What data is provided by the resequencing service?
We have a defined set of output data that will be provided to RS&G Service investigators at the completion of a project. The output includes the sequence files in FASTA format for the regions sequenced, the genotype and frequency of each allele for each SNP/variant and insertion-deletion polymorphism detected according to position mapping in the human genome, mapping of these SNPs/variants in the context of gene structure, and if requested, input files for programs like PHASEII Haploview and PLINK. These data files are provided as plain text and, as appropriate, may be imported into programs like Microsoft Excel for further analysis.
