NonCode v4 database

http://m.nar.oxfordjournals.org/content/early/2013/11/26/nar.gkt1222.short?rss=1

Genome Medicine | Abstract | Efficiency of whole genome amplification of Single Circulating Tumor Cells enriched by CellSearch and sorted by FACS

http://genomemedicine.com/content/5/11/106/abstract

Fusion transcript comparison

http://link.springer.com/article/10.1186%2F1471-2105-14-S7-S2

A Lay Thesis: Maximum Likelihood Estimation - Notes, Bytes, Bases, and Plancks - Quora

Fantastic notes on MLE.

http://adarob.quora.com/A-Lay-Thesis-Maximum-Likelihood-Estimation

A Hopeful Monster: Free Resources I'd Gladly Have Paid For

http://ahopefulmonster.blogspot.com/2013/11/free-resources-id-gladly-have-paid-for.html

PLOS Computational Biology: Practical Guidelines for the Comprehensive Analysis of ChIP-seq Data

http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1003326

RNA SEQ usadellab - Trimmomatic: A flexible read trimming tool for Illumina NGS data

http://www.usadellab.org/cms/?page=trimmomatic

Microsoft - Great Projects - Human Genome Project

http://greatprojectscampaign.com/human-genome-project.html

From FastQ Data to High-Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline - Current Protocols in Bioinformatics - Auwera - Wiley Online Library

http://onlinelibrary.wiley.com/doi/10.1002/0471250953.bi1110s43/abstract;jsessionid=FF13D61431F1B7A0666A3D6C0B4173E1.f03t01

Highly expressed loci are vulnerable to misleading ChIP localization of multiple unrelated proteins

http://m.pnas.org/content/110/46/18602.abstract.html?etoc

Mosaic copy number variation in human genomes.

http://m.sciencemag.org/content/342/6158/632.short

Systematic evaluation of spliced alignment programs for RNA-seq data : Nature Methods : Nature Publishing Group

http://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.2722.html