<p>Correct discordant read pairs are expressed relative to all reads mapped across the same breakpoint, as a function of the length of the repeat (relative to the length of the template) and the identity between the copies (relative to the read length). Data from all 14 simulated paired-end sequencing experiments are used. Cells may have different standard errors, due to differences in the total number of reads used to calculate the proportion of discordant pairs in each situation.</p
A) Read numbers per sample and B) percentage of reads mapped to the reference genome. C) Comparison ...
<p>Datasets Ex3 and Ex4 contain markers scored with errors and missing data, with different distribu...
<p>Results of comparisons of discordance p-values ( transformed) between L262 and base-subsampled L7...
<div><p>Frequency in 1,000 trials plotted against percentage divergence.</p><p>(A) All alleles (repr...
<p>The fraction of de-noised sequence reads with highest pairwise alignment scores to the indicated ...
<p>(A) shows the sequencing errors occur randomly across one read and B) shows the error rate is alm...
<p>Note: 30 cycles of PCR with 1000 copies of each template.</p><p>Comparison of recombination frequ...
<p>The correct positions of reads A, B, C and D are shown. (b) A “fork” in the overlaps. (c) a scena...
<p>Pairwise discordance rates are shown, for a first-pass test of all 576 samples.</p
The x-axis shows the base position within a sequencing read, and the y-axis shows the average error ...
<p>Barplots of (A) the number of total reads (i.e. number of reads of F3- and F5-tagged paired reads...
<p>The total number of reads used in the analysis affects different-sample comparisons, but not same...
<p>Numbers noted on each bar represent the number of samples that were or were not confirmed by sequ...
<p>R1 = sequencing experiment 1, R2 = sequencing experiment 2, R3 = sequencing experiment 3.</p><p>T...
<p>A. Sequencing coverage depth per marker pair. B. Frequency of discordant vs. concordant marker pa...
A) Read numbers per sample and B) percentage of reads mapped to the reference genome. C) Comparison ...
<p>Datasets Ex3 and Ex4 contain markers scored with errors and missing data, with different distribu...
<p>Results of comparisons of discordance p-values ( transformed) between L262 and base-subsampled L7...
<div><p>Frequency in 1,000 trials plotted against percentage divergence.</p><p>(A) All alleles (repr...
<p>The fraction of de-noised sequence reads with highest pairwise alignment scores to the indicated ...
<p>(A) shows the sequencing errors occur randomly across one read and B) shows the error rate is alm...
<p>Note: 30 cycles of PCR with 1000 copies of each template.</p><p>Comparison of recombination frequ...
<p>The correct positions of reads A, B, C and D are shown. (b) A “fork” in the overlaps. (c) a scena...
<p>Pairwise discordance rates are shown, for a first-pass test of all 576 samples.</p
The x-axis shows the base position within a sequencing read, and the y-axis shows the average error ...
<p>Barplots of (A) the number of total reads (i.e. number of reads of F3- and F5-tagged paired reads...
<p>The total number of reads used in the analysis affects different-sample comparisons, but not same...
<p>Numbers noted on each bar represent the number of samples that were or were not confirmed by sequ...
<p>R1 = sequencing experiment 1, R2 = sequencing experiment 2, R3 = sequencing experiment 3.</p><p>T...
<p>A. Sequencing coverage depth per marker pair. B. Frequency of discordant vs. concordant marker pa...
A) Read numbers per sample and B) percentage of reads mapped to the reference genome. C) Comparison ...
<p>Datasets Ex3 and Ex4 contain markers scored with errors and missing data, with different distribu...
<p>Results of comparisons of discordance p-values ( transformed) between L262 and base-subsampled L7...