Add to ORKGWhole genome duplications followed by differentiation of many gene duplicates in the ancestors of rainbow quantitative genetics fundamentally rely on the accurate identification of the alleles of a gene or locus [13]. Christensen et al. BMC Bioinformatics 2013, 14:32
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Large scale gene duplication is a major force driving the evolution of genetic functional innovation...
Sequencing family DNA samples provides an attractive alternative to population based de-signs to ide...
Full list of author information is available at the end of the articleBackground Gene duplications h...
Identification of human haploinsufficient genes and their genomic proximity to segmental duplication
Gene duplication has had a significant impact on all genomes and the human genome is no exception, a...
Background: Variations in DNA copy number carry information on the modalities of genome evolution an...
Genotype imputation is a key step in the analysis of genome-wide association studies (GWAS) and geno...
Background: Multi-allelic copy number variants include examples of extensive variation between indiv...
Background: Almost all genome sequencing projects neglect the fact that diploid organisms contain tw...
Genetics research has increased rapidly with availability of high throughput molecular biology tools...
Ancestral allele information is useful for genetics studies. Previously, the identification of an-ce...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
Abstract: Meiosis and recombination are the two opposite aspects that coexist in a DNA system. As a ...
Full list of author information is available at the end of the articleIntroduction Single Nucleotide...
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Large scale gene duplication is a major force driving the evolution of genetic functional innovation...
Sequencing family DNA samples provides an attractive alternative to population based de-signs to ide...
Full list of author information is available at the end of the articleBackground Gene duplications h...
Identification of human haploinsufficient genes and their genomic proximity to segmental duplication
Gene duplication has had a significant impact on all genomes and the human genome is no exception, a...
Background: Variations in DNA copy number carry information on the modalities of genome evolution an...
Genotype imputation is a key step in the analysis of genome-wide association studies (GWAS) and geno...
Background: Multi-allelic copy number variants include examples of extensive variation between indiv...
Background: Almost all genome sequencing projects neglect the fact that diploid organisms contain tw...
Genetics research has increased rapidly with availability of high throughput molecular biology tools...
Ancestral allele information is useful for genetics studies. Previously, the identification of an-ce...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
Abstract: Meiosis and recombination are the two opposite aspects that coexist in a DNA system. As a ...
Full list of author information is available at the end of the articleIntroduction Single Nucleotide...
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Large scale gene duplication is a major force driving the evolution of genetic functional innovation...
Sequencing family DNA samples provides an attractive alternative to population based de-signs to ide...