DREAMS: Deep Read-level Error Model for Sequencing data applied to low-frequency variant calling and circulating tumor DNA detection
Mikkel Hovden Christensen, Simon Opstrup Drue, Mads Heilskov Rasmussen, Amanda Frydendahl, Iben Lyskjær, Christina Demuth, Jesper Nors, Kåre Andersson Gotschalck, Lene Hjerrild Iversen, Claus L. Andersen, Jakob Skou Pedersen
DREAMS improves variant calling and circulating tumor DNA detection by modeling sequencing errors at the read level using deep learning.
bioRxiv · Sep 27, 2022 · PreprintBioinformatics