Long String Genomics
Because SIZE MATTERS
Analyzing long stretches of genetic material means leaping forward into the last frontiers in genomics.
Using such approaches will close existing gaps and unveil blindspots.
With automation solutions from Hamilton for these workflows, we aim to enable the scientific community to work at scale and make new discoveries
Specific Applications
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Automation of Long-Read Sequencing Library Preparation with PacBio SMRTbell prep kit 3.0 on Hamilton NGS STAR MOA
Advancing scientific discoveries, at scale, requires complete sequencing data, as well as suitable workflows to address high-throughput needs. Long-read sequencing technologies are quickly becoming the new gold standard to explore the full extent of genetic variation. -
High-throughput human sample prep and sequencing on PacBio Revio system
High-throughput human sample prep and sequencing on PacBio Revio system -
Automation of the QIAGEN QIAseq FX DNA Library Kit on the Hamilton NGS STARlet
Automation of the QIAGEN QIAseq FX DNA Library Kit on the Hamilton NGS STARlet Generates High-Quality Libraries for Whole-Genome Sequencing. -
Automated Isolation of High Molecular Weight (HMW) DNA from Human Blood Samples with PacBio® Nanobind® Technology on the Hamilton NIMBUS® Presto - Next Level Preparation of Extracts for Long-Read Sequencing
Long-read sequencing technology provides great potential in several clinically relevant areas of human genomics. Recent advancements allowing increased sequencing throughput and accuracy at a more affordable cost have already been made. However, the applied workflows still contain bottlenecks, especially in the extraction process steps that increase variability in HMW DNA (50 kbp -250 kbp) yield and quality, while hindering the processing of higher sample numbers. Overcoming these hurdles by robust high-throughput, automated solutions will support the growing number of large-scale population genomics studies and clinical research applications.
Advantages of Long String Genomics
Shifting BOUNDARIES
Stepping into the most advanced genomic application areas
Novel technologies in genomics have revolutionized many aspects within life science. But the journey is far from over.
The analysis of relatively short nucleic acid molecules has been of fundamental importance in research and clinical usage. However, there are limitations which leave some questions unanswered. Until now.
With the opportunity to look at larger molecules, many limitations of current standard methods can be overcome and can provide a more comprehensive picture of the genome.
Reveal the UNSEEN
High Molecular Weight (HMW) DNA Extraction for Long-Read Sequencing
Automated on NIMBUS Presto
Learn more about PacBio Long-Read Sequencing
Learn more about Hamilton NIMBUS Presto
Resolve the UNDETECTABLE
Ultra High Molecular Weight (UHMW) DNA Extraction for Optical Genome Mapping Automated on Long String STAR V
Learn more about Bionano Optical Genome Mapping
Towards a better VIEW
See what Hamilton can do if you demand the bigger picture
Learn more about Hamilton’s Long String Genomics Solutions
Additional Resources for Genomics
Check out our free Booklet about Long String GENOMICS
Explore the Hamilton Long String STAR V
Learn more about the Hamilton Microlab NIMBUS
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Whether you need a new instrument or support for one already in the lab, Hamilton is here to support you. Dedicated staff around the world are ready to respond to your request.
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