Analyse de données NGS sous Galaxy
Module 1: Processing Raw Sequence Data
The variables for NGS experiments: coverage, read length, multiplexing
Short read" sequencing through "clustering" - France Génomique
INTRODUCTION TO NEXT GENERATION SEQUENCING
Interpreting Color by Pair Orientation | Integrative Genomics Viewer
3K Long-Tag Paired End sequencing with the Genome Sequencer FLX System | Nature Methods
Paired-End vs. Single-Read Sequencing Technology
Illumina Dye Sequencing - an overview | ScienceDirect Topics
Mate Pair Sequencing
Paired-end tag - Wikipedia
An Introduction to Next-Generation Sequencing Technology
Beyond the Linear Genome: Paired-End Sequencing as a Biophysical Tool: Trends in Cell Biology
Next Generation Sequencing - ppt download
How do you put a genome back together after sequencing? – YourGenome
Short read" sequencing through "clustering" - France Génomique
Joining Illumina paired-end reads for classifying phylogenetic marker sequences | BMC Bioinformatics | Full Text
Chapter 6: Transcriptomics – Applied Bioinformatics
What is mate pair sequencing for?
NGS data logistics
Pre-processing Paired-end Illumina data for Qiime - Bioinformatics in BioMed
Overview of Amplicon Preprocessing
