Harvard:Biophysics 101/2007/Project: Difference between revisions

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* Deniz: [[Harvard:Biophysics_101/2007/Notebook:Denizkural/2007-4-3|examples of coding]] which returns news updates in several formats
* Deniz: [[Harvard:Biophysics_101/2007/Notebook:Denizkural/2007-4-3|examples of coding]] which returns news updates in several formats
* Tiff: [[TChan/Notebook/2007-5-2|code]] (a) displays relevant URLs (, (b) returns lists of drugs, clinical trials, experts, etc.
* Tiff: [[TChan/Notebook/2007-5-2|code]] (a) displays relevant URLs (, (b) returns lists of drugs, clinical trials, experts, etc.
* Tiff: [[TChan/Notebook/2007-5-3#Allelic_Frequency|code]] outputs allelic frequency data parsed from dbSNP (what we actually want to show to the user must be selected out of the data)
* Resmi: [[Harvard:Biophysics_101/2007/Notebook:Resmi_Charalel/2007-4-5|code]] displays PubMed review citations in text form
* Resmi: [[Harvard:Biophysics_101/2007/Notebook:Resmi_Charalel/2007-4-5|code]] displays PubMed review citations in text form
* Cynthia: [[Harvard:Biophysics_101/2007/Notebook:CChi/2007-4-24|code]] displays PubMed article citations in text form
* Cynthia: [[Harvard:Biophysics_101/2007/Notebook:CChi/2007-4-24|code]] displays PubMed article citations in text form

Revision as of 01:53, 3 May 2007

Biophysics 101: Genomics, Computing, and Economics

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Completed HTML Interface

Overview

  • Project Goal: To develop 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.

Inputs & Outputs

Path 1: Using BlastSNP

[1]. Sequence → RS Number (BLAST SNP)→ Disease Name (OMIM)

  • Xiaodi: code prints and outputs to file pickled version of the OMIM output for our sequence
  • Chris: quality checking code returns sequences back after dbSNP
  • Kay: Work-around for SNPs non-directly linked to OMIM

[2]. RS Number → PubMed Articles → Mesh Terms

  • Cynthia code (1) input: rs#, (2) output: list of mesh terms (3) prints top 5 PubMed articles, print list of mesh terms


[3]. RS Number (OMIM) → PubMed PMIDs → Mesh Terms

  • Resmi: code (1) parses OMIM XML to (2) get PubMed PMIDs to (3) get Mesh Terms


[4]. Mesh Terms → Disease Name (in-house code)

  • Deniz
  • Zach: code finds mesh codes(cynthia), determines most important mesh codes, finds prevalence, find CDC ID and formal disease name.b

[5]. Disease Name → Prevalence (→ regulates Useful Patient Info)

  • Zach: see above, complete and compiled

[6]. Disease Name → Useful Patient Info (Medical search engines)

  • Deniz: examples of coding which returns news updates in several formats
  • Tiff: code (a) displays relevant URLs (, (b) returns lists of drugs, clinical trials, experts, etc.
  • Tiff: code outputs allelic frequency data parsed from dbSNP (what we actually want to show to the user must be selected out of the data)
  • Resmi: code displays PubMed review citations in text form
  • Cynthia: code displays PubMed article citations in text form

[7]. All displayable data → Web Interface

  • Xiaodi and Katie: code and description displays (some - still need to integrate some remaining scripts) preceding data in a web interface

Path 2: Using GenBank and PolyPhen

[1]. Sequence → Gene Name (BLAST)

  • Zach code returns through BLAST HTML parse if is in CDS or not, and for former the CDS , asc#, and seq, and for latter the seq. info and surrounding genes
  • Katie code returns BLAST XML data.

[2]. Gene Name → Mutations (GenBank)

  • Xiaodi
  • Chris: quality checking code detects mismatches between our sequence and returned SNPs


[3]. Gene Name → ??? (PolyPhen)

  • Mike


[4]. Mutations → Disease Name (OMIM)

  • Xiaodi


[5]. Disease Name → Useful Patient Info (Medical search engines)

  • Deniz:
    • examples of code which returns Google news updates and MedStory news updates in several formats
    • blogs through technorati
    • clinical trials by disease name and by drug
    • medical articles and resources
    • research articles
  • Tiff: code (a) displays relevant URLs, (b) returns lists of drugs, clinical trials, experts, etc.
  • Resmi: code displays PubMed review citations in text form
  • Cynthia: code displays PubMed article citations in text form

[6]. All displayable data → Web Interface

  • Xiaodi and Katie: code and description displays (some - still need to integrate some remaining scripts) preceding data in a web interface
  • Deniz - write the output HTML for news, drugs, research articles, and all the other output.

Diagram

Project Diagram


Project-in-Progress

Project-in-Progress notes have been moved to their own page.

Project Ideas

Project ideas have been moved to their own page.