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Thread | Thread Starter | Forum | Replies | Last Post |
Somatic Mutations in dbSNP | qqcandy | Bioinformatics | 14 | 07-27-2015 03:34 PM |
Detection of somatic mutations in normal & tumour paired NGS data | Jane M | Bioinformatics | 16 | 10-11-2013 10:49 AM |
Pipeline to find somatic mutations | david.tamborero | Bioinformatics | 6 | 08-09-2013 03:05 AM |
antisense transcripts for all genes in signalling pathway | niti217 | Bioinformatics | 2 | 03-14-2012 09:26 AM |
Samtools mpileup_Paired Tumoral / Germline_keep only somatic mutations | Sam64 | Genomic Resequencing | 2 | 02-29-2012 12:01 PM |
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#1 |
Member
Location: Seoul, South Korea Join Date: Oct 2011
Posts: 30
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Hi all
![]() I sequenced cancer exomes matched with normal exomes, then after alignment follwed by de-duplication, I extracted significant somatic mutations from the pile-up files with VarScan somatic option. I want to ask if any of you can recommend me some decent pathway analyses, with "stringGene & integerSomaticMutation" as experimental input. (Known pathways like KEGG or Reactome probably will be its database.) I saw many gene-set (not essentially pathways) enrichment analyses, with <phenotype of a sample>, <gene-expression-per-gene of a sample> as input (e.g. GSEA or Ingenuity), but I haven't yet found a nice automated tool that gives you several significant candidate pathways when <gene:somatic-mutations> are given as input, not <gene:expression level>. I think there are such tools out there; there is a high possibility I could not find them. Have a joyful day!! ![]() |
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Tags |
cancer exome, cancer genome, exome sequencing, pathway analysis, somatic mutation |
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