Bioinformatics | Computer Science | Genomics NPSV-deep: a deep learning method for genotyping structural variants in short read genome sequencing data. March 6, 2024
Other Automated filtering of genome-wide large deletions through an ensemble deep learning framework. August 29, 2022
Bioinformatics | Genomics Sequence-based modeling of three-dimensional genome architecture from kilobase to chromosome scale. May 13, 2022
Genomic Medicine | Psychiatry Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients. January 8, 2022
Bioinformatics | Genomics DeepSVP: Integration of genotype and phenotype for structural variant prioritization using deep learning. December 24, 2021
Bioinformatics | Clinical Genetics | Genetics A deep learning approach for filtering structural variants in short read sequencing data. December 30, 2020