Mehmet Tekman

发表

OVAS: an open-source variant analysis suite with inheritance modelling

Monika Mozere, Mehmet Tekman, Jameela Kari, 2018, BMC Bioinformatics.

HaploForge: a comprehensive pedigree drawing and haplotype visualization web application

Alan Medlar, Monika Mozere, Mehmet Tekman, 2017, Bioinform..

Training material for single-cell RNA-seq data analysis (Galaxy Training Network tutorial)

Mehmet Tekman, 2018 .

Updates from the Single-Cell Community

Mehmet Tekman, Wendi Bacon, 2021 .

Galaxy Training Material for single-cell RNA-seq tutorial with Plant Datasets

Mehmet Tekman, 2021 .

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Deborah Hughes, Christine Klein, Thomas Foltynie, 2015, American journal of human genetics.