(Difference between revisions)
Revision as of 22:27, 2 April 2007
- Project Goal: Development of tools to aid in analysis of personal DNA sequences.
We would like to develop software and documentation that will help people get from sequence to diagnosis. At the moment, we are focusing on identifying and classifying SNPs, but we will broaden this identification to other things like large deletions or insertions or repeats when we have more expertise. We are attempting to harness the power of other already existing tools, and we would also like to make this tool one that others can build upon. Specifically, our program will eventually be able to determine location based on BLAST, determine any SNPs based on NCBI SNP, and give a prognosis based on OMIM and online medical databases.
- ATTENTION: Everyone needs to post their code to one place. Let's say everyone post a link from here that works to their code and then I'll be able to combine it all. --Katie Fifer
- Could someone who typed this up today please add the other sections that are being worked on? --TChan, 12:47 20 March 2007
- The following is from the information that Zach typed up in class (Located here) --Hetmann,
5:32 20 March 2007
- Editted to add some of my own notes and to reflect some semblance of order.. --Cchi 10:00, 22 March 2007 (EDT)
- PM / encourage documentation
Sequence to BLAST SNP to rs#
Accessing BLAST SNP using URLAPI
Info from BioPython (via Zach)
- It looks like that if you know the name of the database (here "snp/human_9606/human_9606"), then you can run for example
from Bio.Blast import NCBIWWW result_handle = NCBIWWW.qblast("blastn", "snp/human_9606/human_9606", seq) and then parse the results as usual (see section 3.4 in the Biopython tutorial).
--smd 18:05, 22 March 2007 (EDT)
OMIM XML Parse
- Xiaodi - completed? Yup: here
- rs -> OMIM XML parse -> phenotype text
- Resmi, Cynthia, and Hetmann
- Handling the text from the parse
Controlled Vocabulary for parsing OMIM records
- Masseroli et al.: "Our efforts to derive from the OMIM entries a controlled vocabulary of phenotype locations and descriptions enabled us to normalize and structure the valuable OMIM phenotypic data according to the obtained vocabulary and make them suitable for computational use. Although detailed phenotype descriptions could be further homogenized and standardized, their subdivision in hierarchical levels of detail that we performed allows to group specific phenotypes according to their common general traits, without loosing their specific characteristics. So, for example "Mental retardation, moderate" and "Mental retardation, nonspecific" can be both generally considered as "Mental retardation" and at the same time they can be treated as different types of mental defects. This provides the chance to modulate analysis granularity when searching for phenotypic traits shared among multiple diseases or genotypes. It also ensures more significant and clear results when categorical statistical analyses are performed at lower granularity levels of detail. Such interesting feature, proper of the hierarchical structure and hence belonging also to the defined phenotype location hierarchy, is exploited in the new GFINDer Genetic Disorders modules implemented for the study of genetic disorder related genes."
—smd 13:19, 22 March 2007 (EDT)
- Tiffany, Resmi, Deniz, Xiaodi, Mike, Chris (note: ask if API exists)
- Wikipedia (Mike) http://meta.wikimedia.org/wiki/API
- Webmd (Tiff)
- Emedicine (Resmi)
- Google, Medstory. (Deniz)
- Linking out of XML (Xiaodi)
- MedStory (Mike?)
- Pubmed (Chris)
- Downloading OMIM, extra functionalities, Eutils (Deniz)
- Chris, Deniz
- figure out with of multiple SNPs are relevant
- not in SNP db... then what? - I'd like to point out new efforts that aim to replace OMIM, called the "Human Variome Project" -- Deniz
- OMIM DOA
- systematically nonsyn. -> mutation not in OMIM or dbSNP?
- other dbs: genecard (spec. conservation, pop. freq)
- looking into linking gene expression w/ GEO?
Project ideas have been moved to their own page