<p>For each segment, the total number of DNA mismatches between individuals within a household (H) and sequences obtained from the same individual on separate days (I) is indicated (cf <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0043742#pone-0043742-t001" target="_blank">Table 1</a>). “–” indicates where data was unavailable.</p
Summary: A general algorithm is described for haplotype analysis of unrelated individuals with missi...
Background: A feature common to all DNA sequencing technologies is the presence of base-call errors ...
<p>Frequency of genotypes with missing data (left), and frequency of DArTseq SNPs (loci) with missin...
<p>Mismatch distributions of cpDNA haplotypes based on pairwise sequence difference plotted against ...
a<p>Sites could not be analyzed due to missing sequence data.</p>b<p>Partial sequence of this region...
<p>Genotype missing rates and numbers of pairs of related samples reported in submitted pedigree fil...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
<p>Comparisons were made for each phylum. One and two or more mismatches were estimated independentl...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
<p>Comparisons were made for each phylum. One and two or more mismatches were estimated independentl...
The most prevalent mechanisms leading to mutations in DNA are direct mis-incorporation of bases duri...
<p>(<b>a</b>) We identified a novel error mode based on visual examination of disputed SNPs. As show...
The most prevalent mechanisms leading to mutations in DNA are direct mis-incorporation of bases duri...
Summary: A general algorithm is described for haplotype analysis of unrelated individuals with missi...
Background: A feature common to all DNA sequencing technologies is the presence of base-call errors ...
<p>Frequency of genotypes with missing data (left), and frequency of DArTseq SNPs (loci) with missin...
<p>Mismatch distributions of cpDNA haplotypes based on pairwise sequence difference plotted against ...
a<p>Sites could not be analyzed due to missing sequence data.</p>b<p>Partial sequence of this region...
<p>Genotype missing rates and numbers of pairs of related samples reported in submitted pedigree fil...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
<p>Comparisons were made for each phylum. One and two or more mismatches were estimated independentl...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
The high throughput of data arising from the complete sequence of the human genome has left statisti...
<p>Comparisons were made for each phylum. One and two or more mismatches were estimated independentl...
The most prevalent mechanisms leading to mutations in DNA are direct mis-incorporation of bases duri...
<p>(<b>a</b>) We identified a novel error mode based on visual examination of disputed SNPs. As show...
The most prevalent mechanisms leading to mutations in DNA are direct mis-incorporation of bases duri...
Summary: A general algorithm is described for haplotype analysis of unrelated individuals with missi...
Background: A feature common to all DNA sequencing technologies is the presence of base-call errors ...
<p>Frequency of genotypes with missing data (left), and frequency of DArTseq SNPs (loci) with missin...