<p>The ten most common nucleotide V3 sequences from samples 10–172, 10–176, and 10–180 -obtained with each of the four NGS platforms (454™, Illumina®, PacBio®, and Ion Torrent™)- were aligned against the respective population (sanger) sequence and analyzed as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0049602#pone-0049602-g004" target="_blank">Figure 4</a> legend.</p
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic va...
<p>The ten most common nucleotide V3 sequences from samples 10–75, 10–80, and 10–91 -obtained with e...
<p>The heights of the bars represent the combined frequency of V3 variants detected by the NGS platf...
For the robust practice of genomic medicine, sequencing results must be compatible, regardless of th...
<div><p>For the robust practice of genomic medicine, sequencing results must be compatible, regardle...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
<p>(A) Nucleotide minority variants categorized by platform (Illumina vs. 454) and whether the minor...
BACKGROUND: Next Generation Sequencing (NGS) is the fundament of various studies, providing insights...
Objectives: To compare next-generation sequencing (NGS) plafforms with mutation-specific analysis pl...
Massively parallel sequencing (MPS) has revolutionised clinical genetics and research within human g...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic va...
Background: Along with the improvement of high throughput sequencing technologies, the genetics comm...
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic va...
<p>The ten most common nucleotide V3 sequences from samples 10–75, 10–80, and 10–91 -obtained with e...
<p>The heights of the bars represent the combined frequency of V3 variants detected by the NGS platf...
For the robust practice of genomic medicine, sequencing results must be compatible, regardless of th...
<div><p>For the robust practice of genomic medicine, sequencing results must be compatible, regardle...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
<p>(A) Nucleotide minority variants categorized by platform (Illumina vs. 454) and whether the minor...
BACKGROUND: Next Generation Sequencing (NGS) is the fundament of various studies, providing insights...
Objectives: To compare next-generation sequencing (NGS) plafforms with mutation-specific analysis pl...
Massively parallel sequencing (MPS) has revolutionised clinical genetics and research within human g...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic va...
Background: Along with the improvement of high throughput sequencing technologies, the genetics comm...
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
To obtain reliable variant results, the accuracy of sequence alignment, consensus calling and varian...
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic va...