Author

O. Distl

University of Veterinary Medicine Hannover, FoundationORCID 0000-0002-3516-836XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetics· 2 Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:variant calling· 3 Assay:whole-genome sequencing· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Organism:bacteria (other)· 1 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Julia MetzgeriD· 4 shared Carrie J. FinnoiD· 2 shared Cecilia Penedo· 2 shared Claire M. WadeiD· 2 shared Gabriella LindgreniD· 2 shared Ludovic OrlandoiD· 2 shared Molly E. McCueiD· 2 shared Ted KalbfleischiD· 2 shared

Activity by Year

2017-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

4 shared papersGenomics

Julia MetzgerORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

GenomicsbioRxivPreprintJun 7, 2022

Long-read RNA Sequencing Improves the Annotation of the Equine Transcriptome

Sichong Peng, Anna R. Dahlgren, Erin N. Hales…·Carrie J. Finno

The paper improves the equine transcriptome annotation using long-read RNA sequencing, achieving 45% better completeness and enhanced identification of alternative splicing and noncoding genes.

6 citations

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsbioRxivPreprintMar 11, 2019

De-novo variants in XIRP1 associated with polydactyly and polysyndactyly in Holstein cattle

Marina Braun, Maren Hellige, Ingo Gerhauser…·O. Distl

The paper identifies de-novo variants in XIRP1 associated with polydactyly and polysyndactyly in Holstein cattle through whole genome sequencing and bioinformatic analysis.

3 citations

bacteria (other)whole-genome sequencing

𝕏 PostBluesky

GeneticsG3 Genes Genomes GeneticsPeer-reviewedNov 5, 2018

A de novo EDA-variant in a litter of shorthaired standard Dachshunds with X-linked hypohidrotic ectodermal dysplasia

Danaë Vasiliadis, Marion Hewicker‐Trautwein, Daniela Klotz…·O. Distl

The paper identifies a de novo EDA mutation causing X-linked hypohidrotic ectodermal dysplasia in shorthaired standard Dachshunds through whole-genome sequencing and family analysis.

8 citations

Drosophilawhole-genome sequencing

𝕏 PostBluesky

GenomicsBMC GenomicsPeer-reviewedJul 27, 2017

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds

Robert Schaefer, Mikkel Schubert, Ernest Bailey…·Molly E. McCue

The paper develops two new SNP arrays for horses, MNEc2M and MNEc670k, and demonstrates their imputation capabilities.

132 citationstop 1%

whole-genome sequencingstatistical model

𝕏 PostBluesky