A wild-type plasma sample was sequenced using a 19-amplicon panel with both methods, and the FPR plotted per base position. Amplicon sequencing (grey) has an average FPR of 1.2 x 10−4 errors per base, compared to Pro-Seq (green), which had an average FPR of 1.1 x 10−6 errors per base (a known SNP at panel position 237 is ignored for FPR calculations).</p
Despite the central role of quantitative PCR (qPCR) in the quantification of mRNA transcripts, most ...
Next-generation sequencing technologies enable the rapid cost-effective production of sequence data....
<p>The MC was sequenced by different centers on both 3730 and 454 platforms. Each sequencing trial i...
<p>(A) A density plot of the expected distribution of fragment lengths, with peaks at 124 and 142 bp...
<p><b>A.</b> Amplicon performance grading did not significantly differ between the two panels. Colum...
International audienceBackground: The rapid evolution of 454 GS-FLX sequencing technology has not be...
<p><b>A:</b> B panel; <b>B:</b> T panel. Read ratios for all amplicons for matched samples sorted pe...
<p>For all four experiments, the total number of reads obtained and those overlapping amino acids 10...
Objective: Next-generation sequencing (NGS) is the next best thing for oncology biomarker testing in...
Massively parallel sequencing (MPS) is a powerful tool transforming DNA analysis in multiple fields ...
<p>The ‘Custom’ protocol refers to the modified RNA-Seq method used in this study to create larger i...
High-fidelity 'proofreading' polymerases are often used in library construction for next-generation ...
<p>Mapped reads, reads on target, mean coverage, and mean read length of the sequenced sample sets (...
Use of next-generation sequencing to detect somatic variants in DNA extracted from formalin-fixed, p...
<div><p>Massively parallel sequencing (MPS) is a powerful tool transforming DNA analysis in multiple...
Despite the central role of quantitative PCR (qPCR) in the quantification of mRNA transcripts, most ...
Next-generation sequencing technologies enable the rapid cost-effective production of sequence data....
<p>The MC was sequenced by different centers on both 3730 and 454 platforms. Each sequencing trial i...
<p>(A) A density plot of the expected distribution of fragment lengths, with peaks at 124 and 142 bp...
<p><b>A.</b> Amplicon performance grading did not significantly differ between the two panels. Colum...
International audienceBackground: The rapid evolution of 454 GS-FLX sequencing technology has not be...
<p><b>A:</b> B panel; <b>B:</b> T panel. Read ratios for all amplicons for matched samples sorted pe...
<p>For all four experiments, the total number of reads obtained and those overlapping amino acids 10...
Objective: Next-generation sequencing (NGS) is the next best thing for oncology biomarker testing in...
Massively parallel sequencing (MPS) is a powerful tool transforming DNA analysis in multiple fields ...
<p>The ‘Custom’ protocol refers to the modified RNA-Seq method used in this study to create larger i...
High-fidelity 'proofreading' polymerases are often used in library construction for next-generation ...
<p>Mapped reads, reads on target, mean coverage, and mean read length of the sequenced sample sets (...
Use of next-generation sequencing to detect somatic variants in DNA extracted from formalin-fixed, p...
<div><p>Massively parallel sequencing (MPS) is a powerful tool transforming DNA analysis in multiple...
Despite the central role of quantitative PCR (qPCR) in the quantification of mRNA transcripts, most ...
Next-generation sequencing technologies enable the rapid cost-effective production of sequence data....
<p>The MC was sequenced by different centers on both 3730 and 454 platforms. Each sequencing trial i...