Hi Yan,
I know that you have already start this analysis with one method, as
posted here:
http://gmod.827538.n3.nabble.com/How-to-extract-geneID-from-pileup-file-tp4036039.html
But I wanted to follow-up and let you know that there are actually many
ways to go about doing this in Galaxy. Which is best can subjective,
although when working with DNA - use tools for DNA, when you have RNA -
use tools for RNA (in particular mapping tools!).
I'll group by step.
*Alignments*:
BWA and Bowtie2/Tophat2 are good choices. Bowtie/Tophat would be less
desirable (do not call indels as well). Reading each tools
documentation, or searching seqanswers for discussions on the subject
will give anyone a good idea about why - but the final call is yours -
use what works for you.
*Calling/Filtering Variants:*
Freebayes, Pileup/Mpileup, other tools in 'NGS: SAM Tools' that
filter/convert pileup files
Tools in 'NGS: Indel Analysis' - 'snpEff' - 'GATK (beta) - 'Genome
Diversity' - 'NGS: Variant Detection'
*
**Annotating Variants:*
SNPEff, new Galaxy team's tools "Naive Variant Detector" and "Variant
Annotator"
Many tools in the same tool groups above
Some of these tools are on Test https://test.g2.bx.psu.edu and/or
require a cloud Galaxy instance because of intensive compute
requirements http://wiki.galaxyproject.org/Cloud. Local or Slipstream
are also options.
Hope this helps you and others thinking about this sort of analysis!
Jen
Galaxy team
On 8/22/13 6:37 PM, Yan He wrote:
Hi Jen and other Galaxy-users,
I am working on exome-capture sequencing with NGS. I am wondering if
there is a tool to identify SNPs on Galaxy? I would like to get SNP
information (position and allele frequency ) for each gene. Any
information is highly appreciated! Thanks!
Best wishes,
Yan
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Jennifer Hillman-Jackson
http://galaxyproject.org
___________________________________________________________
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
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