<p>The sequence assembly is shown with dark grey boxes representing sequence contigs. Contigs were bridged by paired-end sequence reads. The genome map is represented by light grey boxes. Shaded boxes around regions of both maps denote regions where the sequence assembly matches the genome map well. Regions where there are significant discrepancies are numbered and discussed in the results section. The two gaps in the genome map are denoted with asterisks.</p
<p>a) <b>Contig Length Distribution.</b> Histograms of the contig lengths illustrate the number of c...
De novo genome assembly is always fragmented. Assembly fragmentation is more serious using the popul...
The development of “next-generation” high-throughput sequencing technologies has made it possible fo...
<p>The final sequence assembly almost completely spans the genome map. Gaps in the genome map are de...
<p>The target genome is shown in the center, aligned to two related genomes, A and B. The DNA sequen...
<p>Comparison of genome assembly results derived from different sequencing technologies and assembly...
<p>The original assembly contained two Nt.BspQI sites and ∼8 kb of sequence that were absent from th...
<p>The top line represents the <i>in silico</i> map for the original sequence assembly, the majority...
<p>Assembly quality is assessed by (a) the number of gaps in the draft assemblies, and (b) gap size ...
<p>The terms ‘no break’ and ‘break 500’ refer to whether or not contigs were broken up by deleting r...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
<p>Panel A shows the strip diagram for one of the clones that covers the high density region, each l...
Abstract Background Reference genome assemblies are valuable, as they provide insights into gene con...
<p><b>Copyright information:</b></p><p>Taken from "Optical mapping as a routine tool for bacterial g...
The gene order of the chloroplast genome of Podocarpus macrophylla has been determined twice -- once...
<p>a) <b>Contig Length Distribution.</b> Histograms of the contig lengths illustrate the number of c...
De novo genome assembly is always fragmented. Assembly fragmentation is more serious using the popul...
The development of “next-generation” high-throughput sequencing technologies has made it possible fo...
<p>The final sequence assembly almost completely spans the genome map. Gaps in the genome map are de...
<p>The target genome is shown in the center, aligned to two related genomes, A and B. The DNA sequen...
<p>Comparison of genome assembly results derived from different sequencing technologies and assembly...
<p>The original assembly contained two Nt.BspQI sites and ∼8 kb of sequence that were absent from th...
<p>The top line represents the <i>in silico</i> map for the original sequence assembly, the majority...
<p>Assembly quality is assessed by (a) the number of gaps in the draft assemblies, and (b) gap size ...
<p>The terms ‘no break’ and ‘break 500’ refer to whether or not contigs were broken up by deleting r...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
<p>Panel A shows the strip diagram for one of the clones that covers the high density region, each l...
Abstract Background Reference genome assemblies are valuable, as they provide insights into gene con...
<p><b>Copyright information:</b></p><p>Taken from "Optical mapping as a routine tool for bacterial g...
The gene order of the chloroplast genome of Podocarpus macrophylla has been determined twice -- once...
<p>a) <b>Contig Length Distribution.</b> Histograms of the contig lengths illustrate the number of c...
De novo genome assembly is always fragmented. Assembly fragmentation is more serious using the popul...
The development of “next-generation” high-throughput sequencing technologies has made it possible fo...