Paternity testing.

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Paternity Testing

Paternity testing can be done by older methods including ABO blood group typing, analysis of various other proteins and enzymes, or using human leukocyte antigen (HLA). However, DNA testing became the only formal and exact method for the paternity testing now. For DNA testing of paternity determination, the DNA collection using an easily obtained cheek swab saliva sample. Fast, proprietary and ...

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Blood Group ABO Genotyping in Paternity Testing.

BACKGROUND: The ABO blood groups result from DNA sequence variations, predominantly single nucleotide and insertion/deletion polymorphisms (SNPs and indels), in the ABO gene encoding a glycosyltransferase. The ABO blood groups A(1), A(2), B and O predominantly result from the wild type allele A1 and the major gene variants that are characterized by four diallelic markers (261G>del, 802G>A, 803G...

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ISFG: Recommendations on biostatistics in paternity testing.

The Paternity Testing Commission (PTC) of the International Society for Forensic Genetics has taken up the task of establishing the biostatistical recommendations in accordance with the ISO 17025 standards and a previous set of ISFG recommendations specific to the genetic investigations in paternity cases. In the initial set, the PTC recommended that biostatistical evaluations of paternity are ...

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Paternity testing in case of brother-sister incest.

We performed a paternity test in a case of incest between brother and sister. DNA from blood samples of the alleged parents and their two children was obtained with Chelex DNA extraction method and quantified with Applied Biosystems QuantiBlot quantitation kit. Polymerase chain reaction (PCR) amplification of DNA samples was performed with AmpFlSTR SGM Plus PCR amplification kit and GenePrint P...

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Development of SNP microarray for supplementary paternity testing

We have developed a SNP microarray for paternity testing, which contains 10 SNPs and in addition X and Y chromosome-specific markers. SNPs were selected with an emphasis on their high allele frequency in the Finnish population. Coding regions of known genes were excluded. With this setup of SNPs, we have calculated the average exclusion power in paternity testing to be 86.5%. The array was vali...

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ژورنال

عنوان ژورنال: BMJ

سال: 1977

ISSN: 0959-8138,1468-5833

DOI: 10.1136/bmj.2.6085.520-c