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Biomed Research International|July 3, 2015
DNAseq Workflow in a Diagnostic Context and an Example of a User Friendly ImplementationBeat Wolf, Pierre Kuonen, Thomas Dandekar, et al.Thrombosis and Haemostasis|May 8, 2015
Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII geneJ Elisa Bach, Beat Wolf, Johannes Oldenburg, et al.Genetics|October 17, 2020
Detecting Selection from Linked Sites Using an F-ModelMarco Galimberti, Christoph Leuenberger, Beat Wolf, et al.Genes|December 31, 2016
Non-Coding RNAs in Lung Cancer: Contribution of Bioinformatics Analysis to the Development of Non-Invasive Diagnostic ToolsMeik Kunz, Beat Wolf, Harald Schulze, et al.Briefings in Bioinformatics|October 4, 2019
A comprehensive method protocol for annotation and integrated functional understanding of lncRNAsMeik Kunz, Beat Wolf, Maximilian Fuchs, et al.International Journal of Cancer|April 17, 2018
Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patientsJulia Böck, Silke Appenzeller, Larissa Haertle, et al.International Journal of Molecular Sciences|September 9, 2023
Whole-Genome Sequencing Identified New Structural Variations in the DMD Gene That Cause Duchenne Muscular Dystrophy in Two GirlsNatalie Pluta, Arpad von Moers, Astrid Pechmann, et al.Genes|October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular DystrophyNatalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.Pageof 1