Keyphrases
Structural Variants
100%
Structural Variation
100%
Human Genome
100%
Whole Genome Sequencing
30%
Ultra-rare
20%
Loss Function
10%
Deleterious Effects
10%
Coding Region
10%
Computational Model
10%
Non-coding
10%
Insertion or Deletion
10%
Single nucleotide Variant
10%
Human Genetics
10%
Rare Allele
10%
Release Site
10%
Non-coding Elements
10%
Dosage Sensitivity
10%
Deletion Variant
10%
Balanced Rearrangements
10%
Gene Elements
10%
Site Frequency
10%
Function Code
10%
Complex Rearrangement
10%
Biochemistry, Genetics and Molecular Biology
Allele
100%
Whole Genome Sequencing
100%
Human Genome
100%
Single-Nucleotide Polymorphism
33%
Coding Region
33%
Human Genetics
33%