Uncovering Disease-Related Polymorphisms through Correlations between SNP Frequencies, Population and Epidemiological Data
Background: According to GWAS, which analyzes large amounts of DNA variants in case-control strategies, the genetic differences between two human individuals do not exceed 0.5%. As a consequence, finding biological significance in GWAS results is a challenging task. We propose an alternative method...
Main Authors: | Samara Marques Dos Reis, Cristhian Augusto Bugs, José Artur Bogo Chies, Andrés Delgado Cañedo |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-06-01
|
Series: | BioMedInformatics |
Subjects: | |
Online Access: | https://www.mdpi.com/2673-7426/3/2/32 |
Similar Items
-
SNPMap—An integrated visual SNP interpretation tool
by: Miaosen Liu, et al.
Published: (2022-08-01) -
Human Genetic Bi-allelic Sequences, HGBASE, a Database of Intra-genic Polymorphisms
by: Sarkar Chandra, et al.
Published: (1998-01-01) -
Pathogenic Single Nucleotide Polymorphisms on Autophagy-Related Genes
by: Isaac Tamargo-Gómez, et al.
Published: (2020-11-01) -
Genetic Polymorphisms Associated with Valproic Acid Therapy: Review article
by: Reham A.M. Ellisy*, et al.
Published: (2022-07-01) -
Association of Metabolic Syndrome with Aerobic Exercise and LPL rs3779788 Polymorphism in Taiwan Biobank Individuals
by: Hsu CS, et al.
Published: (2021-09-01)