Development and Validation of StrataNGS, a Multiplex PCR, Semiconductor Sequencing-Based Comprehensive Genomic Profiling Test
Despite widespread use in targeted tumor testing, multiplex PCR/semiconductor (Ion Torrent) sequencing-based assessment of all comprehensive genomic profiling (CGP) variant classes has been limited. Herein, we describe the development and validation of StrataNGS, a 429-gene, multiplex PCR/semiconduc...
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Veröffentlicht in: | The Journal of molecular diagnostics : JMD 2021-11, Vol.23 (11), p.1515-1533 |
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creator | Tomlins, Scott A. Hovelson, Daniel H. Harms, Paul Drewery, Stephanie Falkner, Jayson Fischer, Andrew Hipp, Jennifer Kwiatkowski, Kat Lazo de la Vega, Lorena Mitchell, Khalis Reeder, Travis Siddiqui, Javed Vakil, Hana Johnson, D. Bryan Rhodes, Daniel R. |
description | Despite widespread use in targeted tumor testing, multiplex PCR/semiconductor (Ion Torrent) sequencing-based assessment of all comprehensive genomic profiling (CGP) variant classes has been limited. Herein, we describe the development and validation of StrataNGS, a 429-gene, multiplex PCR/semiconductor sequencing-based CGP laboratory-developed test performed on co-isolated DNA and RNA from formalin-fixed, paraffin-embedded tumor specimens with ≥2 mm2 tumor surface area. Validation was performed in accordance with MolDX CGP validation guidelines using 1986 clinical formalin-fixed, paraffin-embedded samples and an in-house developed optimized bioinformatics pipeline. Across CGP variant classes, accuracy ranged from 0.945 for tumor mutational burden (TMB) status to >0.999 for mutations and gene fusions, positive predictive value ranged from 0.915 for TMB status to 1.00 for gene fusions, and reproducibility ranged from 0.998 for copy number alterations to 1.00 for splice variants and insertions/deletions. StrataNGS TMB estimates were highly correlated to those from whole exome– or FoundationOne CDx–determined TMB (Pearson r = 0.998 and 0.960, respectively); TMB reproducibility was 0.996 (concordance correlation coefficient). Limit of detection for all variant classes was |
doi_str_mv | 10.1016/j.jmoldx.2021.08.005 |
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Bryan ; Rhodes, Daniel R.</creator><creatorcontrib>Tomlins, Scott A. ; Hovelson, Daniel H. ; Harms, Paul ; Drewery, Stephanie ; Falkner, Jayson ; Fischer, Andrew ; Hipp, Jennifer ; Kwiatkowski, Kat ; Lazo de la Vega, Lorena ; Mitchell, Khalis ; Reeder, Travis ; Siddiqui, Javed ; Vakil, Hana ; Johnson, D. Bryan ; Rhodes, Daniel R.</creatorcontrib><description>Despite widespread use in targeted tumor testing, multiplex PCR/semiconductor (Ion Torrent) sequencing-based assessment of all comprehensive genomic profiling (CGP) variant classes has been limited. Herein, we describe the development and validation of StrataNGS, a 429-gene, multiplex PCR/semiconductor sequencing-based CGP laboratory-developed test performed on co-isolated DNA and RNA from formalin-fixed, paraffin-embedded tumor specimens with ≥2 mm2 tumor surface area. Validation was performed in accordance with MolDX CGP validation guidelines using 1986 clinical formalin-fixed, paraffin-embedded samples and an in-house developed optimized bioinformatics pipeline. Across CGP variant classes, accuracy ranged from 0.945 for tumor mutational burden (TMB) status to >0.999 for mutations and gene fusions, positive predictive value ranged from 0.915 for TMB status to 1.00 for gene fusions, and reproducibility ranged from 0.998 for copy number alterations to 1.00 for splice variants and insertions/deletions. StrataNGS TMB estimates were highly correlated to those from whole exome– or FoundationOne CDx–determined TMB (Pearson r = 0.998 and 0.960, respectively); TMB reproducibility was 0.996 (concordance correlation coefficient). Limit of detection for all variant classes was <20% tumor content. 