Detection of rare genomic variants from pooled sequencing using SPLINTER

Keyphrases

• Genomic Variants 100%
• Pooled Sequencing 100%
• Genomic Loci 60%
• Complex Phenotypes 40%
• Genetic Variation 40%
• Sequencing Library 40%
• Common Disease 20%
• Amplicon 20%
• Tumor DNA 20%
• High Specificity 20%
• Missing Heritability 20%
• Sequence Analysis 20%
• Rare Variants 20%
• High Sensitivity 20%
• Array-based 20%
• Phenotypic Variation 20%
• Multi-target 20%
• Novel Variants 20%
• Variant Calling 20%
• Insertion-deletion 20%
• Sequence Variants 20%
• Optimal Performance 20%
• Control Strategy 20%
• Computational Analysis 20%
• Hybrid Capture 20%
• Individual-specific 20%
• Number of Individuals 20%
• Mutant Alleles 20%
• Highly Accurate 20%
• Rare Variation 20%
• Population Survey 20%
• Heterogeneous Samples 20%
• Sequence Coverage 20%
• DNA Sequencing Technology 20%
• Rare Variant Detection 20%
• Single Sample 20%
• Genome-wide Microarray 20%
• Personal Profile 20%
• Specific Barcode 20%

Biochemistry, Genetics and Molecular Biology

• Genomics 100%
• Genetic Divergence 50%
• Allele 50%
• Genetic Variation 50%
• Genotyping 50%
• Rare Variant 50%
• Amplicon 25%
• DNA Sequence 25%
• Indel 25%