Testimonials

“We have been very happy with the Arima-HiC kit. The Arima-HiC protocol is days quicker than our previous lab’s protocol. All together, better quality data for less effort.”

– Eileen Furlong, PhD, Head of Genome Biology Unit – European Molecular Biology Laboratory (EMBL)

“Arima Genomics is an integral technology partner of the G10K consortium and Phase I of the VGP project. Arima was selected for Phase I based on the quality of their data, proven by their ability to generate reproducible and high-quality data despite variability in input sample quality and quantity. The long-range genomic interactions from Arima-HiC data is an essential component of our current strategy for the generation of chromosome-spanning reference assemblies.”

– Gene Myers, PhD, G10K Council Member and Director at Max-Planck Institute of Molecular Cell Biology and Genetics, Dresden

“When we tested Arima-HiC kit in our hands, we consistently got very high-quality libraries. Particularly, the fraction of inter-chromosomal reads is reduced.”

– Daan Noordermeer PhD, Group Leader of CNRS Chromatin Dynamics Group

“We are pleased with the ease of the Arima-HiC workflow and the improved data quality for topological domain and chromatin looping analysis. The expanded support for low input is a significant feature as it allows researchers to perform Hi-C across precious samples such as rare cell populations or clinical samples that were previously precluded from Hi-C analysis.”

– Hiruy Meharena PhD, Postdoctoral Fellow at Massachusetts Institute of Technology

“The ability of Arima-HiC kits to deliver greater insight with less sequencing cost will be critical in enabling more researchers to leverage Hi-C technology for understanding gene regulation within the three-dimensional context of the genome.”

– Changhoon Kim, PhD, Chief Technology Officer at Macrogen, Inc.

“The Arima HiC kit has worked well in our testing and provided excellent quality genome scaffolds at extremely low sequencing depths. The Arima support team have been very knowledgeable and extremely quick to respond.”

– Phil Ewels, Head of the Genomics Applications Development at NGI, SciLifeLab

“We can get a good HiC library with sufficient coverage from sequencing one HiSeq lane. With our previous methods we needed three or more lanes to get sufficient coverage.”

– Melissa Fullwood, PhD, Assistant Professor, Nanyang Technical University

“I really thought it was quite easier compared to other Hi-C methods we evaluated, and y’alls QC checks made me feel a lot better about the library preparation throughout the process.”

– Caitlin Castanada, Texas A&M