Evidence Analysis, Recovery and QA Flashcards

(32 cards)

1
Q

When may DNA samples be rejected?

A

If they are non-compliant

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2
Q

What does PPE protect?

A

Staff and exhibits

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3
Q

How are exhibits separated?

A

By time and space

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4
Q

What is paramount in a lab?

A

Cleanliness

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5
Q

How is packaging opened?

A

In a way that protects the seals as much as possible

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6
Q

How are details of an exhibit recored?

A

On a worksheet

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7
Q

What is the point of examination?

A

To identify points of interest

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8
Q

What can go wrong in a lab? (6)

A

Staff, equipment, tests, procedures, integrity and delivery

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9
Q

How often is a method tested for quality control?

A

Constantly

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10
Q

What about samples is argued in court?

A

Integrity

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11
Q

How many cells are required for a DNA profile?

A

At least 3

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12
Q

How are results interpreted?

A

Based on guidelines

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13
Q

What happens when something goes wrong?

A

Corrective action is taken

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14
Q

What ensures standards are met?

A

Accreditation

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15
Q

What is removed in DNA extraction?

A

Interfering proteins and enzymes

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16
Q

What are the two DNA extraction steps?

A

Breaking the matrix and lysing the cells

17
Q

How is a DNA matrix broken? (2)

A

Mechanical (Mortar and pesel) or Chemical (Protein Kinase A)

18
Q

What is the difference between organic extraction, silica kits and Chelex?

A

Organic extraction is more pure but takes longer than Chelex. Silica kits are in between.

19
Q

What is the most widely used form of DNA extraction?

20
Q

Why is Chelex advantageous for PCR?

A

Because it removes inhibitors

21
Q

What is quality assurance?

A

The planned, systematic practise to provide confidence in a product

22
Q

What is quality control?

A

The scrutiny of daily techniques

23
Q

Why are audits conducted?

A

To make sure standards are met

24
Q

What do positive and negative tests ensure?

A

Reagents are working properly

25
What is validations purpose?
To show that techniques are robust
26
What provides interpretation guidelines?
Standard Operating Procedures
27
What does too much DNA result in?
Overblown electropherograms
28
What does too little DNA result in?
A loss of alleles
29
How many PCR cycles does it take to have 1 billion copies of DNA?
32
30
How large is a PCR assay?
5-100uL
31
What does a negative control test for?
Contamination
32
Why is contamination an issue with PCR?
Due to how sensitive the method is, it can detect very small amounts of DNA.