Enhancing variant detection in complex genomes: leveraging linked reads for robust SNP, Indel, and structural variant analysis
Fields of Study & Subjects
Genomics and Phylogenetic Studies
Genomic variations and chromosomal abnormalities
Genomics and Rare Diseases
Publication details
- Journal / source
- Research Square
- Publication date
- 12 January 2026
- Language
- EN
- Document type
- Preprint