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Commun Biol ; 2: 147, 2019.
Article in English | MEDLINE | ID: mdl-31044172

ABSTRACT

Single-cell whole-genome sequencing (scWGS) is mainly used to probe intercellular genomic variations, focusing on the copy number variations or alterations and the single-nucleotide variations (SNVs) occurring within single cells. Single-cell whole-genome amplification (scWGA) needs to be applied before scWGS but is challenging due to the low copy number of DNA. Besides, many genomic variations are rare within a population of cells, so the throughput of currently available scWGA methods is far from satisfactory. Here, we integrate a one-step micro-capillary array (MiCA)-based centrifugal droplet generation technique with emulsion multiple displacement amplification (eMDA) and demonstrate a high-throughput scWGA method, MiCA-eMDA. MiCA-eMDA increases the single-run throughput of scWGA to a few dozen, and enables the assessment of copy number variations and alterations at 50-kb resolution. Downstream target enrichment further enables the detection of SNVs with 20% allele drop-out.


Subject(s)
Centrifugation/methods , Emulsions/chemistry , Genomics/methods , High-Throughput Nucleotide Sequencing/methods , Nucleic Acid Amplification Techniques/methods , Single-Cell Analysis/methods , Whole Genome Sequencing/methods , Alleles , DNA/genetics , DNA Copy Number Variations , Genome, Human/genetics , HeLa Cells , Humans , Lipid Droplets/chemistry , Polymorphism, Single Nucleotide
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