Sean Davis - R Tutorials

http://watson.nci.nih.gov/~sdavis/tutorials/

Identification of deleterious synonymous variants in human genomes

http://bioinformatics.oxfordjournals.org/content/early/2013/06/26/bioinformatics.btt308.short?rss=1&utm_content=buffera26e4&utm_source=buffer&utm_medium=twitter&utm_campaign=Buffer

The Human Genome Contracts Again

http://bioinformatics.oxfordjournals.org/content/early/2013/06/22/bioinformatics.btt362.short?rss=1&utm_content=buffer094f0&utm_source=buffer&utm_medium=twitter&utm_campaign=Buffer

The cancer genome in context: of mice and mutations | Cath Ennis

http://m.guardian.co.uk/science/occams-corner/2013/jun/25/cancer-genome-mice-mutations

What is sashimi_plot? — MISO 1.0 documentation

http://genes.mit.edu/burgelab/miso/docs/sashimi.html

GAT: a simulation framework for testing the association of genomic intervals

http://bioinformatics.oxfordjournals.org/content/early/2013/06/18/bioinformatics.btt343.abstract

[NGS] False Positives from Next-Gen Sequencing | MassGenomics

http://massgenomics.org/2013/06/ngs-false-positives.html

[NGS] BMC Bioinformatics | Abstract | Benchmarking short sequence mapping tools

http://www.biomedcentral.com/1471-2105/14/184/abstract

DMEAS: DNA Methylation Entropy Analysis Software

http://bioinformatics.oxfordjournals.org/content/early/2013/06/08/bioinformatics.btt332.short?rss=1

eXtasy: Variant Prioritization

http://homes.esat.kuleuven.be/~bioiuser/eXtasy/?utm_source=twitterfeed&utm_medium=twitter

BMC Genomics | Abstract | Web-based visual analysis for high-throughput genomics

http://www.biomedcentral.com/1471-2164/14/397/abstract

European Journal of Human Genetics - The Genome of the Netherlands: design, and project goals

http://www.nature.com/ejhg/journal/vaop/ncurrent/full/ejhg2013118a.html

Exome Sequencing Scientific Publications

http://www.geuvadis.org/web/geuvadis/publications;jsessionid=46779B9D0BA3B4AE322A5654480608FD

PLOS ONE: A Novel Classification of Lung Cancer into Molecular Subtypes

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0031906

The 1000 Genomes Project: paving the way for personalized genomic medicine, Personalized Medicine, Future Medicine

http://www.futuremedicine.com/doi/full/10.2217/pme.13.22

PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data

http://nar.oxfordjournals.org/content/early/2013/05/21/nar.gkt372.short?rss=1

PLOS ONE: IMSA: Integrated Metagenomic Sequence Analysis for Identification of Exogenous Reads in a Host Genomic Background

http://www.plosone.org/article/info:doi/10.1371/journal.pone.0064546