Brain Dopamine–Serotonin Vesicular Transport Disease and Its Treatment.pdf
Sequential Kernel Association Tests for the Combined Effect of Rare and Common Variants Journal club (Nov/13) SH Lee.
Genetics Technology: Next Generation Sequencing in Clinical Practice Dr Yvonne Wallis FRCPath Principal Clinical Scientist Head of Familial Cancer Services
Exome Sequencing and cis-Regulatory Mapping Identify Mutations in MAK, a Gene Encoding a Regulator of Ciliary Length, as a Cause of Retinitis Pigmentosa.
Next Generation Cancer Data Discovery, Access, and Integration Using Prizms and Nanopublications
Using Public Access Clinical Databases to Interpret NGS Variants
MseqDR consortium: a grass-roots effort to establish a global resource aimed to empower genomic studies of mitochondrion diseases - Marcella Attimonelli
AGBT 2013: Home Brewed Personalized Genomics - The Quest for Meaningful Analysis Results of a 23andMe Exome Pilot Trio of Myself, Wife, and Son
Performing Small-N Sequencing Workflows: Approaches to Analyzing Trio NGS Data
Towards Precision Medicine: Tute Genomics, a cloud-based application for analysis of personal genomes
SNPs Presentation Cavalcanti Lab
El proyecto 1000 genomas
