Publications by authors named "David Atlan"

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Whole-Genome Sequencing Identified New Structural Variations in the Gene That Cause Duchenne Muscular Dystrophy in Two Girls.
Natalie Pluta, Arpad von Moers, Astrid Pechmann, Werner Stenzel, Hans-Hilmar Goebel, David Atlan

Int J Mol Sci· September 2023

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Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy.
Natalie Pluta, Sabine Hoffjan, Frederic Zimmer, Cornelia Köhler, Thomas Lücke, David Atlan

Genes (Basel)· September 2022

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A comprehensive method protocol for annotation and integrated functional understanding of lncRNAs.
Meik Kunz, Beat Wolf, Maximilian Fuchs, Jan Christoph, Ke Xiao, David Atlan

Brief Bioinform· July 2020

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Non-Coding RNAs in Lung Cancer: Contribution of Bioinformatics Analysis to the Development of Non-Invasive Diagnostic Tools.
Meik Kunz, Beat Wolf, Harald Schulze, David Atlan, Thorsten Walles

Genes (Basel)· December 2016

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DNAseq Workflow in a Diagnostic Context and an Example of a User Friendly Implementation.
Beat Wolf, Pierre Kuonen, Thomas Dandekar, David Atlan

Biomed Res Int· March 2016

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Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contexts.
Owen Lancaster, Tim Beck, David Atlan, Morris Swertz, Dhiwagaran Thangavelu

Hum Mutat· October 2015

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VarioML framework for comprehensive variation data representation and exchange.
Myles Byrne, Ivo Fac Fokkema, Owen Lancaster, Tomasz Adamusiak, Anni Ahonen-Bishopp, David Atlan

BMC Bioinformatics· October 2012

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