December 2011
15 posts
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing : Nature Biotechnology : Nature Publishing Group http://ping.fm/DnXWa
BMC Bioinformatics | GC-Content Normalization for RNA-Seq Data http://ping.fm/95KVF
A computational pipeline for comparative ChIP-seq analyses : Nature Protocols http://ping.fm/j0uSD
A computational pipeline for comparative ChIP-seq analyses : Nature Protocols http://ping.fm/24rWi
Performance comparison of whole-genome sequencing platforms : Nature Biotechnology http://ping.fm/13oPg
Sparse linear modeling of next-generation mRNA sequencing (RNA-Seq) data for isoform discovery and abundance estimation http://ping.fm/Q9rFp
Aiming for Q2 2012 Launch, GnuBio Builds Beta Version of Microfluidics-Based Sequencing System http://ping.fm/8ObdH
Find Your Inner Neanderthal http://ow.ly/1C8S0d (via @23andMe)
Next-generation sequencing for cancer diagnostics: a practical perspective. http://ping.fm/7iJiX
How $10 million sparks innovation - CNN.com http://ping.fm/Hb2MK
Identification and correction of systematic error in high-throughput sequence data http://ping.fm/Bx25Q
Assemblathon 1: A competitive assessment of de novo short read assembly methods http://ping.fm/sU9Le
Differential expression in RNA-seq: A matter of depth http://ping.fm/O1hkm
DNA Sequencing Caught in Deluge of Data - NYTimes.com http://ping.fm/mHXnq
Making next-generation sequencing analysis pipelines easier with BioCloudCentral and Galaxy integration « Blue Collar Bioinformatics http://ping.fm/oZC7h