Javascript must be enabled to continue!
JLOH: Inferring Loss of Heterozygosity Blocks from Sequencing Data
View through CrossRef
AbstractHeterozygosity is a genetic condition in which two or more alleles are found at a genomic locus. Among the organisms that are more prone to heterozygosity are hybrids, i.e. organisms that are the offspring of genetically divergent yet still interfertile individuals. One of the most studied aspects is the loss of heterozygosity (LOH) within genomes, where multi-allelic sites lose one of their two alleles by converting it to the other, or by remaining hemizygous at that site. LOH is deeply interconnected with adaptation, especially in hybrids, but thein silicotechniques to infer LOH blocks are hardly standardized, and a general tool to infer and analyse them in most genomic contexts and species is missing. Here, we present JLOH, a computational toolkit for the inference and exploration of LOH blocks which only requires commonly available genomic data as input. Starting from mapped reads, called variants and a reference genome sequence, JLOH infers candidate LOH blocks based on single-nucleotide polymorphism density (SNPs/kbp) and read coverage per position. If working with a hybrid organism of known parentals, JLOH is also able to assign each LOH block to its subgenome of origin.
Cold Spring Harbor Laboratory
Title: JLOH: Inferring Loss of Heterozygosity Blocks from Sequencing Data
Description:
AbstractHeterozygosity is a genetic condition in which two or more alleles are found at a genomic locus.
Among the organisms that are more prone to heterozygosity are hybrids, i.
e.
organisms that are the offspring of genetically divergent yet still interfertile individuals.
One of the most studied aspects is the loss of heterozygosity (LOH) within genomes, where multi-allelic sites lose one of their two alleles by converting it to the other, or by remaining hemizygous at that site.
LOH is deeply interconnected with adaptation, especially in hybrids, but thein silicotechniques to infer LOH blocks are hardly standardized, and a general tool to infer and analyse them in most genomic contexts and species is missing.
Here, we present JLOH, a computational toolkit for the inference and exploration of LOH blocks which only requires commonly available genomic data as input.
Starting from mapped reads, called variants and a reference genome sequence, JLOH infers candidate LOH blocks based on single-nucleotide polymorphism density (SNPs/kbp) and read coverage per position.
If working with a hybrid organism of known parentals, JLOH is also able to assign each LOH block to its subgenome of origin.
Related Results
Diagnostic blocks for chronic pain
Diagnostic blocks for chronic pain
Abstract
Many conditions associated with chronic pain have no detectable morphological correlate. Consequently, the source of pain cannot be established by clinical ...
Development of lightweight building blocks using expanded polystyrene
Development of lightweight building blocks using expanded polystyrene
This study aimed to develop lightweight building blocks using Expanded Polystyrene (EPS) with varying percentages, assess their properties, including density, water absorption, por...
Blocks Size Frequency Distribution in the Tiger Stripes area (Enceladus)
Blocks Size Frequency Distribution in the Tiger Stripes area (Enceladus)
IntroductionEnceladus is a heavily cratered, ~500 km-size icy moon of Saturn [1], orbiting at ~4 Saturn radii from the planet. In 2005, the Cassini ISS-NAC camera [2] took high-res...
Lithic Inclusions in the Taupo Pumice Formation
Lithic Inclusions in the Taupo Pumice Formation
<p>The Taupo Pumice Formation is a product of the Taupo eruption of about 1800a, and consists of three phreatomagmatic ash deposits, two plinian pumice deposits and a major l...
MARS-seq2.0: an experimental and analytical pipeline for indexed sorting combined with single-cell RNA sequencing v1
MARS-seq2.0: an experimental and analytical pipeline for indexed sorting combined with single-cell RNA sequencing v1
Human tissues comprise trillions of cells that populate a complex space of molecular phenotypes and functions and that vary in abundance by 4–9 orders of magnitude. Relying solely ...
HLA Genetic Diversity and Chronic Hepatitis B Virus Infection: Effect of Heterozygosity Advantage
HLA Genetic Diversity and Chronic Hepatitis B Virus Infection: Effect of Heterozygosity Advantage
This research aims to determine whether HLA heterozygosity confers a protective effect against hepatitis B virus infection by analyzing the relationship between HLA diversity and t...
Accurately estimating the homologous recombination deficiency based on low-pass whole-genome sequencing and target sequencing.
Accurately estimating the homologous recombination deficiency based on low-pass whole-genome sequencing and target sequencing.
e15077 Background: Homologous recombination deficiency (HRD) is a promising biomarker for poly ADP-ribose polymerase (PARP) inhibitors. In the past, the HRD status was mainly esti...
Effects of Waterlogging on Soybean Rhizosphere Microbial Community Profiled Using Illumina MiSeq, LoopSeq, and PacBio 16S rRNA Genes Sequences
Effects of Waterlogging on Soybean Rhizosphere Microbial Community Profiled Using Illumina MiSeq, LoopSeq, and PacBio 16S rRNA Genes Sequences
Abstract
Background: Waterlogging on the global environment has led to a significant decline in crop yields. However, the response of plant-associated microbes to waterlogg...

