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Uncovering low-level mosaicism in human embryonic stem cells using high throughput single cell shallow sequencing
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Chromosomal mosaicism in human blastocysts : the ultimate challenge of preimplantation genetic testing?
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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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Performance of four modern whole genome amplification methods for copy number variant detection in single cells
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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
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Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method