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Paternity Lab Report

The document outlines the 5 main steps involved in processing DNA samples for paternity testing: 1. Collection of samples through blood tests or cheek swabs from the alleged father and child. 2. Extracting the DNA from the samples through lysis to break open the cells and retrieve the DNA. 3. Separating and purifying the DNA through precipitation, alcohol washing, and electrophoresis. 4. Genotyping the DNA using PCR to copy specific DNA sequences for analysis. 5. Testing the copies for genetic markers and comparing markers between the child and alleged father to determine paternity through a DNA report and probability percentage.

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0% found this document useful (0 votes)
176 views5 pages

Paternity Lab Report

The document outlines the 5 main steps involved in processing DNA samples for paternity testing: 1. Collection of samples through blood tests or cheek swabs from the alleged father and child. 2. Extracting the DNA from the samples through lysis to break open the cells and retrieve the DNA. 3. Separating and purifying the DNA through precipitation, alcohol washing, and electrophoresis. 4. Genotyping the DNA using PCR to copy specific DNA sequences for analysis. 5. Testing the copies for genetic markers and comparing markers between the child and alleged father to determine paternity through a DNA report and probability percentage.

Uploaded by

Eniola Johnson
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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MDSC/DENTC1104: Introduction Molecular Medicine

DNA/ Paternity Lab


Due Tuesday October 18 at 1pm.
Collection Venue: Outside of Lecture Theatre 3
PART A

1. What are the steps involved in processing DNA samples to determine paternity?
NB. Please provide detailed explanation of each step (35 marks)

STEPS INVOLVED IN PROCESSING DNA SAMPLES FOR PATERNITY


Introduction:
DNA is the genetic material that needs to be tested. It can be tested for several things. It can

be used to identify genetic mutations. DNA may also be used to assist in criminal

investigations. Additionally, it is used to establish a value for a child's paternity. Paternity

tests can be very accurate almost 100%. It is done using something known as an STR test.

STR stands for short tandem repeats. These repeats found on the gene are the basis used for

paternity testing.

Step 1: Collection of the sample

This could be done in two ways, blood tests or a less invasive cheek swab. The

father and child will be in a medical facility and must consent to take the blood test or

swab. The blood may be taken from the arms of the family. The swab is taken from

the cheeks of the patients by the patients or a licensed practitioner. One swab must be

done for each cheek and each should last approximately 30 seconds.

Step 2: Extracting the DNA


The extraction of the DNA will differ based on the sample, whether blood or

tissue. The cells must be lysed to obtain their internal contents. Lyse comes from the

word lysis which means to disintegrate. Lysing is a process by which the cell is

broken open and the DNA within is retrieved. It may be done thermally, chemically,

or even with the use of enzymes for example Proteinase K.

PCR amplification of multiple STR loci simultaneously, or multiplexing utilizes

different coloured flurescent dyes

Step 3: Separating DNA

The DNA obtained may be contaminated or mixed around with debris and

chemicals that may have been used in the previous step. It must be isolated and

purified. DNA is then precipitated using sodium ions which will make the molecules

less water soluble and help with stability. Alcohol is added and causes the DNA to

precipitate out of the aqueous solution because it isn’t soluble in alcohol. Adding a

protease will degrade any DNA-associated proteins. Purification is the next step. The

DNA is rinsed with alcohol, specifically isopropanol or absolute ethanol, removing

the rest of the unwanted debris. Then it is dissolved in water for proper storage. The

most popular method of separation though is electrophoresis because DNA is

negatively charged. This uses an electric field to move molecules through a gel-like

substance or matrix. They migrate to the positive electrode and as smaller fragments

move faster; the larger ones move slower. They are arranged in order of size and the

bands formed are compared throughout the family.

Step 4: Genotyping using PCR


After separation, the DNA is copied using the PCR technique.

PCR is a process that produces millions of copies of a selected DNA sequence. DNA

polymerases and 2 primers are needed as well as large amounts of the 4 DNA

nucleotides. The primers are needed as a starting point for the new strand so the DNA

polymerase can go to work. The DNA that has been stored is then heated to separate

the double strand into single strands. It is cooled and the primers begin to bind to their

complement sequences. This is done to give a small segment of the DNA that is

desired. It’s then heated once more as the polymerases build new strands of the DNA

by attaching the nucleotides until the segment is filled. Now you have the specific

copied sequence needed for the study.

Step 5: Testing

These copies are Tested for genetic markers. Loci which are the locations of

these markers house two alleles that are from each parent. A comparison must be

made to the population database based on the phenotype the individual displays. After

the known genetic markers are located, they are compared and matched between the

child and parent/s. A paternity report is prepared.

2. What is a paternity report and how is it analyzed? (10 marks)

A paternity report is a DNA test utilized to determine the relationship between

a mother, an alleged father and their child. In this report, you will see columns

showing the loci, alleles, respective paternity index, as well as combined paternity

index and probability of paternity. A paternity index is a numerical tool used to see

how similar each selected locus is.


The combined Paternity Index is the number on the report that encompasses a ratio

that shows how likely it is that the alleged father is the biological father. The CPI can

range from 0 to infinity. The higher the CPI is the more likely the alleged father is

biological. Next, you will have the paternity percentage. In conclusion, the document

may state “is excluded/not excluded as the biological father” Is excluded ultimately

means the father is not biological.

PART B

3. Please complete the table below with the data from cases A & B.

CASE 1: PATERNITY TABLE FOR ALLEGED FATHER AND CHILD ONLY


Locus Child Alleged Shared Frequency Formula Paternity
Father Allele of Allele Index (PI)
CSF1PO 7,10 7 7 0.04286 1/2q 11.666
D5S818 8,12 8,13 8 0.05 1/4q 5.000
D7S820 9,10 9,10 9,10 0.15714, (p+q)/4pq 2.363
0.32381
TPOX 11 11 11 0.22488 1/q 4.447
D18S51 16,19 16,21 16 0.18889 1/4q 1.324

CASE 2: PATERNITY TABLE FOR ALLEGED FATHER AND CHILD ONLY


Locus Child Alleged Shared Frequency Formula Paternity
Father Allele of Allele Index
D21S11 31, 33.2 31, 35 31 0.09218 1/4q 2.712
D5S818 13 15 None 1 0 0.000
THO1 6, 8 6, 9 6 0.10952 1/4q 2.283
Vwa 16 18,20 None 1 0 0.000
D18S51 13,18 16,20 None 1 0 0.000

(40 marks)

4. Determine the PI, combined PI and the probability of paternity for cases A&B.
(30 marks)
Combined PI= Product of all the PIs of the loci used

CPI for A =11.666 x 5.000 x 2.363 x 4.447 x 1.324


CPI for A = 811.542

Probability of paternity:
(CPI x 0.5)/ [(CPI x 0.5) +0.5] x 100
811.542 x 0.5)/ [(811.542 x 0.5) + 0.5] x 100
= 99.88%

CPI for B = 2.712 x 0.000 x 2.283 x 0.000 x 0.000


CPI for B= 0

Probability of paternity
0%
References (APA format) (5 marks)

Endeavor DNA. (2021, September 1). What is the process for DNA testing? Endeavor DNA.
Retrieved October 16, 2022, from https://endeavordna.com/blog/process-dna-test/

Total marks: 120

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