<p>Variant filtering representation through the number of SNPs remaining after the various filtering steps.</p><p>The Average and Percentage remaining rows represent the average number of variants and percentage of variants remaining per family.</p>a<p>Intronic, intergenic and synonymous variants were discarded. See methods.</p>b<p>Detailed criteria for these filters is reported on the methods section.</p>c<p>Number of variants shared between the two individuals in the family.</p>d<p>Total number of final variants for all the individuals in this study.</p
These SNPs were called from 109 Metchnikowia sp whole genomes mapped to MR_a10 reference genome usin...
Genome-wide association studies have successfully identified associations between common diseases an...
<p>Subpanels (A) and (B) contain contour plots showing the proportion of heritability explained () b...
<p>Variant filtering representation through the number of INDELs remaining after the various filteri...
Plot over number of shared candidate disease-causing variants when successively adding up to 11 affe...
<p>These graphs compare the number of variants per person at different stages of the literature scre...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>Average number of variants remaining per sample after sequential or aggregate filtering steps.</p...
<p>The Combined Filter sequentially applies all the filters described in this study. Vertical colore...
The scheme outlines a typical candidate disease variant filtering strategy whereby successive filter...
Genome-wide association studies have successfully identified associations between common diseases an...
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>Total SNP counts were classified by genomic location (Intergenic vs. Genic) and further separated...
Abstract In studies of families with rare disease, it is common to screen for de novo mutations, as ...
These SNPs were called from 109 Metchnikowia sp whole genomes mapped to MR_a10 reference genome usin...
Genome-wide association studies have successfully identified associations between common diseases an...
<p>Subpanels (A) and (B) contain contour plots showing the proportion of heritability explained () b...
<p>Variant filtering representation through the number of INDELs remaining after the various filteri...
Plot over number of shared candidate disease-causing variants when successively adding up to 11 affe...
<p>These graphs compare the number of variants per person at different stages of the literature scre...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>Average number of variants remaining per sample after sequential or aggregate filtering steps.</p...
<p>The Combined Filter sequentially applies all the filters described in this study. Vertical colore...
The scheme outlines a typical candidate disease variant filtering strategy whereby successive filter...
Genome-wide association studies have successfully identified associations between common diseases an...
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>Total SNP counts were classified by genomic location (Intergenic vs. Genic) and further separated...
Abstract In studies of families with rare disease, it is common to screen for de novo mutations, as ...
These SNPs were called from 109 Metchnikowia sp whole genomes mapped to MR_a10 reference genome usin...
Genome-wide association studies have successfully identified associations between common diseases an...
<p>Subpanels (A) and (B) contain contour plots showing the proportion of heritability explained () b...