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Long-read sequencing vs short-read sequencing

Different sequencing platforms use a variety of read lengths. Both short-read sequencing and long-read sequencing have their own benefits and […]

FoG 2020 Presentation Christopher Watson, University of Leeds: Clinical applications of long-read sequencing

Dr Watson is a HCPC registered Clinical Scientist leading NHS research and development activities in the Translational Genomics Unit (a […]

FoG 2020 Presentation Alba Sanchis-Juan: Long-read Whole Genome Sequencing of Clinical Samples

Alba studied Biochemistry and Biomedicine and did her PhD in Biotechnology at University of Valencia, Spain. She currently works at […]

Which NGS DNA Library Prep Kit should you choose?

This feature was put together using content from Chapter 2 of the 2024 Sequencing Buyer’s Guide. For an in depth […]

The Sequencing Buyer’s Guide: 6th Edition

Next generation sequencing, both short reads and long reads, is undergoing a second wave of exciting developments. New short-read platforms […]

The Latest Developments in Sequencing Technologies

This feature was put together using content from Chapter 3 and Chapter 9 of the 2024 Sequencing Buyer’s Guide. For […]

How-to: NGS Quality Control

Check out the new 2024 edition of our Sequencing Buyer’s Guide Thanks to the introduction of high-throughput next generation sequencing […]

Conservation Genomics: Saving a Million Species from Extinction 

Conservation genomics is a new and emerging field of research that harnesses the power of genomic technology to preserve species, […]

New Commercial Developments in Single-cell Sequencing

This feature on single-cell sequencing technology is adapted from parts of Chapters 1 & 2 of the 2023 Spatial and […]

Capturing the complexity of single-cell interactions

‘Capturing the complexity of single-cell interactions’ – Written by Charlotte Harrison, Science Writer. Single-cell and spatial genomics approaches generate high-dimensional […]