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Research

Whole-genome variant detection in long-read sequencing data from ultra-low input patient samples

  • Katherine Wang
  • Cera J Aex
  • Hayan Lee
  • Lucas Finot
  • Kevin Zhu
  • Julianna R Chang Aaron Marks Horning William J Rowell
  • ... [+3 authors] ...,
  • Philip Li
  • Sarah Kingan
  • Michael P Snyder
  • Graham Scott Erwin
  • First Published May 28, 2026
Methods

ESPERR: Learning strong and weak signals in genomic sequence alignments to identify functional elements

  • James Taylor
  • Svitlana Tyekucheva
  • David C. King
  • Ross C. Hardison
  • Webb Miller
  • Francesca Chiaromonte
  • First Published October 19, 2006
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