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SavvyCNV: Genome-wide CNV calling from off-target reads.

Thomas W. LaverElisa De FrancoMatthew B. JohnsonKashyap A. PatelSian EllardMichael N. WeedonSarah E. FlanaganMatthew Wakeling
Published in: PLoS Comput. Biol. (2022)
Keyphrases
  • genome wide
  • high throughput sequencing
  • high throughput
  • human genome
  • gene function
  • complex diseases
  • microarray
  • data sets
  • rna seq
  • decision trees
  • low cost
  • data processing