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Search Results to Emily G. Farrow

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Farrow, Emily

Item TypeName
Concept Genome, Human
Concept Genome
Concept Genome, Mitochondrial
Concept Genome-Wide Association Study
Academic Article Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Academic Article Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Academic Article A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases.
Academic Article Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.
Academic Article Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.
Academic Article The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Academic Article Clinical genome sequencing in an unbiased pediatric cohort.
Academic Article Next-generation community genetics for low- and middle-income countries.
Academic Article Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome.
Academic Article Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Academic Article Clinical detection of deletion structural variants in whole-genome sequences.
Academic Article Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Academic Article Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing.
Academic Article Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing.
Academic Article Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing Technologies.

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  • Genome