Evidence map›Paper›PMID 27090252›Full record

ArticleThe HUGO journal2014

A whole genome analyses of genetic variants in two Kelantan Malay individuals.

Wan Khairunnisa Wan Juhari, Nur Aida Md Tamrin, Mohd Hanif Ridzuan Mat Daud, Hatin Wan Isa, Nurfazreen Mohd Nasir, Sathiya Maran, Nur Shafawati Abdul Rajab, Khairul Bariah Ahmad Amin Noordin, Nik Norliza Nik Hassan, Rick Tearle and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The HUGO journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact, top 82% of its field
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

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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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

13 authors at 4 institutions in 2 countries.

Wan Khairunnisa Wan JuhariDepartment of Pediatrics, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia.
Nur Aida Md TamrinFaculty of Resource Science and, Technology Universiti Malaysia Sarawak, Sarawak, Malaysia.
Mohd Hanif Ridzuan Mat DaudFaculty of Resource Science and, Technology Universiti Malaysia Sarawak, Sarawak, Malaysia.
Hatin Wan IsaHuman Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Universiti Sains Malaysia, Kelantan, Malaysia.
Nurfazreen Mohd NasirHuman Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Universiti Sains Malaysia, Kelantan, Malaysia.
Sathiya MaranHuman Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Universiti Sains Malaysia, Kelantan, Malaysia.
Nur Shafawati Abdul RajabHuman Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Universiti Sains Malaysia, Kelantan, Malaysia.
Khairul Bariah Ahmad Amin NoordinSchool of Dental Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
Nik Norliza Nik HassanSchool of Health Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
Rick TearleComplete Genomics Inc, 2071 Stierlin Court, Mountain View, 94043, CA, USA.
Rozaimi RazaliSengenics Sdn Bhd, Kuala Lumpur, Malaysia.
Amir Feisal MericanCentre of Research for Computational Sciences and Informatics in Biology, Bioindustry, Environment, Agriculture and Healthcare (CRYSTAL), Kuala Lumpur, Malaysia.
Bin Alwi ZilfalilDepartment of Pediatrics, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia. zilfalil2@hotmail.com.
Universiti Sains Malaysia · MYUniversiti Malaysia Sarawak · MYComplete Genomics (United States) · USUniversity of Malaya · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe sequencing of two members of the Royal Kelantan Malay family genomes will provide insights on the Kelantan Malay whole genome sequences. The two Kelantan Malay genomes were analyzed for the SNP markers associated with thalassemia and Helicobacter pylori infection. Helicobacter pylori infection was reported to be low prevalence in the north-east as compared to the west coast of the Peninsular Malaysia and beta-thalassemia was known to be one of the most common inherited and genetic disorder in Malaysia.

resultBy combining SNP information from literatures, GWAS study and NCBI ClinVar, 18 unique SNPs were selected for further analysis. From these 18 SNPs, 10 SNPs came from previous study of Helicobacter pylori infection among Malay patients, 6 SNPs were from NCBI ClinVar and 2 SNPs from GWAS studies. The analysis reveals that both Royal Kelantan Malay genomes shared all the 10 SNPs identified by Maran (Single Nucleotide Polymorphims (SNPs) genotypic profiling of Malay patients with and without Helicobacter pylori infection in Kelantan, 2011) and one SNP from GWAS study. In addition, the analysis also reveals that both Royal Kelantan Malay genomes shared 3 SNP markers; HBG1 (rs1061234), HBB (rs1609812) and BCL11A (rs766432) where all three markers were associated with beta-thalassemia.

conclusionsOur findings suggest that the Royal Kelantan Malays carry the SNPs which are associated with protection to Helicobacter pylori infection. In addition they also carry SNPs which are associated with beta-thalassemia. These findings are in line with the findings by other researchers who conducted studies on thalassemia and Helicobacter pylori infection in the non-royal Malay population.

Indexed as

Beta-thalassemiaHelicobacter pyloriMalaysSingle nucleotide polymorphismsWhole genome analysis

Identifiers

PMID27090252
PMCPMC4685156
OpenAlexW2143349097

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Registered trials

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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.