Medical Sequencing Data: Difference between revisions
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== Mock Up of Genotype/Phenotype Track == | == Mock Up of Genotype/Phenotype Track == | ||
[[image:GenPhenTrack.gif]] |
Revision as of 20:24, 28 April 2006
Medical Sequencing Data
Some combination of phenotype and genotype ... Details unknown. Worthwhile to design ?
Major Types of information
- Subjects
- Anonymous individuals
- Family history
- Age
- Sex
- Ethnicity
- Pools of people
- Anonymous individuals
- Environmental data
- Location (zip code would be great)
- Medications they are taking
- Exercise, nutrition ...
- Genotype info
- Microarray based
- SNPs
- Haplotype blocks
- Copy number polymorphism
- Sequence based
- Random reads
- PCR products
- larger clones
- single haplotype vs. diploid
- Microarray based
- Phenotype
- Disease presence/absence or severity
- ADR - Adverse Drug Reaction
- Single physiological measure
- Enzyme activity, measure of amount of substance
- Parallel Measures
- Microarray measurements, etc...
Some Other Database Entities
- GenotypeTest - records what regions of genome probed.
- Study
- External URL
- Publications
- Contacts
- A group of subjects
- A set of phenotype and genotype tests
Existing Genotype/Phenotype Web Databases
http://www.pharmgkb.org/ - Requires registration for much data. Fan & Jim registered
http://globin.bx.psu.edu/genphen/ - Belinda, Ross and Webb's work, mostly covers hemoglobins
Mock Up of Phenotype Sorter
The Phenotype Sorter would be a web-based application aimed at presenting the full details of phenotype and genotype. The sorter has a line for each individual, and a column for each phenotype assayed in a study, and also a column for each genomic locus assayed in a study. The rows are sorted according the value of a selected phenotype, phe3 in the image above. The genotype columns are divided into a subcolumn for each allele, and at least for the simple nucleotide polymorphisms the alleles are labeled with the associated nucleotide. The number in the second row of the genotype label represents the strength of the locus as a marker for the phenotype. Possibly when sorting the rows by phenotype we should also sort the columns based on this number, though I was thinking of sorting the genotype columns just by position in genome initially.