1.1.3 Review Flashcards
Bioinformatics
The field of science to store and analyze genetic data
Outbreak
A sudden rise in the incidence of a disease
Genome
Complete set of DNA in a cell
Pathogen
A specific causative agent of a disease
Overall goal of 1.1.3
To identify the exact pathogen, we first need a sample of the patient’s lymph fluid. This fluid will contain the patients cells in addition to pathogen cells. From there, we need to isolate the DNA via DNA extraction. From there, will use PCR to amplify pathogen DNA. Then we run another PCR using fluorescently tagged Nucleotides in normal nucleotides to begin the DNA sequencing process. This will produce a set of DNA fragments that differ from a single base. From there, we will use electrophoresis in an automatic sequencer to generate a chromatogram that can then be read to obtain the pathogen sequence. after the sequence is obtain, the species can be identified by using bioinformatics by uploading the sequence into a molecular database.
What method was used in the video
Cycle sequencing
How long does it take to read an entire genome using this method
A few hours
What does it mean to read the Genome
Reading the genome means analyzing the specific nucleotide sequence
What is the role of a thermocycler
This is the machine that’s able to raise and lower the temperatures needed for each stage of PCR
What kinds of fragments are produced during this process
Fragments that differ in length by a single base
What is done to the fragments next
They are sorted by size
What is the top stand called
Template
Bottom strand
Complementary
 what strand is used for the rest of the sequencing process
Complementary
Primers
Short DNA fragments that buy specifically to target DNA.  They are starting points that allow DNA polymerase to begin replication