Keyphrases
4-fold
11%
Amplification Artefacts
11%
Aneuploidy
22%
Base-resolution
11%
Breadth of Coverage
11%
Cause of Disease
11%
Clinical Grade
100%
Consanguineous
11%
DNA Samples
11%
Genetic Abnormalities
11%
Genetic Variants
11%
Genotyping-by-sequencing
22%
Haplarithmisis
100%
High-throughput Sequencing
11%
In Vitro Embryo Production
22%
Indel
11%
Mitochondrial DNA
22%
Multi-cell
11%
Nuclear DNA (nDNA)
22%
Pathogenic CNV
16%
PCR-based
11%
Preimplantation Genetic Diagnosis
100%
Preimplantation Genetic Testing for Monogenic Disorders (PGT-M)
11%
Single nucleotide Variant
11%
Structural Rearrangement
11%
Translocation Breakpoint
11%
Turnaround Time
11%
Wet Laboratory
11%
Whole Genome Amplification
11%
Whole Genome Sequencing
100%
INIS
algorithms
25%
amplification
8%
aneuploidy
16%
comparative evaluations
8%
data
50%
datasets
12%
diseases
58%
dna
33%
embryos
29%
enrichment
12%
europe
12%
genes
12%
genetics
100%
in vitro
16%
increasing
8%
labor
8%
mitochondria
25%
nucleotides
8%
origin
8%
pcr
8%
resolution
8%
sensitivity
12%
testing
100%
translocation
8%
values
12%
Biochemistry, Genetics and Molecular Biology
Aneuploidy
20%
Exome Sequencing
50%
Gene Amplification
10%
Genetic Divergence
10%
Genetic Screening
100%
Genetics
10%
Genotyping
20%
High Throughput Sequencing
10%
Indel
10%
Mitochondrial DNA
20%
Nuclear DNA
20%
Overlapping Gene
50%
Preimplantation
100%
Single-Nucleotide Polymorphism
10%
Turnaround Time
10%
Whole Genome Sequencing
100%
