The eight most frequent patterns of MM correction were identified by analyzing all reads for each of 96 colonies per library and assigning them a genotype based on the most frequently observed read(s); see Material and Methods for details. Statistics for the number of reads per colony: mean ± sd = 186 ± 112; Interquartile range (IQR) = 111–241; Range = 7–1139. Only genotypes that appear more than 9 times for at least one of the strains are shown; complete results are shown in S8 and S9 Figs.</p
<p>Strains are shown in white boxes, mutagenesis treatments are shown in red boxes, and SNPs are sho...
AbstractA simple method of inferring the genotyping error rate of SNP arrays and similar high-throug...
a<p>A total of 10,000 permutations were performed using Haploview v4.2 to obtain a measure of signif...
<p>(A) shows the ratios of singletons to doubletons observed in the X-QTL data and for different cla...
<p>Each probe set (i.e. collection of all probes hybridizing to USA300 genes) is represented by a si...
We typed 147 simple sequence length polymorphisms in the SWXJ recombinant inbred (RI) strain set spa...
AbstractWe performed an analysis of global microsatellite variation on the two kindreds sequenced at...
Left: the six columns from the chart correspond to the repair of each MM except MM2 and represent th...
Sanger sequencing analysis of SSA progeny showing the polymerase δ effect on mismatch correction dur...
Linkage between markers and genes that affect a phenotype of interest may be determined by examining...
<p>SNPs were found by comparing mapping results of the strains to the <i>L</i>. <i>infantum</i> JPCM...
<p>Replication analysis, in independent ASPs, of the three Chromosomes (3, 11, and 17) most strongly...
Structural variants (SVs) and short tandem repeats (STRs) are important sources of genetic diversity...
At least 40 human diseases are associated with repeat expansions; yet, the mutational origin and ins...
Although it is clear that errors in genotyping data can lead to severe errors in linkage analysis, t...
<p>Strains are shown in white boxes, mutagenesis treatments are shown in red boxes, and SNPs are sho...
AbstractA simple method of inferring the genotyping error rate of SNP arrays and similar high-throug...
a<p>A total of 10,000 permutations were performed using Haploview v4.2 to obtain a measure of signif...
<p>(A) shows the ratios of singletons to doubletons observed in the X-QTL data and for different cla...
<p>Each probe set (i.e. collection of all probes hybridizing to USA300 genes) is represented by a si...
We typed 147 simple sequence length polymorphisms in the SWXJ recombinant inbred (RI) strain set spa...
AbstractWe performed an analysis of global microsatellite variation on the two kindreds sequenced at...
Left: the six columns from the chart correspond to the repair of each MM except MM2 and represent th...
Sanger sequencing analysis of SSA progeny showing the polymerase δ effect on mismatch correction dur...
Linkage between markers and genes that affect a phenotype of interest may be determined by examining...
<p>SNPs were found by comparing mapping results of the strains to the <i>L</i>. <i>infantum</i> JPCM...
<p>Replication analysis, in independent ASPs, of the three Chromosomes (3, 11, and 17) most strongly...
Structural variants (SVs) and short tandem repeats (STRs) are important sources of genetic diversity...
At least 40 human diseases are associated with repeat expansions; yet, the mutational origin and ins...
Although it is clear that errors in genotyping data can lead to severe errors in linkage analysis, t...
<p>Strains are shown in white boxes, mutagenesis treatments are shown in red boxes, and SNPs are sho...
AbstractA simple method of inferring the genotyping error rate of SNP arrays and similar high-throug...
a<p>A total of 10,000 permutations were performed using Haploview v4.2 to obtain a measure of signif...