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Bryan</creatorcontrib><creatorcontrib>Rhodes, Daniel R.</creatorcontrib><title>Development and Validation of StrataNGS, a Multiplex PCR, Semiconductor Sequencing-Based Comprehensive Genomic Profiling Test</title><title>The Journal of molecular diagnostics : JMD</title><addtitle>J Mol Diagn</addtitle><description>Despite widespread use in targeted tumor testing, multiplex PCR/semiconductor (Ion Torrent) sequencing-based assessment of all comprehensive genomic profiling (CGP) variant classes has been limited. Herein, we describe the development and validation of StrataNGS, a 429-gene, multiplex PCR/semiconductor sequencing-based CGP laboratory-developed test performed on co-isolated DNA and RNA from formalin-fixed, paraffin-embedded tumor specimens with ≥2 mm2 tumor surface area. Validation was performed in accordance with MolDX CGP validation guidelines using 1986 clinical formalin-fixed, paraffin-embedded samples and an in-house developed optimized bioinformatics pipeline. 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Bryan</au><au>Rhodes, Daniel R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Validation of StrataNGS, a Multiplex PCR, Semiconductor Sequencing-Based Comprehensive Genomic Profiling Test</atitle><jtitle>The Journal of molecular diagnostics : JMD</jtitle><addtitle>J Mol Diagn</addtitle><date>2021-11</date><risdate>2021</risdate><volume>23</volume><issue>11</issue><spage>1515</spage><epage>1533</epage><pages>1515-1533</pages><issn>1525-1578</issn><eissn>1943-7811</eissn><abstract>Despite widespread use in targeted tumor testing, multiplex PCR/semiconductor (Ion Torrent) sequencing-based assessment of all comprehensive genomic profiling (CGP) variant classes has been limited. Herein, we describe the development and validation of StrataNGS, a 429-gene, multiplex PCR/semiconductor sequencing-based CGP laboratory-developed test performed on co-isolated DNA and RNA from formalin-fixed, paraffin-embedded tumor specimens with ≥2 mm2 tumor surface area. Validation was performed in accordance with MolDX CGP validation guidelines using 1986 clinical formalin-fixed, paraffin-embedded samples and an in-house developed optimized bioinformatics pipeline. Across CGP variant classes, accuracy ranged from 0.945 for tumor mutational burden (TMB) status to >0.999 for mutations and gene fusions, positive predictive value ranged from 0.915 for TMB status to 1.00 for gene fusions, and reproducibility ranged from 0.998 for copy number alterations to 1.00 for splice variants and insertions/deletions. StrataNGS TMB estimates were highly correlated to those from whole exome– or FoundationOne CDx–determined TMB (Pearson r = 0.998 and 0.960, respectively); TMB reproducibility was 0.996 (concordance correlation coefficient). Limit of detection for all variant classes was <20% tumor content. Together, we demonstrate that multiplex PCR/semiconductor sequencing-based tumor tissue CGP is feasible using optimized bioinformatic approaches described herein.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34454112</pmid><doi>10.1016/j.jmoldx.2021.08.005</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0001-7755-0877</orcidid><orcidid>https://orcid.org/0000-0001-8742-4727</orcidid><orcidid>https://orcid.org/0000-0003-3609-0098</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers, Tumor - genetics Data Accuracy DNA Copy Number Variations Exome Feasibility Studies Gene Fusion Genome, Human Genomics - methods High-Throughput Nucleotide Sequencing - methods Humans Limit of Detection Microsatellite Instability Multiplex Polymerase Chain Reaction - methods Neoplasms - genetics Neoplasms - pathology Reproducibility of Results Sequence Analysis, DNA - methods Sequence Analysis, RNA - methods |
title | Development and Validation of StrataNGS, a Multiplex PCR, Semiconductor Sequencing-Based Comprehensive Genomic Profiling Test |
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