Should you get sequenced? Not all bad genes predict disease
...we roll out genomic medicine we are fighting against this society-wide misconception that having the bad gene means you’re going to get the disease. That’s only true in a...3884 days ago
What Junk DNA? It’s an Operating System
...growing body of knowledge establishing a considerable role for this material in the regulation of gene expression and its potential role in human disease.3894 days ago
RNA Sequencing Helps Identify Functional Variants from GWAS
...ther complex disorders, mining the genome for disease-associated variants is no lon...iguring out how the identified loci relate to disease. As reported last month in Na...are providing new tools for understanding how disease loci influence gene expressio...3799 days ago
CoronaVIR: Computational Resources on Novel Coronavirus (SARS-CoV-2 or COVID-19)
...o facilitate the scientific community to fight against severe pandemic disease COVID-19 caused by SARS-CoV-2...ated to novel strain of coronavirus, i.e. SARS-CoV-2.and its resulting disease COVID-19 from the literature...1087 days ago
SeqMule: Automated human exome/genome variants detection
...callers, plotting a Venn diagram showing intersection among different callers, and downloading databases. SeqMule can be used for both Mendelian disease study and cancer genome study...2599 days ago
EWAS: epigenome-wide association study software 2.0
EWAS2.0 can analyze EWAS data and identify the association between epigenetic variations and disease/phenotype. On the basis of EWAS1.0, we have added more distinctive features. EWAS2...2219 days ago
NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data
...rent analysis purpose. The output of NextSV is in ANNOVAR-compatible bed format. Users can easily perform downstream annotation using ANNOVAR and disease gene discovery using Phenolyz...2081 days ago
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