Next Gen Sequenci...
Follow
Find
5.3K views | +0 today
Next Gen Sequencing (NGS) and Bioinformatics at UVic
Your new post is loading...
Your new post is loading...
Scooped by Chris Upton + helpers
Scoop.it!

BMC Bioinformatics | Abstract | A new strategy for better genome assembly from very short reads

With the rapid development of the next generation sequencing (NGS) technology, large quantities of genome sequencing data have been generated.
more...
No comment yet.
Scooped by Nik Veldhoen
Scoop.it!

RNA-Seq: a revolutionary tool for transcriptom... [Nat Rev Genet. 2009] - PubMed - NCBI

This article describes the RNA-Seq approach, the challenges associated with its application, and the advances made so far in characterizing several eukaryote transcriptomes.

more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

PLoS ONE: myKaryoView: A Light-Weight Client for Visualization of Genomic Data

PLoS ONE: myKaryoView: A Light-Weight Client for Visualization of Genomic Data | Next Gen Sequencing (NGS) and Bioinformatics at UVic | Scoop.it
PLoS ONE: an inclusive, peer-reviewed, open-access resource from the PUBLIC LIBRARY OF SCIENCE. Reports of well-performed scientific studies from all disciplines freely available to the whole world.
more...
No comment yet.
Scooped by Nik Veldhoen
Scoop.it!

Next-generation transcriptome assembly. [Nat Rev Genet. 2011] - PubMed - NCBI

This Review summarizes the recent developments in transcriptome assembly approaches - reference-based, de novo and combined strategies - along with some perspectives on transcriptome assembly in the near future.

more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

BMC Bioinformatics | Abstract | An integrative variant analysis suite for whole exome next-generation sequencing data

Whole exome capture sequencing allows researchers to cost-effectively sequence the coding regions of the genome.
more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

What is going on with 454 GS FLX+ sequencing?

Supposedly, if you need long reads of high quality and throughput, you should be using GS FLX+, yielding 750-800 peak read length, from Roche/454, right? Illumina reads are getting longer, but 250 ...
more...
No comment yet.
Rescooped by Chris Upton + helpers from Virology and Bioinformatics from Virology.ca
Scoop.it!

iPhylo: Open course on phyloinformatics

iPhylo: Open course on phyloinformatics | Next Gen Sequencing (NGS) and Bioinformatics at UVic | Scoop.it
more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

PLoS Computational Biology: A Quick Guide for Developing Effective Bioinformatics Programming Skills

PLoS Computational Biology is an open-access...
more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

When is a genome finished?

A retrospective look at the state of many famous modern genome sequences, and a cautionary tale of the dangers in assuming that genome sequence and/or its annot ('When is a genome finished?
more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

Ngs Summer Course 2012 - MSU Bioinformatics

Analyzing Next-Generation Sequencing Data

June 4th - June 15th, 2012
Kellogg Biological Station, MSU

more...
No comment yet.
Scooped by Chris Upton + helpers
Scoop.it!

From genomics to metagenomics 10.1016/j.copbio.2011.12.017 : Current Opinion in Biotechnology | ScienceDirect.com

more...
No comment yet.
Rescooped by Chris Upton + helpers from Virology and Bioinformatics from Virology.ca
Scoop.it!

NARWHAL, a primary analysis pipeline for NGS data

Summary: The NARWHAL software pipeline has been developed to automate the primary analysis of Illumina sequencing data. This pipeline combines a new and flexible de-multiplexing tool with open-source aligners and automated quality assessment. The entire pipeline can be run using only one simple sample-sheet for diverse sequencing applications. NARWHAL creates a sample-oriented data structure and outperforms existing tools in speed.

Availability: https://trac.nbic.nl/narwhal/

more...
No comment yet.