Evidence map›Paper›PMID 30612323›Full record

ArticleInternational journal of legal medicine2019

Genetic characterization of 32 X-InDels in a population sample from São Paulo State (Brazil).

Juliana Martinez, Fernanda Silva Polverari, Flávia Alves de Jesus Silva, Danilo Faustino Braganholi, Joyce Aparecida Martins Lopes Ferraz, Leonor Gusmão, Regina Maria Barretto Cicarelli

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of legal medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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.

Juliana MartinezLaboratory of Paternity Investigation, School of Pharmaceutical Sciences, São Paulo State University (UNESP), São Paulo, Brazil. jumrtz@hotmail.com.ORCID http://orcid.org/0000-0003-3496-1961
Fernanda Silva PolverariLaboratory of Paternity Investigation, School of Pharmaceutical Sciences, São Paulo State University (UNESP), São Paulo, Brazil.
Flávia Alves de Jesus SilvaLaboratory of Paternity Investigation, School of Pharmaceutical Sciences, São Paulo State University (UNESP), São Paulo, Brazil.
Danilo Faustino BraganholiLaboratory of Paternity Investigation, School of Pharmaceutical Sciences, São Paulo State University (UNESP), São Paulo, Brazil.
Joyce Aparecida Martins Lopes FerrazResearch Centre for Biochemistry and Molecular Biology, Medical School of São José do Rio Preto (FAMERP), São Paulo, Brazil.
Leonor GusmãoDNA Diagnostic Laboratory (LDD), State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.
Regina Maria Barretto CicarelliLaboratory of Paternity Investigation, School of Pharmaceutical Sciences, São Paulo State University (UNESP), São Paulo, Brazil.

Funding

Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior No numberFunda??o de Amparo ? Pesquisa do Estado de S?o Paulo 16/10138-8
6 · The paper itself

Abstract

X-chromosomal markers can be useful in some forensic cases, where the analysis of the autosomal markers is not conclusive. In this study, a population sample of 500 unrelated individuals born in São Paulo State was characterized for 32 X-InDel markers. No deviations from the Hardy-Weinberg equilibrium were detected, except for MID1361. The 32 X-InDels showed an accumulated power of discrimination of 0.9999999999993 in females and 0.99999993 in males and an exclusion chance of 0.999996 in trios and 0.99995 in duos. São Paulo showed lower genetic distances to the Colombian admixed and European populations than to Native American, Asian, or African populations. Ancestry analysis revealed 41.8% European, 31.6% African, and 26.6% Native American contributions. Segregation analysis was performed in 101 trios, and the mutation rate was estimated to be low.

Indexed as

INDEL MutationAmerican Indian or Alaska NativeBlack PeopleBrazilChromosomes, Human, XFamilyFemaleGenetic MarkersGenetics, PopulationHaplotypesHumansMaleMultiplex Polymerase Chain ReactionMutation RatePaternityWhite PeopleGenetic MarkersForensic geneticsHuman identificationInsertion/deletion polymorphismKinship testingX chromosome

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.