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Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

Nature biotechnology, 2013-11, Vol.31 (11), p.1023-1031

2013

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Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing

BMC genomics, 2018-01, Vol.19 (1), p.30-30, Article 30

2018

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Targeted Next-generation Sequencing of Advanced Prostate Cancer Identifies Potential Therapeutic Targets and Disease Heterogeneity

European urology, 2013-05, Vol.63 (5), p.920-926

2013

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Single-Molecule DNA Sequencing of a Viral Genome

Science (American Association for the Advancement of Science), 2008-04, Vol.320 (5872), p.106-109

2008

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Virtual terminator nucleotides for next-generation DNA sequencing

Nature methods, 2009-08, Vol.6 (8), p.593-595

2009

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Directed Evolution of DNA Polymerases for Next-Generation Sequencing

Angewandte Chemie (International ed.), 2010-08, Vol.49 (34), p.5921-5924

2010

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Electronic transport in films of colloidal CdSe nanocrystals

Physical review. B, Condensed matter, 2002-08, Vol.66 (7), Article 075339

2002

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Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

Nature biotechnology, 2016-03, Vol.34 (3), p.303-311

2016

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Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology

Nature biotechnology, 2021-09, Vol.39 (9), p.1115-1128

2021

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Abstract 397: Whole genome copy number variation analysis using a SNP-focused targeted sequencing panel for tumor analysis

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.397-397

2017

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Direct RNA sequencing

Nature (London), 2009-10, Vol.461 (7265), p.814-818

2009

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Abstract 418: Highly efficient duplex DNA tagging strategy improves accuracy of detecting ultra-low-frequency mutations through consensus read reconstruction

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.418-418

2018

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Abstract 430: Detection of low-frequency variants from highly degraded DNA samples using a novel library preparation method

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.430-430

2018

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Abstract 5598: Development and optimization of a comprehensive high-sensitivity NGS cancer assay and bioinformatics pipeline for plasma cfDNA profiling

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.5598-5598

2018

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Abstract 4742: Using 1ng of DNA to detect haplotype phasing and gene fusions from whole exome sequencing of cancer cell lines

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4742-4742

2015

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Abstract 4882: Megabase-scale phased haplotypes of genetic aberrations from whole cancer genome sequencing of primary colorectal tumors

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4882-4882

2015

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Haplotyping germline and cancer genomes using high-throughput linked-read sequencing

Nature biotechnology, 2016-02, Vol.34 (3), p.303-311

2016

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Abstract 967: Massively parallel sequencing of clinical FFPE cancer specimens enables comprehensive genomic assessment of patient eligibility for targeted therapy

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.967-967

2012

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Abstract 2279: Bringing next generation sequencing (NGS) to the clinic: Analytical validation of a comprehensive NGS-based cancer gene test

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.2279-2279

2013

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Use of next-generation sequencing (NGS) to detect a novel ALK fusion and a high frequency of other actionable alterations in colorectal cancer (CRC)

Journal of clinical oncology, 2012-05, Vol.30 (15_suppl), p.3533-3533

2012

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Reversible Charging of CdSe Nanocrystals in a Simple Solid-State Device

Advanced materials (Weinheim), 2002-08, Vol.14 (15), p.1068-1071

2002

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Directed Evolution of DNA Polymerases for Next‐Generation Sequencing

Angewandte Chemie, 2010-08, Vol.122 (34), p.6057-6060

2010

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The physics and chemistry of transport in cadmium selenide quantum dot solids

Jarosz, Mirna

2004

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Identification of new ALK and RET gene fusions from colorectal and lung cancer biopsies

Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing

Targeted Next-generation Sequencing of Advanced Prostate Cancer Identifies Potential Therapeutic Targets and Disease Heterogeneity

Single-Molecule DNA Sequencing of a Viral Genome

Virtual terminator nucleotides for next-generation DNA sequencing

Directed Evolution of DNA Polymerases for Next-Generation Sequencing

Electronic transport in films of colloidal CdSe nanocrystals

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

Emergence of Constitutively Active Estrogen Receptor-α Mutations in Pretreated Advanced Estrogen Receptor-Positive Breast Cancer

Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology

Abstract 397: Whole genome copy number variation analysis using a SNP-focused targeted sequencing panel for tumor analysis

Direct RNA sequencing

Abstract 418: Highly efficient duplex DNA tagging strategy improves accuracy of detecting ultra-low-frequency mutations through consensus read reconstruction

Abstract 430: Detection of low-frequency variants from highly degraded DNA samples using a novel library preparation method

Abstract 5598: Development and optimization of a comprehensive high-sensitivity NGS cancer assay and bioinformatics pipeline for plasma cfDNA profiling

Abstract 4742: Using 1ng of DNA to detect haplotype phasing and gene fusions from whole exome sequencing of cancer cell lines

Abstract 4882: Megabase-scale phased haplotypes of genetic aberrations from whole cancer genome sequencing of primary colorectal tumors

Haplotyping germline and cancer genomes using high-throughput linked-read sequencing

Abstract 967: Massively parallel sequencing of clinical FFPE cancer specimens enables comprehensive genomic assessment of patient eligibility for targeted therapy

Abstract 2279: Bringing next generation sequencing (NGS) to the clinic: Analytical validation of a comprehensive NGS-based cancer gene test

Use of next-generation sequencing (NGS) to detect a novel ALK fusion and a high frequency of other actionable alterations in colorectal cancer (CRC)

Reversible Charging of CdSe Nanocrystals in a Simple Solid-State Device

Directed Evolution of DNA Polymerases for Next‐Generation Sequencing

The physics and chemistry of transport in cadmium selenide quantum dot solids

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