Resources

Results per page

Selected Filters:

Next Generation Sequencing Clear Filters

White Papers

NGS: changing the game in CFTR analysis

20 Aug 2025

Product Brochures

Streamlining NGS library preparation with Veya's effortless automation

14 Aug 2025

Application Notes

Achieve functional knockout in up to 90% of human primary T cells

29 Jul 2025

Case Studies

Automating library preparation for rapid WGS-based diagnosis of rare diseases in the neonatal intensive care unit

24 Jul 2025

Application eBooks

Automated liquid handling miniaturization for genomics applications

23 Jul 2025

Application Notes

Comparison of DNA sample QC for NGS workflows with the Agilent Fragment Analyzer and Bioanalyzer systems

4 Jul 2025

Application Notes

Decoding disease epigenetics: Innovating DNA methylation with advanced sequencing methods

2 Jul 2025

Application Notes

NGS analysis of hereditary cancer predispositions at the Laboratory of Molecular Genetics, Jihlava Hospital

1 Jul 2025

Product Brochures

Effortless automation with VEYA

30 Jun 2025

Application Notes

Quality control of NGS libraries with daisy chains

17 Jun 2025

Application Notes

Accurately synthesize complex, linear dsDNA for in vitro transcription with Ribbon Bio’s novel DNA-assembly approach

11 Jun 2025

White Papers

Why NGS ELN deployments fail

4 Jun 2025

Application eBooks

High-throughput single cell screening for cancer research

28 May 2025

White Papers

Meeting modern demands: How NGS can help overcome thalassemia testing challenges

16 May 2025

Infographics

5 reasons to choose Devyser Thalassemia

16 May 2025

Application Notes

NGS STAR: Ready-to-run solution for NGS workflows

8 May 2025

White Papers

Challenges in laboratory detection of the α3.7 and α4.2 deletion in thalassemia

8 May 2025

Application Notes

Synthetic DNA: The fabric of modern cancer research

6 May 2025

Application Notes

Illumina® DNA Prep with Exome 2.5 Enrichment on the Revvity Sciclone™ NGSx and iQ workstations

23 Apr 2025

Product Brochures

Revvity's NGS library prep automated workstation solutions

23 Apr 2025

Application Notes

Velsera clinical genomics knowledgebase

27 Mar 2025

Application Notes

Agilent automated NGS solutions advance rare disease research at Debré Hospital

21 Mar 2025

Scientific Posters

Measuring genetics, 5-mC and 5-hmC at single-base resolution

14 Mar 2025

Infographics

Reveal the power of the 6-base genome from a single DNA molecule

14 Mar 2025

Scientific Posters

Multiomic 6-base data from cell-free DNA enhances the performance of liquid biopsy classifiers

14 Mar 2025

Resources

Resources Filter

Search

Selected Filters:

NGS: changing the game in CFTR analysis

Streamlining NGS library preparation with Veya's effortless automation

Achieve functional knockout in up to 90% of human primary T cells

Automating library preparation for rapid WGS-based diagnosis of rare diseases in the neonatal intensive care unit

Automated liquid handling miniaturization for genomics applications

Comparison of DNA sample QC for NGS workflows with the Agilent Fragment Analyzer and Bioanalyzer systems

Decoding disease epigenetics: Innovating DNA methylation with advanced sequencing methods

NGS analysis of hereditary cancer predispositions at the Laboratory of Molecular Genetics, Jihlava Hospital

Effortless automation with VEYA

Quality control of NGS libraries with daisy chains

Accurately synthesize complex, linear dsDNA for in vitro transcription with Ribbon Bio’s novel DNA-assembly approach

Why NGS ELN deployments fail

High-throughput single cell screening for cancer research

Meeting modern demands: How NGS can help overcome thalassemia testing challenges

5 reasons to choose Devyser Thalassemia

NGS STAR: Ready-to-run solution for NGS workflows

Challenges in laboratory detection of the α3.7 and α4.2 deletion in thalassemia

Synthetic DNA: The fabric of modern cancer research

Illumina® DNA Prep with Exome 2.5 Enrichment on the Revvity Sciclone™ NGSx and iQ workstations

Revvity's NGS library prep automated workstation solutions

Velsera clinical genomics knowledgebase

Agilent automated NGS solutions advance rare disease research at Debré Hospital

Measuring genetics, 5-mC and 5-hmC at single-base resolution

Reveal the power of the 6-base genome from a single DNA molecule

Multiomic 6-base data from cell-free DNA enhances the performance of liquid biopsy classifiers

Resources

Resources FilterResources Filter

Search

Selected Filters:

NGS: changing the game in CFTR analysis

Streamlining NGS library preparation with Veya's effortless automation

Achieve functional knockout in up to 90% of human primary T cells

Automating library preparation for rapid WGS-based diagnosis of rare diseases in the neonatal intensive care unit

Automated liquid handling miniaturization for genomics applications

Comparison of DNA sample QC for NGS workflows with the Agilent Fragment Analyzer and Bioanalyzer systems

Decoding disease epigenetics: Innovating DNA methylation with advanced sequencing methods

NGS analysis of hereditary cancer predispositions at the Laboratory of Molecular Genetics, Jihlava Hospital

Effortless automation with VEYA

Quality control of NGS libraries with daisy chains

Accurately synthesize complex, linear dsDNA for in vitro transcription with Ribbon Bio’s novel DNA-assembly approach

Why NGS ELN deployments fail

High-throughput single cell screening for cancer research

Meeting modern demands: How NGS can help overcome thalassemia testing challenges

5 reasons to choose Devyser Thalassemia

NGS STAR: Ready-to-run solution for NGS workflows

Challenges in laboratory detection of the α3.7 and α4.2 deletion in thalassemia

Synthetic DNA: The fabric of modern cancer research

Illumina® DNA Prep with Exome 2.5 Enrichment on the Revvity Sciclone™ NGSx and iQ workstations

Revvity's NGS library prep automated workstation solutions

Velsera clinical genomics knowledgebase

Agilent automated NGS solutions advance rare disease research at Debré Hospital

Measuring genetics, 5-mC and 5-hmC at single-base resolution

Reveal the power of the 6-base genome from a single DNA molecule

Multiomic 6-base data from cell-free DNA enhances the performance of liquid biopsy classifiers

Resources Filter