Pages that link to "Q30581758"
The following pages link to An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. (Q30581758):
Displaying 50 items.
- How peer-review constrains cognition: on the frontline in the knowledge sector (Q24273320) (← links)
- High-throughput sequencing technologies (Q28647379) (← links)
- The Prostate Cancer DREAM Challenge: A Community-Wide Effort to Use Open Clinical Trial Data for the Quantitative Prediction of Outcomes in Metastatic Prostate Cancer (Q28647797) (← links)
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification (Q30300875) (← links)
- A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. (Q30847688) (← links)
- Data sharing in the undiagnosed diseases network (Q30983674) (← links)
- When "N of 2" is not enough: integrating statistical and functional data in gene discovery. (Q33622353) (← links)
- Good Laboratory Standards for Clinical Next-Generation Sequencing Cancer Panel Tests. (Q33729699) (← links)
- Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding. (Q34624868) (← links)
- Next-generation sequencing in clinical oncology: next steps towards clinical validation (Q34774908) (← links)
- Living laboratory: whole-genome sequencing as a learning healthcare enterprise (Q34995956) (← links)
- Toward better benchmarking: challenge-based methods assessment in cancer genomics (Q35053798) (← links)
- Churchill: an ultra-fast, deterministic, highly scalable and balanced parallelization strategy for the discovery of human genetic variation in clinical and population-scale genomics (Q35097637) (← links)
- Clinical pertinence metric enables hypothesis-independent genome-phenome analysis for neurologic diagnosis (Q35118891) (← links)
- The road from next-generation sequencing to personalized medicine (Q35623147) (← links)
- Challenges in exome analysis by LifeScope and its alternative computational pipelines (Q35766213) (← links)
- Reliably Detecting Clinically Important Variants Requires Both Combined Variant Calls and Optimized Filtering Strategies (Q35850909) (← links)
- A rigorous approach for selection of optimal variant sets for carrier screening with demonstration of clinical utility (Q35907762) (← links)
- A genome sequencing program for novel undiagnosed diseases. (Q36074256) (← links)
- Mitigating false-positive associations in rare disease gene discovery (Q36077083) (← links)
- A framework for the detection of de novo mutations in family-based sequencing data (Q36201705) (← links)
- Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR. (Q36479375) (← links)
- RAS testing in metastatic colorectal cancer: advances in Europe (Q36795904) (← links)
- Responsible implementation of expanded carrier screening (Q36902740) (← links)
- Natural Allelic Variations in Highly Polyploidy Saccharum Complex (Q36978738) (← links)
- Integrating precision cancer medicine into healthcare-policy, practice, and research challenges (Q37360550) (← links)
- Diagnostic use of Massively Parallel Sequencing in Neuromuscular Diseases: Towards an Integrated Diagnosis (Q37589634) (← links)
- Blind prediction of deleterious amino acid variations with SNPs&GO. (Q38437989) (← links)
- Exome sequencing explained: a practical guide to its clinical application (Q38665695) (← links)
- Clinical exome sequencing reports: current informatics practice and future opportunities (Q38680198) (← links)
- Principles of analytical validation of next-generation sequencing based mutational analysis for hematologic neoplasms in a CLIA-certified laboratory. (Q38696183) (← links)
- Genetics of movement disorders in the next-generation sequencing era. (Q38743361) (← links)
- Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL. (Q38966415) (← links)
- Promises and pitfalls of Illumina sequencing for HIV resistance genotyping (Q39043678) (← links)
- Critical points for an accurate human genome analysis. (Q39283243) (← links)
- Biocompute Objects-A Step towards Evaluation and Validation of Biomedical Scientific Computations. (Q41016745) (← links)
- M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity (Q46384543) (← links)
- Benchmarking distributed data warehouse solutions for storing genomic variant information (Q47113794) (← links)
- Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers. (Q47215728) (← links)
- Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis (Q47770082) (← links)
- Settling the score: variant prioritization and Mendelian disease. (Q52544730) (← links)
- Enhancing genomic laboratory reports from the patients' view: A qualitative analysis. (Q53463935) (← links)
- Systematic review of innovation design contests for health: spurring innovation and mass engagement. (Q53601607) (← links)
- Enhancing genomic laboratory reports: A qualitative analysis of provider review. (Q55037100) (← links)
- Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics. (Q55384079) (← links)
- Recent developments in genetics and medically assisted reproduction: from research to clinical applications (Q56927575) (← links)
- An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery (Q57646244) (← links)
- Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR (Q57646321) (← links)
- Recent developments in genetics and medically-assisted reproduction: from research to clinical applications†‡ (Q93118941) (← links)
- Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study (Q99568795) (← links)