ChroMoS
ChroMoS (Chromatin Modified SNPs) combines genetic and epigenetic data
to facilitate SNP classification, prioritization and prediction of their functional effect.
SNP Input Methods
ChroMoS Manual
Press corresponding radio button to enable preferable input method.
Manual entry of SNPs or file upload in VCF format. Press NEXT button.
GWAS SNPs
Enter validated dbSNP [build 137] rs# one per line. Press NEXT button.
SNP catalog of published genome-wide association studies (March 2013)
Enter Disease trait (e.g. Crohn's disease) or Pubmed id (e.g. 21102463):
Choose one PUBMED id. Press NEXT button.
Enter GWAS SNP id (e.g. rs3091315):
Choose one PUBMED id. Press NEXT button.
Bioinformatics and Next Generation Sequencing Group
;
Max Planck Institute of Immunobiology and Epigenetics
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