a<p>Number of reads used for assemblage. <sup>b</sup>Number of reads assembled into contigs. <sup>c</sup>Number of contigs longer than 1000 bp. <sup>d</sup>Length of the longest contig.</p
<p>The terms ‘no break’ and ‘break 500’ refer to whether or not contigs were broken up by deleting r...
The Department of Energy Joint Genome Institute (www.jgi.doe.gov) in Walnut Creek, CA is a high thro...
<p>The x-axis indicates sequence sizes from 200 bp to ≥ 5000 bp with a bin size of 100; the y-axis i...
<p>Number of reads per sample represents only those from which the indicator MID sequence was recove...
<p>Summary of assembly, BLAST and annotation of sequences resulting from 454 sequencing.</p
<p>Reads of cDNA sequencing by 454-GS-FLX Titanium technology were assembled by MIRA assembly progra...
<p>All Illumina reads of non-challenged (NC), challenged-mild pathology (MD) and challenged-severe p...
<p>Description of different properties of sequenced transcripts, assembly and annotation.</p
1<p>- for Sanger reads there were no contigs assembled from combining more than one read, therefore ...
<p>A) number of sequences successfully barcoded for each of the eight ascertainment individuals; and...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
<p>Length distribution (bp) of the 38,297 contigs of the global 454 assembly.</p
<p>Length distribution of <i>de </i><i>novo</i> assemblies of isotigs (x-axis indicates the sequence...
<p>Mean length: Mean length of the assembled sequences. N50: The length of the contig or unigene cor...
1<p>Characteristics of sequence data used in the assembly.</p>2<p>Results of the original assembly b...
<p>The terms ‘no break’ and ‘break 500’ refer to whether or not contigs were broken up by deleting r...
The Department of Energy Joint Genome Institute (www.jgi.doe.gov) in Walnut Creek, CA is a high thro...
<p>The x-axis indicates sequence sizes from 200 bp to ≥ 5000 bp with a bin size of 100; the y-axis i...
<p>Number of reads per sample represents only those from which the indicator MID sequence was recove...
<p>Summary of assembly, BLAST and annotation of sequences resulting from 454 sequencing.</p
<p>Reads of cDNA sequencing by 454-GS-FLX Titanium technology were assembled by MIRA assembly progra...
<p>All Illumina reads of non-challenged (NC), challenged-mild pathology (MD) and challenged-severe p...
<p>Description of different properties of sequenced transcripts, assembly and annotation.</p
1<p>- for Sanger reads there were no contigs assembled from combining more than one read, therefore ...
<p>A) number of sequences successfully barcoded for each of the eight ascertainment individuals; and...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
<p>Length distribution (bp) of the 38,297 contigs of the global 454 assembly.</p
<p>Length distribution of <i>de </i><i>novo</i> assemblies of isotigs (x-axis indicates the sequence...
<p>Mean length: Mean length of the assembled sequences. N50: The length of the contig or unigene cor...
1<p>Characteristics of sequence data used in the assembly.</p>2<p>Results of the original assembly b...
<p>The terms ‘no break’ and ‘break 500’ refer to whether or not contigs were broken up by deleting r...
The Department of Energy Joint Genome Institute (www.jgi.doe.gov) in Walnut Creek, CA is a high thro...
<p>The x-axis indicates sequence sizes from 200 bp to ≥ 5000 bp with a bin size of 100; the y-axis i...
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