<p>UTR = untranslated region, SNV = single nucleotide variation, DIV = deletion/insertion variation, chr = chromosome, array = capture array, spl site = splice site, prom = promoter.</p
<p>Chr: chromosome; Ref: reference base; Obs: observed base; NCBI RS: NCBI Reference Sequence; Varia...
Abstract Background The fidelity of DNA replication serves as the nidus for both genetic evolution a...
<p>Nucleotide variants called in sample 178-3 relative to ancestral 178-2 genome 97 d post-sampling—...
<p>Selected single nucleotide variants of the candidate genes, their allele frequencies and Hardy–We...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
<p>Detailed procedure was described in <i>Materials and Methods</i>. The URLs for the locus-specific...
Systematic filtering of single nucleotide variants called from CLC workbench with number of variants...
In this study, we analyze the Genetic Analysis Workshop 17 data to identify regions of single-nucleo...
<p>Gene-based association results for rare variant analyses in the chr 7p region, for genes with p<0...
<p>List of final candidate variants passing all filters.</p>a<p>Chromosome in which the variant was ...
HumanHap550 Genotyping BeadChip provides a platform allowing for genotyping of single nucleotide pol...
Filtered SNPs that have undergone VariantFiltration and also selection for presence in 75% of indivi...
Background: Single nucleotide polymorphisms (SNPs) are DNA sequence variations, occ...
<p>h haplotypes</p><p>Hd haplotype diversity</p><p>k average number of nucleotide differences</p><p>...
<p>Chr: chromosome; Ref: reference base; Obs: observed base; NCBI RS: NCBI Reference Sequence; Varia...
Abstract Background The fidelity of DNA replication serves as the nidus for both genetic evolution a...
<p>Nucleotide variants called in sample 178-3 relative to ancestral 178-2 genome 97 d post-sampling—...
<p>Selected single nucleotide variants of the candidate genes, their allele frequencies and Hardy–We...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
<p>Detailed procedure was described in <i>Materials and Methods</i>. The URLs for the locus-specific...
Systematic filtering of single nucleotide variants called from CLC workbench with number of variants...
In this study, we analyze the Genetic Analysis Workshop 17 data to identify regions of single-nucleo...
<p>Gene-based association results for rare variant analyses in the chr 7p region, for genes with p<0...
<p>List of final candidate variants passing all filters.</p>a<p>Chromosome in which the variant was ...
HumanHap550 Genotyping BeadChip provides a platform allowing for genotyping of single nucleotide pol...
Filtered SNPs that have undergone VariantFiltration and also selection for presence in 75% of indivi...
Background: Single nucleotide polymorphisms (SNPs) are DNA sequence variations, occ...
<p>h haplotypes</p><p>Hd haplotype diversity</p><p>k average number of nucleotide differences</p><p>...
<p>Chr: chromosome; Ref: reference base; Obs: observed base; NCBI RS: NCBI Reference Sequence; Varia...
Abstract Background The fidelity of DNA replication serves as the nidus for both genetic evolution a...
<p>Nucleotide variants called in sample 178-3 relative to ancestral 178-2 genome 97 d post-sampling—...