<p>This figure reports F1 measure varying sequencing error from 0% to 6% for 250 thousands of 75 bp reads mapped against the build 37.3 of the human genome.</p
The x-axis shows the base position within a sequencing read, and the y-axis shows the average error ...
<p>(A) Percentage of small RNA reads from each genotype by size. (B) Percentages of small RNA reads ...
<p>The paternal and maternal genomes differes in 1% SNPs. The mean insert size is 250bp with 25bp st...
<p>This figure reports F1 measure varying sequencing error from 0% to 6% for 250 thousands of 120 bp...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 75 bp rea...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 120 bp re...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 75 bp rea...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
<p>(A) shows the sequencing errors occur randomly across one read and B) shows the error rate is alm...
<p>(A), 2- to 35-kb libraries; (B), 10 kb-WGA and 10 kb-dam libraries. The read-pairs that were uniq...
<p>For each bacterial genome in a set of 747 genomes, we simulated several read lengths (50 nt, 75 n...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
The graph shows the proportion of reads and test fragments at each percent difference from their ref...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
The x-axis shows the base position within a sequencing read, and the y-axis shows the average error ...
<p>(A) Percentage of small RNA reads from each genotype by size. (B) Percentages of small RNA reads ...
<p>The paternal and maternal genomes differes in 1% SNPs. The mean insert size is 250bp with 25bp st...
<p>This figure reports F1 measure varying sequencing error from 0% to 6% for 250 thousands of 120 bp...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 75 bp rea...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 120 bp re...
<p>Table reports precision varying the sequencing error from 0% to 6% for 250 thousands of 75 bp rea...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
<p>(A) shows the sequencing errors occur randomly across one read and B) shows the error rate is alm...
<p>(A), 2- to 35-kb libraries; (B), 10 kb-WGA and 10 kb-dam libraries. The read-pairs that were uniq...
<p>For each bacterial genome in a set of 747 genomes, we simulated several read lengths (50 nt, 75 n...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
The graph shows the proportion of reads and test fragments at each percent difference from their ref...
<p>The graph represents the percentage of unique best mapped reads obtained for each tool as functio...
The x-axis shows the base position within a sequencing read, and the y-axis shows the average error ...
<p>(A) Percentage of small RNA reads from each genotype by size. (B) Percentages of small RNA reads ...
<p>The paternal and maternal genomes differes in 1% SNPs. The mean insert size is 250bp with 25bp st...
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