DNA qualification workflow for next generation sequencing of histopathological samples.
about
Technological considerations for genome-guided diagnosis and management of cancerStandardization and quality management in next-generation sequencingSystematic evaluation of sericin protein as a substitute for fetal bovine serum in cell cultureTargeted next-generation sequencing of cancer genes dissects the molecular profiles of intraductal papillary neoplasms of the pancreas.Multigene mutational profiling of cholangiocarcinomas identifies actionable molecular subgroups.Reporting tumor molecular heterogeneity in histopathological diagnosis.Highly sensitive amplicon-based transcript quantification by semiconductor sequencingComparison of pre-analytical FFPE sample preparation methods and their impact on massively parallel sequencing in routine diagnosticsVariation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial.Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples.Molecular heterogeneity assessment by next-generation sequencing and response to gefitinib of EGFR mutant advanced lung adenocarcinoma.Pitfalls of DNA Quantification Using DNA-Binding Fluorescent Dyes and Suggested SolutionsNext-generation sequencing for genetic testing of familial colorectal cancer syndromes.Quantitation of next generation sequencing library preparation protocol efficiencies using droplet digital PCR assays - a systematic comparison of DNA library preparation kits for Illumina sequencingUse of the melting curve assay as a means for high-throughput quantification of Illumina sequencing libraries.Performance Characterization and Validation of Saliva as an Alternative Specimen Source for Detecting Hereditary Breast Cancer Mutations by Next Generation Sequencing.Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing.Highly sensitive and quantitative evaluation of the EGFR T790M mutation by nanofluidic digital PCR.Next-Generation Sequencing Workflow for NSCLC Critical Samples Using a Targeted Sequencing Approach by Ion Torrent PGM™ Platform.Comprehensive molecular portrait using next generation sequencing of resected intestinal-type gastric cancer patients dichotomized according to prognosis.Genome-Wide Transcriptional Excavation of Dipsacus asperoides Unmasked both Cryptic Asperosaponin Biosynthetic Genes and SSR Markers.BRCA somatic and germline mutation detection in paraffin embedded ovarian cancers by next-generation sequencingDNA Source Selection for Downstream Applications Based on DNA Quality Indicators AnalysisSingle nucleotide polymorphisms to discriminate different classes of hybrid between wild Atlantic salmon and aquaculture escapeesRoutine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms.Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsiesTissue recommendations for precision cancer therapy using next generation sequencing: a comprehensive single cancer center's experiences.[Revision arthroplasty : Histopathological diagnostics in periprosthetic joint infections].Quantification of DNA Extracted from Formalin Fixed Paraffin-Embeded Tissue Comparison of Three Techniques: Effect on PCR EfficiencyA Microneedle Functionalized with Polyethyleneimine and Nanotubes for Highly Sensitive, Label-Free Quantification of DNA.Lung neuroendocrine tumours: deep sequencing of the four World Health Organization histotypes reveals chromatin-remodelling genes as major players and a prognostic role for TERT, RB1, MEN1 and KMT2D.Hajdu Cheney Syndrome; report of a novel NOTCH2 mutation and treatment with denosumabMulticenter validation of cancer gene panel-based next-generation sequencing for translational research and molecular diagnostics.Young investigator challenge: Can the Ion AmpliSeq Cancer Hotspot Panel v2 be used for next-generation sequencing of thyroid FNA samples?Isolation of Wheat Genomic DNA for Gene Mapping and Cloning.DNA degrades during storage in formalin-fixed and paraffin-embedded tissue blocks.Progress and potential of RAS mutation detection for diagnostics and companion diagnostics.Cholangiocarcinoma Heterogeneity Revealed by Multigene Mutational Profiling: Clinical and Prognostic Relevance in Surgically Resected Patients.High-throughput mutation profiling improves diagnostic stratification of sporadic medullary thyroid carcinomas.High-throughput mutation profiling identifies novel molecular dysregulation in high-grade intraepithelial neoplasia and early gastric cancers.
P2860
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P2860
DNA qualification workflow for next generation sequencing of histopathological samples.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
DNA qualification workflow for next generation sequencing of histopathological samples.
@ast
DNA qualification workflow for next generation sequencing of histopathological samples.
@en
DNA qualification workflow for next generation sequencing of histopathological samples.
@nl
type
label
DNA qualification workflow for next generation sequencing of histopathological samples.
@ast
DNA qualification workflow for next generation sequencing of histopathological samples.
@en
DNA qualification workflow for next generation sequencing of histopathological samples.
@nl
prefLabel
DNA qualification workflow for next generation sequencing of histopathological samples.
@ast
DNA qualification workflow for next generation sequencing of histopathological samples.
@en
DNA qualification workflow for next generation sequencing of histopathological samples.
@nl
P2860
P50
P1433
P1476
DNA qualification workflow for next generation sequencing of histopathological samples.
@en
P2093
Marisa Gottardi
P2860
P304
P356
10.1371/JOURNAL.PONE.0062692
P407
P50
P577
2013-06-06T00:00:00Z