Pages that link to "Q38115273"
Jump to navigation
Jump to search
The following pages link to Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories (Q38115273):
Displaying 44 items.
- Quality standards for DNA sequence variation databases to improve clinical management under development in Australia (Q24658490) (← links)
- Novel bioinformatic developments for exome sequencing (Q24658618) (← links)
- Challenges of Identifying Clinically Actionable Genetic Variants for Precision Medicine (Q28596030) (← links)
- Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects (Q28610872) (← links)
- Returning findings within longitudinal cohort studies: the 1958 birth cohort as an exemplar (Q34040535) (← links)
- Diagnostics of primary immunodeficiency diseases: a sequencing capture approach (Q34681895) (← links)
- Next-generation sequencing in clinical oncology: next steps towards clinical validation (Q34774908) (← links)
- Application of Next Generation Sequencing for personalized medicine for sudden cardiac death (Q35135586) (← links)
- A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape (Q36239238) (← links)
- panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics (Q36356887) (← links)
- Targeted resequencing and variant validation using pxlence PCR assays (Q36769289) (← links)
- RAS testing in metastatic colorectal cancer: advances in Europe (Q36795904) (← links)
- Responsible implementation of expanded carrier screening (Q36902740) (← links)
- Techniques and Approaches to Genetic Analyses in Nephrological Disorders (Q37032666) (← links)
- BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency (Q37042363) (← links)
- Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer. (Q37554531) (← links)
- Contribution of high-throughput DNA sequencing to the study of primary immunodeficiencies (Q38243005) (← links)
- Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics (Q38289442) (← links)
- Assessment of concordance between fresh-frozen and formalin-fixed paraffin embedded tumor DNA methylation using a targeted sequencing approach (Q38373884) (← links)
- Advances in clinical next-generation sequencing: target enrichment and sequencing technologies (Q38672934) (← links)
- Advances in renal genetic diagnosis (Q38673027) (← links)
- Principles of analytical validation of next-generation sequencing based mutational analysis for hematologic neoplasms in a CLIA-certified laboratory. (Q38696183) (← links)
- Defining the Clinical Value of a Genomic Diagnosis in the Era of Next-Generation Sequencing. (Q38846804) (← links)
- Critical points for an accurate human genome analysis. (Q39283243) (← links)
- Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing (Q39393194) (← links)
- Next-generation diagnostics: gene panel, exome, or whole genome? (Q41220493) (← links)
- The future of Clinical Utility Gene Cards in the context of next-generation sequencing diagnostic panels. (Q42548665) (← links)
- Targeted next-generation sequencing panels for monogenetic disorders in clinical diagnostics: the opportunities and challenges (Q43580712) (← links)
- High Throughput Sequencing for Detection of Foodborne Pathogens. (Q46090917) (← links)
- Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers. (Q47215728) (← links)
- A post hoc study on gene panel analysis for the diagnosis of dystonia (Q47235303) (← links)
- Points to consider for laboratories reporting results from diagnostic genomic sequencing (Q47400714) (← links)
- Next-Generation Sequencing in Diagnostic Pathology (Q47609024) (← links)
- Genetic diagnostics of inherited aortic diseases : Medical strategy analysis (Q48788951) (← links)
- Paediatric genomics: diagnosing rare disease in children (Q49339134) (← links)
- Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. (Q49912348) (← links)
- European guidelines for constitutional cytogenomic analysis (Q57054917) (← links)
- [Genetic testing to prevent sudden cardiac death] (Q57172466) (← links)
- A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases (Q57536768) (← links)
- Identification of Factors Affecting the Success of Next-Generation Sequencing Testing in Solid Tumors (Q58001833) (← links)
- Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors' and counselees' views (Q64121288) (← links)
- The missing heritability of familial colorectal cancer (Q90666764) (← links)
- Pharmacogenomic Testing: Clinical Evidence and Implementation Challenges (Q92503675) (← links)
- National external quality assessment for next-generation sequencing-based diagnostics of primary immunodeficiencies (Q98177220) (← links)