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Whole Genome Sequencing
By: Qadardana kakar
BS Biotechnology
7th semester
Aims/Objective
 The aim of my presentation is to elucidate the Whole Genome Sequencing
technique and its protocol.
Discovery
 Sanger and his colleagues invented chain termination sequencing technique in 1970.
 Fragments of 100-1000 base pair.
 In 1979 shotgun sequencing technique was developed.
 Large size fragments.
 Overlapping of discovered fragments to detect whole genome sequences.
WGS Whole Genome Shotgun Sequencing
 To sequence all genome of a particular organism.
1. Find sequence.
2. Find their position in entire genome.
steps
 Collect and isolate the DNA or genome.
 Break into small manageable pieces.
 Copy each piece many times.
 Read the DNA sequence
 Assemble the data into a genome.
WGS
1. Different techniques are used to cut DNA into particular size pieces.
 Fragments are electrophoresed through gel to find the size of fragments.
2. Ligation of fragment into a plasmid.
4. Insert plasmid into bacteria e.g. E.coli.
Bacteria with plasmid select Transformed bacteria (incubated)
 5. Microtiter plate containing E.coli is heated to 95 degree Celsius.
 plasmids are released.
 6. PCR reaction amplify the plasmid.
Rolling circle amplification
 7. Desired sequence amplification (Stephenson, 2003).
8. DNA attracted toward the carboxyl coated magnetic bead.
 In Strong ethanol solution the carboxyl coat attracts the phosphate backbone.
 Cellular debris and reagents remain in solution.
 Wash with ethanol. Water added to each well.
 Water causes DNA to be released.
9.Sanger sequencing.
 10. Assembly
 Multiple read of the same genome is made.
 Reassembles by matching overlaps.
All Pictures are retrieved from: Whole genome sequencing/ YouTube.
Whole Genome Sequencing
Advantages
 To find coding non and non coding regions.
 Personalized drugs.
 Disease susceptibility prediction.
 Specie comparison and evolutionary studies.

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Whole genome sequencing

  • 1. Whole Genome Sequencing By: Qadardana kakar BS Biotechnology 7th semester
  • 2. Aims/Objective  The aim of my presentation is to elucidate the Whole Genome Sequencing technique and its protocol.
  • 3. Discovery  Sanger and his colleagues invented chain termination sequencing technique in 1970.  Fragments of 100-1000 base pair.  In 1979 shotgun sequencing technique was developed.  Large size fragments.  Overlapping of discovered fragments to detect whole genome sequences.
  • 4. WGS Whole Genome Shotgun Sequencing  To sequence all genome of a particular organism. 1. Find sequence. 2. Find their position in entire genome. steps  Collect and isolate the DNA or genome.  Break into small manageable pieces.  Copy each piece many times.  Read the DNA sequence  Assemble the data into a genome.
  • 5. WGS 1. Different techniques are used to cut DNA into particular size pieces.  Fragments are electrophoresed through gel to find the size of fragments. 2. Ligation of fragment into a plasmid.
  • 6. 4. Insert plasmid into bacteria e.g. E.coli. Bacteria with plasmid select Transformed bacteria (incubated)
  • 7.  5. Microtiter plate containing E.coli is heated to 95 degree Celsius.  plasmids are released.  6. PCR reaction amplify the plasmid. Rolling circle amplification
  • 8.  7. Desired sequence amplification (Stephenson, 2003).
  • 9. 8. DNA attracted toward the carboxyl coated magnetic bead.  In Strong ethanol solution the carboxyl coat attracts the phosphate backbone.  Cellular debris and reagents remain in solution.  Wash with ethanol. Water added to each well.  Water causes DNA to be released.
  • 10. 9.Sanger sequencing.  10. Assembly  Multiple read of the same genome is made.  Reassembles by matching overlaps.
  • 11. All Pictures are retrieved from: Whole genome sequencing/ YouTube.
  • 12. Whole Genome Sequencing Advantages  To find coding non and non coding regions.  Personalized drugs.  Disease susceptibility prediction.  Specie comparison and evolutionary studies.