Publication & Citation Trends
Publications
0 total
SNP calling, haplotype phasing and allele-specific analysis with long RNA-seq reads
Cited by 0
Semantic Scholar
Using the linear references from the pangenome to discover missing autism variants
Cited by 2
Semantic Scholar
Complex genetic variation in nearly complete human genomes
Cited by 28
Semantic Scholar
Author Correction: Complex genetic variation in nearly complete human genomes
Cited by 2
Semantic Scholar
Structural variation in 1,019 diverse humans based on long-read sequencing
Cited by 39
Semantic Scholar
Structural and transduction patterns of human-specific polymorphic SVA insertions
Cited by 0
Semantic Scholar
SVarp: pangenome-based structural variant discovery
Cited by 6
Semantic Scholar
Research Topics
Genomics and Phylogenetic Studies
(35)
Genomic variations and chromosomal abnormalities
(19)
Genomics and Rare Diseases
(18)
Chromosomal and Genetic Variations
(14)
Gene expression and cancer classification
(11)
Affiliations
Research Institute of Molecular Pathology
Düsseldorf University Hospital
Max Planck Institute for Informatics
Jackson Laboratory
Klinikum Saarbrücken