Republic of the Philippines CASE NO.

National Police Commission

Tanza Crime Laboratory DNA-TCCL-222-22
Tanza, Cavite
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RESULTS:

DNA profiles were obtained from the following specimen:

 Muscle tissue marked as UMC
 Blood Obtained from the shirt of the suspect
 Blood obtained from the victim

CONCLUSION:
The DNA profiles obtained from the specimens are came from the same person.
The probability of parentage for this case is 99.99%

REMARKS:
The remaining portions of the specimens and/or extracted DNA from this case are currently
being stored at the PNP DNA laboratory.

EXAMINED AND APPROVED BY:

VINCE L. AGUSTIN
Police Chief Inspector
Chief, DNA Analysis Branch
NOTED: ASSISTED BY:

FELIPE E. LUBIGAN JONATHAN TORDERA

Police Senior Superintendent Non-Uniformed Personnel
Acting Chief of Staff/R4 Forensic DNA Technical Asistant
 Republic of the Philippines CASE NO.
National Police Commission
Tanza Crime Laboratory DNA-TCCL-222-22
Tanza, Cavite
PAGE NO.

1 of 3
DNA LABORATORY REPORT
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NATURE OF THE CASE: TIME AND DATE RECEIVED:

Robbery with Homicide Incident 10:00 am August 6,2017

REQUESTING PARTY: TIME AND DATE COMPLETED:

OIC, SPDCLO 1:00 pm August 12, 2017

SUSPECT: VICTIM:
Crisanti Barron y Illarde Kimberly A. Moncada

SPECIMEN SUBMITTED:

SPECIMEN SOURCE SPECIMEN DESCRIPTION Remarks

CODE
310-17-A1041 Q Muscle tissue marked as UMC Examined

310-17-A1044 STD Blood from the shirt of the suspect Marked as FPC Examined

310-17-A1045 STF Blood from the Victim marked as TJC Examined

V= victim Q= questioned NE= not examined

S= suspect STD= standard sample ES= elimination sample
DNA TESTING METHODS AND GENERIC MARKERS:
The submitted piece of specimen were subjected to DNA extreaction, the DNA was amplified using
the polymerase chain reaction (PCR) and the powerplex fusion 6c, system provided by the
promega corporation, the generic marker tested include amel, D3S1358, D1S1656, D2S441,
D10S1248, Penta E, D16D549, D18S51, D2S1338, CSF1PO, Penta D, TH01, VWA, D21S11,
D7S820, TPOX, D8S1179, SE33, FGA the PCR fragments were separated and detected using an
applied biosystem 3500 HID generic analyzer, the data was analyzed using genemapper IDv1.4
software. the result of the analysis is presented in table 1.