GenomicsGenomicsPeer-reviewed journal article
Hi-C detects novel structural variants in HL-60 and HL-60/S4 cell lines
Elsie C. JacobsoniD, Ralph Stefan GrandiD, Jo Kate PerryiD, Mark Hedley VickersiD, Ada L. OlinsiD, Donald E. OlinsiD, Justin Martin O'SullivaniD
Abstract
Cancer cell lines often have large structural variants (SVs) that evolve over time. There are many reported differences in large scale SVs between HL-60 and HL-60/S4, cell lines derived from the same acute promyelocytic leukemia sample. However, the stability and variability of inter- and intra-chromosomal SVs between different sources is unknown. Here, we used Hi-C and RNA-seq to identify and compare large SVs in HL-60 and HL-60/S4 cell lines.\n\nComparisons with previously reported karyotypes identified two non-canonical SVs in HL-60. Ten previously unreported SVs were identified in HL-60/S4. The unreported SVs were generally small enough to be plausibly undetected with traditional karyotyping methods. An expansion centered on MYC was found in a novel genomic location in HL-60. The HL-60 cell line has more within-line structural variation than the HL-60/S4 derivative cell line.\n\nHL-60 and HL-60/S4 karyotypes are generally consistent with the current literature, with some exceptions. Hic_breakfinder is an effective tool for identifying all SVs, but intra-chromosomal SVs are less reliably detected across different samples. The orientation of SV patterns, and strandedness of gene fusions, allowed us to differentiate inversions from other forms of intra-chromosomal SV. Visual inspection of Hi-C heatmap patterns allow further characterization of SVs without additional methods, although orthogonal information such as gene fusions contribute to the characterization.
- organism: human
- assay: Hi-C
- assay: bulk RNA-seq
- research focus: variant calling
- research focus: benchmarking
- approach: statistical model
- approach: experimental assay
- Citations
- 23
- FWCI
- 2.40
- Field percentile
- top 11%
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