Use this form if you are NOT using a Washington University email address. For WUSTL clients, use this form. First: (to fool spam robots), type the word "genotype" into this field : *required Ask questions and/or send us information about your genotyping project with this form. The GTcore home page lists costs and details for sample preparation, SNP selection, and Sequenom genotyping.

Please fill in the fields: Your name: *required Your email: *valid wustl.edu address required Department: *required P.I. for your Lab: *required Lab phone: *required Question or Comment: *** Before sending, please enter information in the fields listed below IF you have a good idea of what you want genotyped ***

SAMPLE INFORMATION Approximate number of DNA samples: Species (if not human): Approx. date you expect to have DNA ready to genotype: Do you want us to determine sample concentrations (DNA quantification) for you? NO YES MARKER INFORMATION Approximate number of SNPs: You may email files of SNP names/sequences directly to cindy at hg.wustl.edu, or list the known SNPs here. Your rs-numbered SNP list: ** OR ** if you want us to choose validated rs-numbered SNPs for you (at additional labor cost), fill in the pink section below Fill in either section 1 (by genomic region) or section 2 (by gene): Genomic region(s) If you want to define a region by rsSNP IDs: enter the two boundary SNPs here: Else give genomic region(s) to be covered (e.g., chr7:101000111-101111110): (build ) (genomic build that applies to that chromosome position, e.g., hg17 build 35, or hg18 build 36) Gene(s) to be covered. Please use gene symbols as listed at UCSC or NCBI. Include the chromosome and/or position if you know it. If you want to change default upstream/downstream included region (10,000 bp), enter bp to be included upstream: bp downstream: bp We find SNPs using two methods, tag and block. TAGGER r2 usually covers a region with fewer SNPs than the Haploview blocks method. Choose which method you prefer. You will receive the results by email. TAG SNPs (we use Hapmap genotypes and TAGGER r2 pairwise to find TAG snps) BLOCK SNPs (uses Hapmap genotypes with Haploview GABRIEL method to find SNPs defining all haplotypes in each block. The result includes all inter-block SNPs. CHECK which HAPMAP population to use (default is CEPH) CEPH: Ancestry from northern and western Europe YRI: Yoruba in Ibadan, Nigeria JPT: Japanese in Tokyo, Japan CHB: Han Chinese in Beijing, China Your include SNP list, if any: Your exclude SNP list, if any: You may email files of SNP names/sequences directly to cindy at hg.wustl.edu

Notes about SNP designs: