2015
DOI: 10.4172/2161-1041.1000142
|View full text |Cite
|
Sign up to set email alerts
|

Population Genetics for Autosomal STR Loci in Sikh Population of Central India

Abstract: This study is an attempt to generate genetic database for three endogamous populations of Sikh population (Arora, Jat and Ramgariha) of Central India. The analysis of eight autosomal STR loci (D16S539, D7S820, D13S317, FGA, CSF1PO, D21S11, D18S51, and D2S1338) was done in 140 unrelated Sikh individuals. In all the three studied populations, all loci were in Hardy -Weinberg equilibrium except at locus FGA in Ramgariha Sikh and locus D16S539 in Arora Sikh. An analysis of molecular variance (AMOVA) showed 1% vari… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2015
2015
2020
2020

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 28 publications
0
1
0
Order By: Relevance
“…A population analysis can be performed using the model based STRUCTURE program using available genomic data. The program can infer the genetic structure in haploid, diploid and polyploid species as per requirement [44,45]. Simulation studies in population genetics play an important role in helping to better understand the impact of various evolutionary and demographic scenarios on sequence variation and sequence patterns, and they also permit investigators to better assess and design analytical methods in the study of disease-associated genetic factors.…”
Section: Bioinformatics Methods For Viral Genomicsmentioning
confidence: 99%
“…A population analysis can be performed using the model based STRUCTURE program using available genomic data. The program can infer the genetic structure in haploid, diploid and polyploid species as per requirement [44,45]. Simulation studies in population genetics play an important role in helping to better understand the impact of various evolutionary and demographic scenarios on sequence variation and sequence patterns, and they also permit investigators to better assess and design analytical methods in the study of disease-associated genetic factors.…”
Section: Bioinformatics Methods For Viral Genomicsmentioning
confidence: 99%