STR data for AmpF/STR Profiler Plus loci in south Poland

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Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
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Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

P Wolañska-Nowak1, W Branicki, T Kupiec

  • 1Institute of Forensic Research in Cracow, Forensic Haemogenetics Section, Westerplatte St. 9, 31-33 Cracow, Poland. pwolansk@ies.krakow.pl

Forensic Science International
|October 24, 2001
PubMed

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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...