Supporting data for "Hi-C chromosome conformation capture sequencing of avian genomes using the BGISEQ-500 platform"

Hi-C experiments couple DNA-DNA proximity with next-generation sequencing to yield an unbiased description of genome-wide interactions. Previous methods describing Hi-C experiments have focused on the industry-standard, Illumina sequencing. With new next-generation sequencing platforms such as BGISEQ-500 becoming more widely available, protocol adaptations to fit platform-specific requirements are useful to give increased choice to researchers who routinely generate sequencing data. We describe an <em>in-situ </em> Hi-C protocol adapted to be compatible with the the BGISEQ-500 high-throughput sequencing platform. Using zebra finch (<em>Taeniopygia guttata</em>) as a biological sample, we demonstrate how Hi-C libraries can be constructed to generate informative data using the BGISEQ-500 platform, following circularization and DNA nanoball generation. Our protocol is a modification of an Illumina-compatible method, based around blunt-end ligations in library construction, using un-barcoded, distally overhanging double-stranded adapters, followed by amplification using indexed primers. The resulting libraries are ready for circularization and subsequent sequencing on the BGISEQ series of platforms, and yield data similar to what can be expected using Illumina-compatible approaches. Our straightforward modification to an Illumina-compatible <em>in-situ</em> Hi-C protocol enables data generation on the BGISEQ series of platforms, thus expanding the options available for researchers who wish to utilize the powerful Hi-C techniques in their research.