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FRNSC 421 - EXAM 3 PRACTICE QUESTIONS AND ANSWERS (100% PASS)

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  • FRNSC421W /FRNSC 420
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  • FRNSC421W /FRNSC 420

FRNSC 421 - EXAM 3 PRACTICE QUESTIONS AND ANSWERS (100% PASS) lineage markers - Answer️️ -useful for assisting with the identification of related individuals separated by generational events - Y DNA paternally inherited - mtDNA maternally inherited Thomas Jefferson case - Answer️️ -Y-S...

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  • August 31, 2024
  • 14
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • FRNSC421W /FRNSC 420
  • FRNSC421W /FRNSC 420
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©PREP4EXAMS2024/2025 REAL EXAMS DUMP Wednesday, August 7, 2024 9: 33 PM



FRNSC 421 - EXAM 3 PRACTICE QUESTIONS AND ANSWERS (100% PASS)



lineage markers - Answer✔️✔️-useful for assisting with the identification of related
individuals separated by generational events

- Y DNA paternally inherited

- mtDNA maternally inherited

Thomas Jefferson case - Answer✔️✔️-Y-STR analysis on descendent of Eston
Hemmings to determine if Thomas Jefferson had an affair with his slave Sally
Hemmings

- showed that Eston is related to the Jefferson family, cannot conclusively say it
was Thomas who fathered him

- Tom Woodson, Sally's eldest son, more closely related to Thomas Jefferson's
nephew

applications of Y-STR testing - Answer✔️✔️-- ID & historical cases to verify
relationships

- sexual assault evidence when autosomal STR data produces minor mixed male
profile

- verification of familial testing outcomes, identifying potential paternal relatives
of potential perpetrators

- paternity testing in motherless cases

Y chromosome structure - Answer✔️✔️-has lost ~97% of its genes over the last 300
million years, estimated to lose all genes within the next 10 million




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, ©PREP4EXAMS2024/2025 REAL EXAMS DUMP Wednesday, August 7, 2024 9: 33 PM


- has male-specific region (MSY) and synonymous non-recombining portion
(NRY)

- lowest gene but highest repetitive sequences/copy number variants

- sex-determining gene in Yp arm

Yfiler - Answer✔️✔️-tests for 16 loci and 17 alleles, including:

- european minimal haplotype loci (MHL) = 8 loci, 9 alleles

- SWGDAM 10 loci

- Yflier has 6 additional loci

- Yfiler Plus has 9 additional loci (10 alleles); 3 highly diverse single allele loci,
and 6 rapidly mutating loci including one multi-locus marker

PowerPlex Y23 - Answer✔️✔️-tests for 22 loci and 23 alleles

- only 2 rapidly mutating loci

DYS385 a/b - Answer✔️✔️-one of 10 SWGDAM loci

- duplicated a and b regions ~40 kb apart facing away from one another

- result of a translocation event duplicating/inverting the locus

- counted as a single locus, use same forward/reverse primers

- results in "heterozygote" profiles when a ≠ b; reported as such, but isn't classified
as such

DYS389 I/II - Answer✔️✔️-one of 10 SWGDAM loci

- I and II loci "on top of" one another

- same mutational event as DYS385a/b, except not inverted

- defined as two loci that are close together


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