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Lerna: transformer architectures for configuring error correction tools for short- and long-read genome sequencing.

Atul SharmaPranjal JainAshraf MahgoubZihan ZhouKanak MahadikSomali Chaterji
Published in: BMC bioinformatics (2022)
Lerna improves de novo genome assembly by optimizing EC tools. Our code is made available in a public repository at: https://github.com/icanforce/lerna-genomics .
Keyphrases
  • single cell
  • genome wide
  • healthcare
  • mental health
  • single molecule
  • dna methylation
  • emergency department
  • adverse drug