<p>The BWA tools mapped original 100 bp reads to the scaffold of all ABySS_55 sequences with criteria that the matches had > = 95% length and > = 90% identity. In this Figure, the top panel shows reference transcripts. The bottom panel shows coverage as the number of reads per nucleotide position in the reference genes. As shown in this example, many parts of the assembled sequences had coverage higher than 200.</p
Percentage of genome covered by contigs assembled by different assembly strategies. Covered genome f...
<p><i>Sample collection</i>. A biological sample (e.g., blood) is collected. <i>Culture</i>. Bacteri...
<p>The coverage within contigs is calculated by dividing the total number of base pairs contained in...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
The reference sequences play an essential role in genome assembly, like type specimens in taxonomy. ...
The mapping statistics are displayed herein including the number of clean reads mapped to the refere...
<p>The figure shows the average sequence coverage (y-axis, in read per base) of each <i>de novo</i> ...
<p>1 The number of uniquely mapped reads after filtering for PCR duplicates.</p><p>2 Reference seque...
Illumina sequencing has revolutionized yeast genomics, with prices for commercial draft genome seque...
<p><b>Library</b>: id of library. <b>Length (nt)</b>: Length of scaffold in nucleotides. <b>Average ...
<p>(a) Dot-plot alignments of assembled scaffolds vs the reference genome sequence of <i>Aspergillus...
Genomic research relies on computers to process large amounts of genomic data. In order to digitize ...
<p>“Total Reads” indicates the number of 36-nt reads generated for each strain by Illumina GAII sequ...
<p>The sequence assembly is shown with dark grey boxes representing sequence contigs. Contigs were b...
Percentage of genome covered by contigs assembled by different assembly strategies. Covered genome f...
<p><i>Sample collection</i>. A biological sample (e.g., blood) is collected. <i>Culture</i>. Bacteri...
<p>The coverage within contigs is calculated by dividing the total number of base pairs contained in...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
The reference sequences play an essential role in genome assembly, like type specimens in taxonomy. ...
The mapping statistics are displayed herein including the number of clean reads mapped to the refere...
<p>The figure shows the average sequence coverage (y-axis, in read per base) of each <i>de novo</i> ...
<p>1 The number of uniquely mapped reads after filtering for PCR duplicates.</p><p>2 Reference seque...
Illumina sequencing has revolutionized yeast genomics, with prices for commercial draft genome seque...
<p><b>Library</b>: id of library. <b>Length (nt)</b>: Length of scaffold in nucleotides. <b>Average ...
<p>(a) Dot-plot alignments of assembled scaffolds vs the reference genome sequence of <i>Aspergillus...
Genomic research relies on computers to process large amounts of genomic data. In order to digitize ...
<p>“Total Reads” indicates the number of 36-nt reads generated for each strain by Illumina GAII sequ...
<p>The sequence assembly is shown with dark grey boxes representing sequence contigs. Contigs were b...
Percentage of genome covered by contigs assembled by different assembly strategies. Covered genome f...
<p><i>Sample collection</i>. A biological sample (e.g., blood) is collected. <i>Culture</i>. Bacteri...
<p>The coverage within contigs is calculated by dividing the total number of base pairs contained in...