Platform comparison of detecting copy number variants with microarrays and whole-exome sequencing

Keyphrases

• Whole Exome Sequencing 100%
• Copy number Variation 100%
• Microarray 100%
• Platform Comparison 100%
• Clinically Significant 66%
• Genetic Variation 33%
• High-resolution 33%
• Intellectual Disability 33%
• Genome-wide Microarray 33%
• Point mutation 33%
• Short Reads 33%
• Complex Traits 33%
• Insertion-deletion 33%
• Copy number Variation Detection 33%
• Exome 33%
• Microarray Platform 33%
• Common Source 33%
• Genomic Disorders 33%
• Platform Software 33%
• Mendelian Disease 33%
• Detection Software 33%
• DbVar 33%

Biochemistry, Genetics and Molecular Biology

• Exome Sequencing 100%
• Microarrays 100%
• Copy-Number Variation 66%
• Genomics 66%
• Genetic Divergence 33%
• Intellectual Disability 33%
• Exome 33%
• Genetic Variation 33%
• Point Mutation 33%
• Indel 33%