List of works - Lukas Forer

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations

scientific article published on 12 July 2016

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

scientific article

A reference panel of 64,976 haplotypes for genotype imputation

scientific article

Association of relative telomere length with cardiovascular disease in a large chronic kidney disease cohort: the GCKD study

scientific article published on 14 August 2015

CONAN: copy number variation analysis software for genome-wide association studies

scientific article

Cloud Computing

scholarly article published 2012

Cloudflow - A framework for MapReduce pipeline development in Biomedical Research

article

Cloudflow - enabling faster biomedical pipelines with MapReduce and Spark

Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds

scientific article

Delivering bioinformatics MapReduce applications in the cloud

Do telomeres have a higher plasticity than thought? Results from the German Chronic Kidney Disease (GCKD) study as a high-risk population.

scientific article

Evaluation of gene-obesity interaction effects on cholesterol levels: a genetic predisposition score on HDL-cholesterol is modified by obesity

scientific article published on 21 September 2012

Experiences with workflows for automating data-intensive bioinformatics

scientific article

Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar

scientific article

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

scientific article

Next-generation genotype imputation service and methods

scientific article published on 29 August 2016

PedVizApi: a Java API for the interactive, visual analysis of extended pedigrees

scientific article

Reference-based phasing using the Haplotype Reference Consortium panel

scientific article published on 03 October 2016

SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.

scientific article

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

scientific article published on 6 March 2019

The power of genetic diversity in genome-wide association studies of lipids

Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.

scientific article

List of works by Lukas Forer

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

A reference panel of 64,976 haplotypes for genotype imputation

Association of relative telomere length with cardiovascular disease in a large chronic kidney disease cohort: the GCKD study

CONAN: copy number variation analysis software for genome-wide association studies

Cloud Computing

Cloudflow - A framework for MapReduce pipeline development in Biomedical Research

Cloudflow - enabling faster biomedical pipelines with MapReduce and Spark

Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds

Delivering bioinformatics MapReduce applications in the cloud

Do telomeres have a higher plasticity than thought? Results from the German Chronic Kidney Disease (GCKD) study as a high-risk population.

Evaluation of gene-obesity interaction effects on cholesterol levels: a genetic predisposition score on HDL-cholesterol is modified by obesity

Experiences with workflows for automating data-intensive bioinformatics

Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Next-generation genotype imputation service and methods

PedVizApi: a Java API for the interactive, visual analysis of extended pedigrees

Reference-based phasing using the Haplotype Reference Consortium panel

SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

The power of genetic diversity in genome-wide association studies of lipids

Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.

Visual Analytical Methods to Identify Family Clustered Diseases