<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding of contigs using 38×2 bp mate-pair reads (insert size 4–6 kb). Three random subsets of reads were analyzed for each coverage level except the highest, which used all of the reads.</p
a<p>Number of reads used for assemblage. <sup>b</sup>Number of reads assembled into contigs. <sup>c<...
<p>All Illumina reads of non-challenged (NC), challenged-mild pathology (MD) and challenged-severe p...
a<p>Values after r-sampling; estimated based on the genome size of RIB40 (37 Mb).</p>b<p>Estimated f...
1<p>- for Sanger reads there were no contigs assembled from combining more than one read, therefore ...
<p>The figure shows the average sequence coverage (y-axis, in read per base) of each <i>de novo</i> ...
<p>The length distributions of <i>de novo</i> assemblies of contigs, scaffolds and unigenes are show...
<p>Number of reads per sample represents only those from which the indicator MID sequence was recove...
<p>The length distribution of the assembled sequences are showed in <a href="http://www.plosone.org/...
<p>a) <b>Contig Length Distribution.</b> Histograms of the contig lengths illustrate the number of c...
<p>1 The number of uniquely mapped reads after filtering for PCR duplicates.</p><p>2 Reference seque...
<p>Length distribution of <i>de </i><i>novo</i> assemblies of isotigs (x-axis indicates the sequence...
<p>The BWA tools mapped original 100 bp reads to the scaffold of all ABySS_55 sequences with criteri...
<p>Data is shown for the six sequencing methods with more than 5 projects. Indicated are the range f...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
<p>Human chr21 (34.2 Mb), Total error rate = 1.0%</p><p>We varied the average read length from 100 t...
a<p>Number of reads used for assemblage. <sup>b</sup>Number of reads assembled into contigs. <sup>c<...
<p>All Illumina reads of non-challenged (NC), challenged-mild pathology (MD) and challenged-severe p...
a<p>Values after r-sampling; estimated based on the genome size of RIB40 (37 Mb).</p>b<p>Estimated f...
1<p>- for Sanger reads there were no contigs assembled from combining more than one read, therefore ...
<p>The figure shows the average sequence coverage (y-axis, in read per base) of each <i>de novo</i> ...
<p>The length distributions of <i>de novo</i> assemblies of contigs, scaffolds and unigenes are show...
<p>Number of reads per sample represents only those from which the indicator MID sequence was recove...
<p>The length distribution of the assembled sequences are showed in <a href="http://www.plosone.org/...
<p>a) <b>Contig Length Distribution.</b> Histograms of the contig lengths illustrate the number of c...
<p>1 The number of uniquely mapped reads after filtering for PCR duplicates.</p><p>2 Reference seque...
<p>Length distribution of <i>de </i><i>novo</i> assemblies of isotigs (x-axis indicates the sequence...
<p>The BWA tools mapped original 100 bp reads to the scaffold of all ABySS_55 sequences with criteri...
<p>Data is shown for the six sequencing methods with more than 5 projects. Indicated are the range f...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
<p>Human chr21 (34.2 Mb), Total error rate = 1.0%</p><p>We varied the average read length from 100 t...
a<p>Number of reads used for assemblage. <sup>b</sup>Number of reads assembled into contigs. <sup>c<...
<p>All Illumina reads of non-challenged (NC), challenged-mild pathology (MD) and challenged-severe p...
a<p>Values after r-sampling; estimated based on the genome size of RIB40 (37 Mb).</p>b<p>Estimated f...