SIMOPAL - eine Monte Carlo Simulation des OPAL-Zentraldetektors

por Fritz, J
Publicado 1984

PhaseME: Automatic rapid assessment of phasing quality and phasing improvement

por Majidian, Sina, Sedlazeck, Fritz J
Publicado 2020

Evaluation of computational genotyping of structural variation for clinical diagnoses

por Chander, Varuna, Gibbs, Richard A, Sedlazeck, Fritz J
Publicado 2019

Bone morphogenic protein (BMP-2) enhances expression of type II collagen and aggrecan in human chondrocytes in 3D alginate cultures

por Aicher, WK, Thunemann, B, Gaissmaier, C, Fritz, J, Gründer, T
Publicado 2004

Towards population-scale long-read sequencing

por De Coster, Wouter, Weissensteiner, Matthias H., Sedlazeck, Fritz J.
Publicado 2021

PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation

por Mahmoud, Medhat, Doddapaneni, Harshavardhan, Timp, Winston, Sedlazeck, Fritz J.
Publicado 2021

Preferential production of G-CSF by a protein-like Lactobacillus rhamnosus GR-1 secretory factor through activating TLR2-dependent signaling events without activation of JNKs

por Meshkibaf, Shahab, Fritz, Jӧrg, Gottschalk, Marcelo, Kim, Sung Ouk
Publicado 2015

A multi-task convolutional deep neural network for variant calling in single molecule sequencing

por Luo, Ruibang, Sedlazeck, Fritz J., Lam, Tak-Wah, Schatz, Michael C.
Publicado 2019

Read2Tree: scalable and accurate phylogenetic trees from raw reads

por Dylus, David, Altenhoff, Adrian, Majidian, Sina, Sedlazeck, Fritz J, Dessimoz, Christophe
Publicado 2022

Multiple genome alignment in the telomere-to-telomere assembly era

por Kille, Bryce, Balaji, Advait, Sedlazeck, Fritz J., Nute, Michael, Treangen, Todd J.
Publicado 2022

Genomic variant benchmark: if you cannot measure it, you cannot improve it

por Majidian, Sina, Agustinho, Daniel Paiva, Chin, Chen-Shan, Sedlazeck, Fritz J., Mahmoud, Medhat
Publicado 2023

Adenosine deaminases that act on RNA induce reproducible changes in abundance and sequence of embryonic miRNAs

por Vesely, Cornelia, Tauber, Stefanie, Sedlazeck, Fritz J., von Haeseler, Arndt, Jantsch, Michael F.
Publicado 2012

Teaser: Individualized benchmarking and optimization of read mapping results for NGS data

por Smolka, Moritz, Rescheneder, Philipp, Schatz, Michael C., von Haeseler, Arndt, Sedlazeck, Fritz J.
Publicado 2015

Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment

por Fu, Yilei, Mahmoud, Medhat, Muraliraman, Viginesh Vaibhav, Sedlazeck, Fritz J, Treangen, Todd J
Publicado 2021

Searching thousands of genomes to classify somatic and novel structural variants using STIX

por Chowdhury, Murad, Pedersen, Brent S., Sedlazeck, Fritz J., Quinlan, Aaron R., Layer, Ryan M.
Publicado 2022

Author Correction: Searching thousands of genomes to classify somatic and novel structural variants using STIX

por Chowdhury, Murad, Pedersen, Brent S., Sedlazeck, Fritz J., Quinlan, Aaron R., Layer, Ryan M.
Publicado 2022

LRSim: A Linked-Reads Simulator Generating Insights for Better Genome Partitioning

por Luo, Ruibang, Sedlazeck, Fritz J., Darby, Charlotte A., Kelly, Stephen M., Schatz, Michael C.
Publicado 2017

Embracing the positive: an examination of how well resilience factors at age 14 can predict distress at age 17

por Fritz, J., Stochl, J., Goodyer, I. M., van Harmelen, A.-L., Wilkinson, P. O.
Publicado 2020

Rescuing Low Frequency Variants within Intra-Host Viral Populations directly from Oxford Nanopore sequencing data

por Liu, Yunxi, Kearney, Joshua, Mahmoud, Medhat, Kille, Bryce, Sedlazeck, Fritz J., Treangen, Todd J.
Publicado 2021