 2000
    “…Alan Coulson has two main roles at the Sanger Centre, revolving around the worm and the human genome projects. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Texto
    Nematode Functional Genomics
  16. 536
    “…Availability: Artemis and ACT are freely available (under a GPL licence) for download (for MacOSX, UNIX and Windows) at the Wellcome Trust Sanger Institute web sites: http://www.sanger.ac.uk/Software/Artemis/ http://www.sanger.ac.uk/Software/ACT/ Contact: artemis@sanger.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Texto
    Artemis and ACT: viewing, annotating and comparing sequences stored in a relational database
  17. 537
    “…The nine virus samples had a median of 12 PI resistance mutations by direct PCR Sanger sequencing. RESULTS: For each of the nine virus samples, deep sequencing showed that each of the individual viruses within a sample contained nearly all of the mutations detected by Sanger sequencing. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Collinearity of protease mutations in HIV-1 samples with high-level protease inhibitor class resistance
  18. 538
    “…Direct Sanger sequencing of viral genome populations yields multiple ambiguous sequence positions. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Inferring Short-Range Linkage Information from Sequencing Chromatograms
  19. 539
    “…Total 12 reported candidate genes were verified by Sanger sequencing. Sanger sequencing also confirmed 16 novel SNVs shared by two or more samples. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Identification of susceptibility genes in non-syndromic cleft lip with or without cleft palate using whole-exome sequencing
  20. 540
    “…In ADCs, Eprobe-PCR detected the HER2 mutation in 2.02% (9/446), while Sanger sequencing detected it in 1.57% (7/446). Eprobe-PCR was able to detect the mutation in two samples that were undetectable by Sanger sequencing. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Highly sensitive detection of a HER2 12-base pair duplicated insertion mutation in lung cancer using the Eprobe-PCR method
Herramientas de búsqueda: RSS