Should you get sequenced? Not all bad genes predict disease
“What we really don’t know yet is whether the predictive aspects of the genome...e misconception that having the bad gene means you’re going to get the disease. That’s only true in a...3894 days ago
What Junk DNA? It’s an Operating System
The report adds to growing experimental support for the idea that all that extra stuff in t...aterial in the regulation of gene expression and its potential role in human disease.3904 days ago
RNA Sequencing Helps Identify Functional Variants from GWAS
For Alzheimer’s and other complex disorders, mining the genome for disease-associated variants is no longer the o...out how the identified loci relate to disease. As reported last month in Na...viding new tools for understanding how disease loci influence gene expressio...3808 days ago
CoronaVIR: Computational Resources on Novel Coronavirus (SARS-CoV-2 or COVID-19)
Aim of this web site is to facilitate the scientific community to fight against severe pandemic disease COVID-19 caused by SARS-CoV-2...of coronavirus, i.e. SARS-CoV-2.and its resulting disease COVID-19 from the literature...1096 days ago
SeqMule: Automated human exome/genome variants detection
SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of...t callers, and downloading databases. SeqMule can be used for both Mendelian disease study and cancer genome study...2608 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 EW...2229 days ago
NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data
NextSV, a meta SV caller and a computational pipeline to perform SV calling from low covera...bed format. Users can easily perform downstream annotation using ANNOVAR and disease gene discovery using Phenolyz...2091 days ago
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