Systematic filtering of single nucleotide variants called from CLC workbench with number of variants remaining after each step and criteria for retaining variant as indicated.</p
<p>Mean number of variants remaining at each stage of post-sequencing filtering.</p
Preliminary candidate variants genotyping and distribution through the members of the reported famil...
<p>Exon constitutes coding variants only. Splice junction constitutes +/−5 bp around an exon. A full...
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
A critical step in detecting variants from next-generation sequencing data is post hoc filtering of ...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
<div><p>A critical step in detecting variants from next-generation sequencing data is <em>post hoc</...
The scheme outlines a typical candidate disease variant filtering strategy whereby successive filter...
<p>Nucleotide variant information for re-sequencing projects conducted in current study.</p
<p>Number of variants and genes present after initial filtering and biological filtering.</p
<p>Each step of the filtering process and the number of SNPs remaining are shown in sequence. Putati...
<p>UTR = untranslated region, SNV = single nucleotide variation, DIV = deletion/insertion variati...
<p>Overview of variant filtering to identify gCJD-related genes and gene variants. Each stage was pr...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
<p>Mean number of variants remaining at each stage of post-sequencing filtering.</p
Preliminary candidate variants genotyping and distribution through the members of the reported famil...
<p>Exon constitutes coding variants only. Splice junction constitutes +/−5 bp around an exon. A full...
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
A critical step in detecting variants from next-generation sequencing data is post hoc filtering of ...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
<div><p>A critical step in detecting variants from next-generation sequencing data is <em>post hoc</...
The scheme outlines a typical candidate disease variant filtering strategy whereby successive filter...
<p>Nucleotide variant information for re-sequencing projects conducted in current study.</p
<p>Number of variants and genes present after initial filtering and biological filtering.</p
<p>Each step of the filtering process and the number of SNPs remaining are shown in sequence. Putati...
<p>UTR = untranslated region, SNV = single nucleotide variation, DIV = deletion/insertion variati...
<p>Overview of variant filtering to identify gCJD-related genes and gene variants. Each stage was pr...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
Title Filtering of coding and non-coding genetic variants Description Filter genetic variants using ...
<p>Mean number of variants remaining at each stage of post-sequencing filtering.</p
Preliminary candidate variants genotyping and distribution through the members of the reported famil...
<p>Exon constitutes coding variants only. Splice junction constitutes +/−5 bp around an exon. A full...
DOI
Add to ORKG