Resources

Results per page

Selected Filters:

Next Generation Sequencing Clear Filters

Application Note

Emedgene software

18 Mar 2026

Application Note

Balanced sequencing pools through controlled amplification using AutoNorm™

9 Mar 2026

Application Note

Methods for 16S rRNA sequencing

9 Mar 2026

Application Note

AutoNorm™ of NEXTFLEX small RNA libraries using the iconPCR™ system

9 Mar 2026

Product Brochures

Microlab PuriFY

24 Feb 2026

Application Note

NEBNext UltraTM II DNA Library Prep size selection and clean-up for Illumina processed on the Microlab PuriFY

24 Feb 2026

Application Note

How to choose a molecular diagnostics supplier

A guide for early-stage molecular diagnostics companies

13 Jan 2026

Application eBook

Streamline liquid handling with automation

16 Dec 2025

White Papers

Which is the best NGS approach for CFTR diagnosis: Targeted NGS or whole exome sequencing?

17 Nov 2025

Application Note

Task-based automation in laboratory workflows

14 Nov 2025

Application Note

Fast, accurate DNA sizing with the Agilent Femto Pulse system for HIFI WGS

4 Nov 2025

Application Note

Quality control in the PacBio HiFi whole genome sequencing library preparation workflow

3 Nov 2025

White Papers

Advancing multiomics through intelligent automation

27 Oct 2025

Application Note

Automated NGS Nextera 16S metagenomic sequencing library preparation using the ASSIST PLUS pipetting robot

21 Oct 2025

Application Note

Advancing GMP compliance with HTS: Robust virus detection in high virus, low host systems

9 Sept 2025

Infographic

Have you future-proofed your cystic fibrosis testing?

8 Sept 2025

Application Note

Modernizing genetic testing for cystic fibrosis

8 Sept 2025

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 Note

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

29 Jul 2025

Case Study

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

24 Jul 2025

Application eBook

Automated liquid handling miniaturization for genomics applications

23 Jul 2025

Application Note

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

4 Jul 2025

Application Note

Decoding disease epigenetics: Innovating DNA methylation with advanced sequencing methods

2 Jul 2025

Application Note

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

1 Jul 2025

Resources

Resources Filter

Search

Selected Filters:

Emedgene software

Balanced sequencing pools through controlled amplification using AutoNorm™

Methods for 16S rRNA sequencing

AutoNorm™ of NEXTFLEX small RNA libraries using the iconPCR™ system

Microlab PuriFY

NEBNext UltraTM II DNA Library Prep size selection and clean-up for Illumina processed on the Microlab PuriFY

How to choose a molecular diagnostics supplier

Streamline liquid handling with automation

Which is the best NGS approach for CFTR diagnosis: Targeted NGS or whole exome sequencing?

Task-based automation in laboratory workflows

Fast, accurate DNA sizing with the Agilent Femto Pulse system for HIFI WGS

Quality control in the PacBio HiFi whole genome sequencing library preparation workflow

Advancing multiomics through intelligent automation

Automated NGS Nextera 16S metagenomic sequencing library preparation using the ASSIST PLUS pipetting robot

Advancing GMP compliance with HTS: Robust virus detection in high virus, low host systems

Have you future-proofed your cystic fibrosis testing?

Modernizing genetic testing for cystic fibrosis

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

Resources

Resources FilterResources Filter

Search

Selected Filters:

Emedgene software

Balanced sequencing pools through controlled amplification using AutoNorm™

Methods for 16S rRNA sequencing

AutoNorm™ of NEXTFLEX small RNA libraries using the iconPCR™ system

Microlab PuriFY

NEBNext UltraTM II DNA Library Prep size selection and clean-up for Illumina processed on the Microlab PuriFY

How to choose a molecular diagnostics supplier

Streamline liquid handling with automation

Which is the best NGS approach for CFTR diagnosis: Targeted NGS or whole exome sequencing?

Task-based automation in laboratory workflows

Fast, accurate DNA sizing with the Agilent Femto Pulse system for HIFI WGS

Quality control in the PacBio HiFi whole genome sequencing library preparation workflow

Advancing multiomics through intelligent automation

Automated NGS Nextera 16S metagenomic sequencing library preparation using the ASSIST PLUS pipetting robot

Advancing GMP compliance with HTS: Robust virus detection in high virus, low host systems

Have you future-proofed your cystic fibrosis testing?

Modernizing genetic testing for cystic fibrosis

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

Resources Filter