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Hi Alok,

In general NGS is a wide term to use, I will recommend you to start reading some papers related to a specific argument ( google return about 455,000 results for 'NGS tutorial').

Does anyone know where I could start?

I think quality control(QC) is the basic to start with. The QC, trimming and masking of the bad nucleotides of the reads that you want to align and later analyse is very important ( ftp://ftp-mouse.sanger.ac.uk/other/tk2/ECCB/ECCB-tutorial-thomas1.pdf ). I will also recommend to check/read the limitation of various NGS technologies.

Following links afford some questions:

http://users.ugent.be/~avierstr/nextgen/Next_generation_sequencing_web.pdf
http://lpm.hms.harvard.edu/palaver/sites/default/files/11_02_28_Dennis_Wall_1.pdf
http://ngs-expert.com/tag/tutorial/

Cheers

Hi Alok,

You can find several useful bookmarked online NGS tutorial links at http://bioinformaticsonline.com/bookmarks/view/3868/next-generation-sequencing-ngs-tutorials

Cheers

Hi Alok,

NGS Family Analysis Tutorial by Golden Helix is much useful and user friendly. http://doc.goldenhelix.com/SVS/tutorials/ngs_family_analysis/ngs_family_analysis.pdf

GATB: Genome Assembly & Analysis Tool Box is yet another useful resource. http://bioinformatics.oxfordjournals.org/content/early/2014/07/12/bioinformatics.btu406.full

The RNAseq toolbox for other useful resources http://wiki.bits.vib.be/index.php/RNAseq_toolbox

Thanks