Genome Regulation, Cellular Circuitry and Epigenomics. Search data, software and tools. Carlos Slim Center for Health Research. Stanley Center for Psychiatric Research. Informing Discussion on Policy Issues.

Extracting useful information from large genomic datasets. The MacArthur lab uses cutting-edge genomic technologies at massive scale to understand the impact of human genetic variation, and to provide answers to families affected by rare genetic diseases. We lead an international consortium that has assembled ExAC. Is an intuitive online portal for exploring exome and whole-genome sequencing data from rare disease families.

A blog about genomics, data science, and analysis. Get hands-on with t-SNE plots. With the growing popularity of single-cell RNA-Seq analysis, the t-SNE projection of multi-dimensional data is appearing more often in publications and online. A screen capture of the interactive t-SNE interface.

Or browse using filters and text-based search. To miRNA targets, CNVs, SNPs, GWAS associations, and more. In Correlation Engine to find those that correlate with a Meta-Analysis of up to 10 selected biosets.

Making Sense of Next-Gen Sequencing Data. The 22nd annual RECOMB 2018, one of the oldest conferences focusing on computational, mathematical, statistical and biological sciences has announced the list of accepted papers that will be presented as talks at the conference.

Diagnostics sensibles et qualité de vie. Information Security and Privacy Lab Prof. Léxico español de la alimentación y el arte culinario tradicionales. Pascal St-Amour, University of Lausanne.

Here, we summarize our current knowledge regarding the human proteome mainly achieved through antibody-based methods combined with transcriptomics analysis across all major tissues and organs of the human body. A large number of lists can be accessed with direct links to gene-specific images of the corresponding proteins in the different tissues and organs.