Evidence map›Paper›PMID 26164591›Full record

ArticleInternational journal of legal medicine2016

X-chromosomal 21-indel marker panel in German and Baltic populations.

Jeanett Edelmann, Michael Kohl, Jan Dressler, Andre Hoffmann

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Article in International journal of legal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jeanett EdelmannInstitute of Legal Medicine, University of Leipzig, Leipzig, Germany. jeanett.edelmann@medizin.uni-leipzig.de.
Michael KohlInstitute of Legal Medicine, University of Leipzig, Leipzig, Germany.
Jan DresslerInstitute of Legal Medicine, University of Leipzig, Leipzig, Germany.
Andre HoffmannInstitute of Legal Medicine, University of Leipzig, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to verify specific biallelic X-indels and their characteristic properties in distinct populations, one German and three Baltic population groups (Estonia, Latvia, and Lithuania) have been analyzed by a short amplicon method, which also enables detection of degraded DNA samples. To combine 21 indels in a single multiplex PCR, all products were arranged according to their expected amplicon length (~40-160 bp) on the basis of three different fluorochromes. Separation of PCR products was carried out in a single capillary electrophoresis. Data evaluating was performed including five further indel markers which have already been tested in identical samples, resulting in altogether 26 markers. The majority of the genetic material showed combinations of insertion elements (L-fragments). Combinations of deletion elements (S-fragments) in contrast occurred with significant lower ratios. Hardy-Weinberg equilibrium (HWE) was observed for all markers except for MID1361 and MID329. This was attributed to an insufficient number of samples. For two known linkage groups within the 26-indel set (MID357-MID356 and MID3690-MID3719-MID2089), haplotype data were determined. A pairwise comparison of German and Baltic allele frequencies did not show significant deviation. This result indicates a possible genetic association between all four population groups. The calculated biostatistical parameters show high forensic efficiency for this set of indel markers. In a segregation analysis investigating 194 meiosis, no mutations have been detected regarding expected transmission patterns.

Indexed as

Chromosomes, Human, XGenetic MarkersGenetics, PopulationINDEL MutationBaltic StatesElectrophoresis, CapillaryFemaleGene FrequencyGermanyHumansMaleMultiplex Polymerase Chain ReactionGenetic MarkersChromosome XForensic geneticsIndel polymorphism (indel)Population data

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.