Connection | Profiles RNS

Search Result Details

Back to Search Results

This page shows the details of why an item matched the keywords from your search.

Search Results

SEDLAZECK, FRITZ

One or more keywords matched the following items that are connected to SEDLAZECK, FRITZ

Item Type	Name
Concept	Genomics
Academic Article	Benefit-of-doubt (BOD) scoring: a sequencing-based method for SNP candidate assessment from high to medium read number data sets.
Academic Article	NextGenMap: fast and accurate read mapping in highly polymorphic genomes.
Academic Article	Teaser: Individualized benchmarking and optimization of read mapping results for NGS data.
Academic Article	The pineapple genome and the evolution of CAM photosynthesis.
Academic Article	Phased diploid genome assembly with single-molecule real-time sequencing.
Academic Article	The genomic basis of circadian and circalunar timing adaptations in a midge.
Academic Article	Piercing the dark matter: bioinformatics of long-range sequencing and mapping.
Academic Article	Accurate detection of complex structural variations using single-molecule sequencing.
Academic Article	A multi-task convolutional deep neural network for variant calling in single molecule sequencing.
Academic Article	A Genocentric Approach to Discovery of Mendelian Disorders.
Academic Article	RaGOO: fast and accurate reference-guided scaffolding of draft genomes.
Academic Article	Structural variant calling: the long and the short of it.
Academic Article	Discovery and population genomics of structural variation in a songbird genus.
Academic Article	Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes.
Academic Article	PhaseME: Automatic rapid assessment of phasing quality and phasing improvement.
Academic Article	Parliament2: Accurate structural variant calling at scale.
Academic Article	Author Correction: Discovery and population genomics of structural variation in a songbird genus.
Academic Article	Towards population-scale long-read sequencing.
Academic Article	Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment.
Academic Article	Hidden biases in germline structural variant detection.
Academic Article	A complete reference genome improves analysis of human genetic variation.
Academic Article	Fully resolved assembly of Cryptosporidium parvum.
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	Multiple genome alignment in the telomere-to-telomere assembly era.
Academic Article	FixItFelix: improving genomic analysis by fixing reference errors.
Academic Article	The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models.
Academic Article	Variant calling and benchmarking in an era of complete human genome sequences.
Academic Article	Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes.
Academic Article	The complete sequence of a human Y chromosome.
Academic Article	Genomic variant benchmark: if you cannot measure it, you cannot improve it.
Academic Article	Improved sequence mapping using a complete reference genome and lift-over.

Search Criteria

Genomics