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Detection of copy number alterations by shallow whole-genome sequencing of formalin-fixed, paraffin-embedded tumor tissue
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PCR based target enrichment for variant confirmation, gene panels and multiplex PCR sample tracking in a whole exome sequencing workflow
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- Journal Article
- A1
- open access
Preface : in silico pipeline for accurate cell-free fetal DNA fraction prediction
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- Journal Article
- A1
- open access
WisecondorX : improved copy number detection for routine shallow whole-genome sequencing
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Detection of copy number alterations using shallow whole genome sequencing on formalin-fixed paraffin-embedded tumor tissue
-
Detection of copy number alterations using shallow whole genome sequencing on formalin-fixed paraffin-embedded tumor tissue
-
- Journal Article
- A1
- open access
Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory