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Hi-C detects novel structural variants in HL-60 and HL-60/S4 cell lines

机译:HI-C检测HL-60和HL-60 / S4细胞系中的新型结构变体

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摘要

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, two cell lines derived from the same acute myeloid leukemia sample. However, the stability and variability of inter- and infra-chromosomal structural variants between different sources of the same cell line 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. Comparisons with previously published karyotypes identified novel SVs in both cell lines. Hi-C was used to characterize the known expansion centered on the MYC locus. The MYC expansion was integrated into known locations in HL-60/S4, and a novel location (chr4) in HL-60. The HL-60 cell line has more within-line structural variation than the HL-60/S4 derivative cell line. Collectively we demonstrate the usefulness of Hi-C and with RNA-seq data for the identification and characterization of SVs.
机译:癌细胞系通常具有大规模的结构变体(SVS)随时间而发展。 HL-60和HL-60 / S4之间的大规模SVS有许多报道的差异,两种细胞系来自同一急性髓性白血病样品。 然而,相同细胞系的不同来源之间的稳定性和染色体结构变体的稳定性和可变性是未知的。 在这里,我们使用HI-C和RNA-SEQ来识别和比较HL-60和HL-60 / S4细胞系中的大型SV。 与以前公布的核型的比较鉴定了两种细胞系中的新型SV。 HI-C用于表征以MYC基因座为中心的已知膨胀。 将Myc扩展集成到HL-60 / S4中的已知位置,以及HL-60中的新型位置(CHR4)。 HL-60细胞系具有比HL-60 / S4衍生物细胞系更多的线结构变化。 统称我们展示了Hi-C的有用性以及RNA-SEQ数据,用于鉴定和表征SVS。

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