Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Loter: A software package to infer local ancestry for a wide range of species

View through CrossRef
Abstract Admixture between populations provides opportunity to study biological adaptation and phenotypic variation. Admixture studies rely on local ancestry inference for admixed individuals, which consists of computing at each locus the number of copies that originate from ancestral source populations. Existing software packages for local ancestry inference are tuned to provide accurate results on human data and recent admixture events. Here, we introduce Loter, an open-source software package that does not require any biological parameter besides haplotype data in order to make local ancestry inference available for a wide range of species. Using simulations, we compare the performance of Loter to HAPMIX, LAMP-LD, and RFMix. HAPMIX is the only software severely impacted by imperfect haplotype reconstruction. Loter is the less impacted software by increasing admixture time when considering simulated and admixed human genotypes. For simulations of admixed Populus genotypes, Loter and LAMP-LD are robust to increasing admixture times by contrast to RFMix. When comparing length of reconstructed and true ancestry tracts, Loter and LAMP-LD provide results whose accuracy is again more robust than RFMix to increasing admixture times. We apply Loter to individuals resulting from admixture between Populus trichocarpa and Populus balsamifera and lengths of ancestry tracts indicate that admixture took place around 100 generations ago. We expect that providing a rapid and parameter-free software for local ancestry inference will make more accessible genomic studies about admixture processes.
Title: Loter: A software package to infer local ancestry for a wide range of species
Description:
Abstract Admixture between populations provides opportunity to study biological adaptation and phenotypic variation.
Admixture studies rely on local ancestry inference for admixed individuals, which consists of computing at each locus the number of copies that originate from ancestral source populations.
Existing software packages for local ancestry inference are tuned to provide accurate results on human data and recent admixture events.
Here, we introduce Loter, an open-source software package that does not require any biological parameter besides haplotype data in order to make local ancestry inference available for a wide range of species.
Using simulations, we compare the performance of Loter to HAPMIX, LAMP-LD, and RFMix.
HAPMIX is the only software severely impacted by imperfect haplotype reconstruction.
Loter is the less impacted software by increasing admixture time when considering simulated and admixed human genotypes.
For simulations of admixed Populus genotypes, Loter and LAMP-LD are robust to increasing admixture times by contrast to RFMix.
When comparing length of reconstructed and true ancestry tracts, Loter and LAMP-LD provide results whose accuracy is again more robust than RFMix to increasing admixture times.
We apply Loter to individuals resulting from admixture between Populus trichocarpa and Populus balsamifera and lengths of ancestry tracts indicate that admixture took place around 100 generations ago.
We expect that providing a rapid and parameter-free software for local ancestry inference will make more accessible genomic studies about admixture processes.

Related Results

Abstract 1166: Leveraging existing data to identify ancestry-associated features across multiple cancer types
Abstract 1166: Leveraging existing data to identify ancestry-associated features across multiple cancer types
Abstract People with different ancestries inherit different risks and encounter different environmental exposures resulting in different somatic profiles. A lack of ...
Abstract 1599: Determining patient ancestry based on targeted tumor comprehensive genomic profiling
Abstract 1599: Determining patient ancestry based on targeted tumor comprehensive genomic profiling
Abstract Background. Cancer gene mutations exhibit mutation patterns of prevalence that vary across different ancestry groups. For example, EGFR variants are more fr...
Data from Blood Vitamin D Levels in Relation to Genetic Estimation of African Ancestry
Data from Blood Vitamin D Levels in Relation to Genetic Estimation of African Ancestry
<div>Abstract<p><b>Background:</b> African-Americans generally have lower circulating levels of 25 hydroxyvitamin D [25(OH)D] than Whites, attributed to ski...
Data from Blood Vitamin D Levels in Relation to Genetic Estimation of African Ancestry
Data from Blood Vitamin D Levels in Relation to Genetic Estimation of African Ancestry
<div>Abstract<p><b>Background:</b> African-Americans generally have lower circulating levels of 25 hydroxyvitamin D [25(OH)D] than Whites, attributed to ski...
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Impacts of man-made structures on marine biodiversity and species status - native & non-native species
Impacts of man-made structures on marine biodiversity and species status - native & non-native species
<p>Coastal environments are exposed to anthropogenic activities such as frequent marine traffic and restructuring, i.e., addition, removal or replacing with man-made structur...
Arthritis and Rheumatism
Arthritis and Rheumatism
OBJECTIVE: To determine whether genetic substructure in European-derived populations is associated with specific manifestations of systemic lupus erythematosus (SLE), including muc...

Back to Top