BOL

Genome assembly in minutes: Deciphering the ‘book of life’ with supercomputers http://www.sciencedaily.com/releases/2015/06/150601092101.htm

Xpandomer in a single drop reaction to sequence an entire human genome 1000X over.

Researchers in Canada and the U.K. have for the first time sequenced and assembled de novo the full genome of a living organism, the bacteria Escherichia Coli, using Oxford Nanopore's MinIONTM device, a genome sequencer that can fit in the palm of...

Sequencing depth and coverage: key considerations in genomic analyses https://rtsf.natsci.msu.edu/_rtsf/assets/File/depth%20and%20coverage.pdf

Determining Exon Connectivity in Complex mRNAs by Nanopore Sequencing http://biorxiv.org/content/early/2015/05/22/019752

Sequencing ultra-long DNA molecules with the Oxford Nanopore MinION http://biorxiv.org/content/early/2015/05/20/019281.full-text.pdf+html Additional tools for analyzing Oxford Nanopore minION data by John...

Nanopore sequencing has made tremendrous progress- NEWS from London callingReceived news from a partner who participated in the London calling 2015 conference that Nanopore seq has made great progress including miniaturisation of sample preps and...

Improved data analysis for the MinION nanopore sequencer http://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.3290.html A complete bacterial genome assembled de novo using only nanopore sequencing...

Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes  http://f1000research.com/articles/4-17/v1  

Oxford Nanopore Sequencing and de novo Assembly of a Eukaryotic Genome http://biorxiv.org/content/early/2015/01/06/013490

Some useful links on Nanopore: Decoding long nanopore sequencing reads of natural DNA:http://www.nature.com/nbt/journal/v32/n8/full/nbt.2950.html Related links:- Data from pocket-sized genome sequencer unveiled...

A blog post by Aaron Krol discuss more about "Nanopore Sequencing Is Here to Stay" http://www.bio-itworld.com/2014/12/22/nanopore-sequencing-here-stay.html

User-friendly tools for the normalization and visualization of deep-sequencing data

The next generation science standards meet nanopore sequencing http://scienceblogs.com/digitalbio/2014/10/08/the-next-generation-science-standards-meet-nanopore-sequencing/

VCF parsing library https://github.com/mendelics/vcf Docs are already on the excellent godoc.org : http://godoc.org/github.com/mendelics/vcf 

HiChIP: a high-throughput pipeline for integrative analysis of ChIP-Seq data http://www.biomedcentral.com/1471-2105/15/280/abstract

dDocent: a RADseq, variant-calling pipeline designed for population genomics of non-model organisms https://peerj.com/articles/431/

VarScanvariant detection in massively parallel sequencing data http://varscan.sourceforge.net/

Few next generation sequencing resources at http://www.nature.com/subjects/next-generation-sequencing This illumina http://res.illumina.com/documents/products/illumina_sequencing_introduction.pdf intro is good for beginners.

Oxford Nanopore announced that it has raised $59 Million (£35 million) from both new and existing investors in the UK, US and mainland Europe. In its last fund raising round in 2013, Oxford Nanopore raised $64 million. These additional funds...