Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy

Biochemistry, Genetics and Molecular Biology

• Next Generation Sequencing 100%
• Nested Gene 66%
• Exon 66%
• Sequencing 66%
• Polymerase Chain Reaction 66%
• Mutation 50%
• Genotyping 33%
• Aptitude 33%
• Genetic Disorder 33%
• Hybridization 16%
• Awareness 16%
• Solution and Solubility 16%
• Time 16%

Medicine and Dentistry

• Exon 66%
• Gene 66%
• Muscular Dystrophy 50%
• Sanger Sequencing 50%
• Genetic Disorder 33%
• Genotype 33%
• Laboratory 33%
• Aptitude 33%
• Diseases 16%
• Hybridization 16%
• Awareness 16%
• Diagnosis 16%
• Sensitivity and Specificity 16%
• Reproducibility 16%
• Health Care Cost 16%
• Pseudogene 16%
• Clinician 16%
• Assessment 16%
• Muscle 16%

Neuroscience

• Exon 66%
• Gene 66%
• Muscular Dystrophy 50%
• Sanger Sequencing 50%
• Pseudogene 16%