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SEDLAZECK, FRITZ
One or more keywords matched the following items that are connected to
SEDLAZECK, FRITZ
Item Type
Name
Concept
Software
Academic Article
Teaser: Individualized benchmarking and optimization of read mapping results for NGS data.
Academic Article
GenomeScope: fast reference-free genome profiling from short reads.
Academic Article
A multi-task convolutional deep neural network for variant calling in single molecule sequencing.
Academic Article
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.
Academic Article
Evaluation of computational genotyping of structural variation for clinical diagnoses.
Academic Article
RaGOO: fast and accurate reference-guided scaffolding of draft genomes.
Academic Article
PhaseME: Automatic rapid assessment of phasing quality and phasing improvement.
Academic Article
Parliament2: Accurate structural variant calling at scale.
Academic Article
PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation.
Academic Article
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment.
Academic Article
Searching thousands of genomes to classify somatic and novel structural variants using STIX.
Academic Article
The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms.
Academic Article
SVhound: detection of regions that harbor yet undetected structural variation.
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Software