Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine

http://genomemedicine.com/content/6/1/5

COHCAP: CpG Island Analysis for Illumina Methylation Array and Targeted BS-Seq Data - BioStar

http://www.biostars.org/p/92033/

Cell - Mapping Rare and Common Causal Alleles for Complex Human Diseases

http://www.cell.com/abstract/S0092-8674(11)01069-5?switch=standard

RNA-seq differential expression studies: more sequence or more replication?

http://m.bioinformatics.oxfordjournals.org/content/30/3/301.short?rss=1

Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster

http://m.genome.cshlp.org/content/early/2014/01/02/gr.163832.113?utm_source=twitterfeed&utm_medium=twitter

What is the True Computing Cost of RNAseq Analysis? - Titus Brown's Slides - Homologus

http://www.homolog.us/blogs/blog/2014/01/18/rnaseq-good-slides-titus-brown/

Learn R - DataCamp Beta

https://www.datacamp.com/

Somatic mitochondrial DNA mutations are associated with progression, metastasis and death in oral squamous cell carcinoma | bioRxiv

http://biorxiv.org/content/early/2014/01/24/002055

Human Genomics | Abstract | A survey of software for genome-wide discovery of differential splicing in RNA-Seq data

http://www.humgenomics.com/content/8/1/3/abstract

Faster BAM Sorting with SAMtools and RocksDB

http://devblog.dnanexus.com/faster-bam-sorting-with-samtools-and-rocksdb/

Cell - A Polymorphism in IRF4 Affects Human Pigmentation through a Tyrosinase-Dependent MITF/TFAP2A Pathway

http://www.cell.com/abstract/S0092-8674(13)01298-1