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Introducción a la Bioinformática ,[object Object],[object Object],[object Object],[object Object]
What is Bioinformatics?
Introduction  ,[object Object],[object Object]
What is Bioinformatics?  ,[object Object]
What is Bioinformatics?  ,[object Object],[object Object]
Bioinformatics ,[object Object]
Bioinformatics ,[object Object],[object Object]
GOALS ,[object Object]
GOALS ,[object Object]
 
APPLICATIONS ,[object Object],[object Object],[object Object],[object Object]
APPLICATIONS ,[object Object],[object Object],[object Object]
APPLICATIONS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
APPLICATIONS ,[object Object]
APPLICATIONS ,[object Object]
APPLICATIONS ,[object Object]
Single-nucleotide polymorphism ( SNP ) ,[object Object],[object Object],[object Object],[object Object]
SNP and Human Disease ,[object Object],[object Object],[object Object]
SNP and Human Disease ,[object Object],[object Object],[object Object]
Cystic Fibrosis ,[object Object],[object Object],[object Object]
APPLICATIONS ,[object Object]
LIMITATIONS ,[object Object],[object Object]
LIMITATIONS ,[object Object]
NEW THEMES ,[object Object],[object Object]
Databases DNA Sequence Data EBI: http://www.ebi.ac.uk/ NCBI:http://www.ncbi.nlm.nih.gov/ DDBJ:http://www.ddbj.nig.ac.jp / (Sequence Retrieval System)  NCBI ( National Center for Biotechnology Information) ( European Bioinformatics Institute)
Introduction ,[object Object],[object Object],[object Object],[object Object]
WHAT IS A DATABASE? ,[object Object],[object Object],[object Object],[object Object]
Which courses are students from Texas taking?
[object Object]
MODERN DNA SEQUENCING
Historically there are two main methods of DNA sequencing: Maxam & Gilbert , using chemical  sequencing Sanger , using  dideoxynucleotides .   Modern sequencing equipment uses the principles of the Sanger technique.
How to obtain sequences
Step 1- Before submission for sequencing DNA purity & concentration is checked with the  ‘ Nanodrop ’
A Nanodrop readout of known concentration to be run as a control
Step 2 -Samples are received  and stored in the refrigerator and a request filed
Cost?
Samples arrive in Eppendorf tubes
Step 3 - paperwork. Each request is assigned a  ‘ well ’  in the sample tray and volumes of primers, water, dye, etc are calculated. A typical  ‘ run ’  has samples from a number of researchers
Step 4- Samples are agitated then centrifuged in an Ultracentrifuge to be sure they are in the bottom of their Eppendorf  tubes.
Step 5 - Reagents ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Micropipettors come in a range of sizes. They have disposable tips that hold tiny amounts of required reagents.
Step 6 - Preparing the wells ,[object Object],[object Object],[object Object]
Sample tray and micropipettor. Each tray holds 96 samples
Step 7 - The samples are run through a cycle sequencing process to get the fluorescent dyes incorporated by the DNA. The DNA and reagents are alternately heated and cooled over a 2 1/2 hour period.
A Sequence print-out from a control sample
THANK YOU

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Introducción a la bioinformatica

  • 1.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.  
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25. Databases DNA Sequence Data EBI: http://www.ebi.ac.uk/ NCBI:http://www.ncbi.nlm.nih.gov/ DDBJ:http://www.ddbj.nig.ac.jp / (Sequence Retrieval System) NCBI ( National Center for Biotechnology Information) ( European Bioinformatics Institute)
  • 26.
  • 27.
  • 28. Which courses are students from Texas taking?
  • 29.
  • 31. Historically there are two main methods of DNA sequencing: Maxam & Gilbert , using chemical sequencing Sanger , using dideoxynucleotides . Modern sequencing equipment uses the principles of the Sanger technique.
  • 32. How to obtain sequences
  • 33. Step 1- Before submission for sequencing DNA purity & concentration is checked with the ‘ Nanodrop ’
  • 34. A Nanodrop readout of known concentration to be run as a control
  • 35. Step 2 -Samples are received and stored in the refrigerator and a request filed
  • 36. Cost?
  • 37. Samples arrive in Eppendorf tubes
  • 38. Step 3 - paperwork. Each request is assigned a ‘ well ’ in the sample tray and volumes of primers, water, dye, etc are calculated. A typical ‘ run ’ has samples from a number of researchers
  • 39. Step 4- Samples are agitated then centrifuged in an Ultracentrifuge to be sure they are in the bottom of their Eppendorf tubes.
  • 40.
  • 41. Micropipettors come in a range of sizes. They have disposable tips that hold tiny amounts of required reagents.
  • 42.
  • 43. Sample tray and micropipettor. Each tray holds 96 samples
  • 44. Step 7 - The samples are run through a cycle sequencing process to get the fluorescent dyes incorporated by the DNA. The DNA and reagents are alternately heated and cooled over a 2 1/2 hour period.
  • 45. A Sequence print-out from a control sample