Who should register?
You don't need to register to access the database
Only those who wish to submit details of novel mutations or
who wish to submit details of people affected with ALS or wish to access the GWAS data need register. We are not
trying to restrict membership; we are trying to let you know whether you
to register. Most of the database may be accessed without restriction,
and registration is only necessary for submitting data
If you cannot answer YES to BOTH questions below, you do not need to register.
Do you have (or are likely to find) novel ALS related mutations AND/OR details
of people affected with ALS? AND Are you willing to submit data to
OR do you want to view GWAS data available on alsod? This has been passworded to avoid subject identification according to the publication:
Homer N, Szelinger S, Redman M, Duggan D, Tembe W, Muehling J, Pearson JV, Stephan DA, Nelson SF, Craig DW. Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays. PLoS Genet. 2008;4:e1000167. doi: 10.1371/journal.pgen.1000167 Abstract