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Mosaic autosomal aneuploidies are detectable from single-cell RNAseq data.

Jonathan A GriffithsAntonio ScialdoneJohn C Marioni
Published in: BMC genomics (2017)
The method is quick and easy to apply, straightforward to interpret, and represents a substantial cost saving compared to single-cell genome sequencing techniques. However, the method is less well suited to data where gene expression is highly variable. The results obtained from the method can be used to investigate the consequences of aneuploidy itself, or to exclude aneuploidy-affected expression values from conventional scRNA-seq data analysis.
Keyphrases
  • single cell
  • data analysis
  • rna seq
  • gene expression
  • high throughput
  • electronic health record
  • poor prognosis
  • big data
  • dna methylation
  • genome wide
  • binding protein
  • artificial intelligence