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- Journal Article
- A1
- open access
Short tandem repeat analysis after whole genome amplification of single B-lymphoblastoid cells
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- Journal Article
- A1
- open access
Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes : a comparative evaluation of upstream whole-genome amplification methods
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- PhD Thesis
- open access
Massively parallel sequencing in preimplantation and prenatal genetic diagnosis
(2017) -
- Journal Article
- A1
- open access
STR profiling and Copy Number Variation analysis on single, preserved cells using current Whole Genome Amplification methods
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- Journal Article
- A1
- open access
Performance of four modern whole genome amplification methods for copy number variant detection in single cells
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- Journal Article
- A1
- open access
Forensic SNP genotyping using nanopore MinION sequencing
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Preimplantation genetic diagnosis (PGD) for translocation carriers using whole genome screening by microarray analysis at the blastocyst stage
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- Journal Article
- A1
- open access
Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing
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Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts
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- Journal Article
- A1
- open access
Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method