Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

3 Jul 2019

Abstract excerpt

Amyotrophic lateral sclerosis (ALS) is a rapidly progressive fatal neurodegenerative disease affecting one in 350 people. The aim of Project MinE is to elucidate the pathophysiology of ALS through whole-genome sequencing at least 15,000 ALS patients and 7500 controls at 30× coverage. Here, we present the Project MinE data browser ( databrowser.projectmine.com ), a unique and intuitive one-stop, open-access server...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyotrophic Lateral Sclerosis Research
Share to Genomics and Rare Diseases
Share to Neurogenetic and Muscular Disorders Research

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31280677
DOI: 10.1080/21678421.2019.1606244

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the publicPMID 31280677Read ↗

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the publicSemantic proximity Read ↗

Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis.Semantic proximity Read ↗

Project MinE: study design and pilot analyses of a large-scale whole genome sequencing study in amyotrophic lateral sclerosisSemantic proximity Read ↗

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA NGS data of ALS patientsSemantic proximity Read ↗

Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic VariantsSemantic proximity Read ↗

The Parkinson’s Disease DNA Variant BrowserSemantic proximity Read ↗

The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discoverySemantic proximity Read ↗

The Parkinson's Disease DNA Variant Browser.Semantic proximity Read ↗

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Semantic proximity Read ↗

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases.Semantic proximity Read ↗

Advances in sequencing technologies for amyotrophic lateral sclerosis researchSemantic proximity Read ↗

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patientsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.