Evidence map›Paper›PMID 20354713›Full record

ArticleInternational journal of legal medicine2010

X-linked insertion/deletion polymorphisms: forensic applications of a 33-markers panel.

Natalle S C Freitas, Rafael L Resque, Elzemar M Ribeiro-Rodrigues, João F Guerreiro, Ney P C Santos, Andrea Ribeiro-dos-Santos, Sidney Santos

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Article in International journal of legal medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

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  12. X-chromosomal 21-indel marker panel in German and Baltic populations.International journal of legal medicine · 2016
    Article
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  18. Automated Genotyping of a Highly Informative Panel of 40 Short Insertion-Deletion Polymorphisms Resolved in Polyacrylamide Gels for Forensic Identification and Kinship Analysis.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2012
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Natalle S C FreitasLaboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Cidade Universitária Prof. José da Silva Netto. Av. Augusto Corrêa, 01, Belém, PA, Brazil.
Rafael L Resque
Elzemar M Ribeiro-Rodrigues
João F Guerreiro
Ney P C Santos
Andrea Ribeiro-dos-Santos
Sidney Santos

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insertion/deletion (INDEL) polymorphisms are diallelic markers with potential characteristics for use in forensics and biological anthropology, including: the simplicity of laboratory analysis, the possibility of genotyping many markers in a single PCR multiplex reaction, as well as analyzing markers with special inheritance types, such as those linked to the X chromosome (X-INDEL). In this work we developed a laboratory analysis methodology using a 33-INDEL marker panel for the X chromosome in a single PCR multiplex reaction, followed by a capillary electrophoresis run. We employed the panel to genotype a sample of 351 individuals of a mixed population from the Brazilian Amazon. The results demonstrate that the measurement of biostatistical parameters for forensic use in this population is compatible with prior estimates from other populations using current X-STR panels.

Indexed as

PaternityBrazilChromosome MappingChromosomes, Human, XFemaleForensic GeneticsGene FrequencyGenes, X-LinkedGenetic MarkersGenetics, PopulationGenotypeHumansINDEL MutationLinkage DisequilibriumMalePolymorphism, GeneticGenetic Markers

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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.