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SEQU-INTO: Early detection of impurities contamination and off-targets (ICOs) in long read/MinION sequencing

机译:顺序进入:在长读/碎肠测序中早期检测杂质污染和偏离目标(ICOS)

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摘要

The MinION sequencer by Oxford Nanopore Technologies turns DNA and RNA sequencing into a routine task in biology laboratories or in field research. For downstream analysis it is required to have a sufficient amount of target reads. Especially prokaryotic or bacteriophagic sequencing samples can contain a significant amount of off-target sequences in the processed sample, stemming from human DNA/RNA contamination, insufficient rRNA depletion, or remaining DNA/RNA from other organisms (e.g. host organism from bacteriophage cultivation). Such impurity, contamination and off-targets (ICOs) block read capacity, requiring to sequence deeper. In comparison to second-generation sequencing, MinION sequencing allows to reuse its chip after a (partial) run. This allows further usage of the same chip with more sample, even after adjusting the library preparation to reduce ICOs. The earlier a sample’s ICOs are detected, the better the sequencing chip can be conserved for future use. Here we present sequ-into, a low-resource and user-friendly cross-platform tool to detect ICO sequences from a predefined ICO database in samples early during a MinION sequencing run. The data provided by sequ-into empowers the user to quickly take action to preserve sample material and chip capacity. sequ-into is available from https://github.com/mjoppich/sequ-into
机译:牛津纳米孔技术的碎序列序列将DNA和RNA测序转变为生物实验室的常规任务或现场研究。对于下游分析,需要足够量的目标读数。特别是原核或噬菌体测序样品可含有大量的加工样品中的脱靶序列,源于人DNA / RNA污染,不足的RRNA耗尽或来自其他生物的DNA / RNA(例如,来自噬菌体培养的宿主生物)。这种杂质,污染和偏离目标(ICOS)块读取容量,需要序列更深。与第二代测序相比,甲型测序允许在(部分)运行之后重用其芯片。这允许在调整文库准备以减少ICOS之后,进一步使用更多的样品。检测到较早的样本的ICO,可以节省序列芯片以供将来使用越好。在这里,我们将SEDING,低资源和用户友好的跨平台工具呈现出在碎钟排序运行期间早期从预定义的ICO数据库中检测ICO序列。由SED-empowers提供的数据提供了用户快速采取行动以保护样品和芯片容量。 shoud-in可从https://github.com/mjoppich/seque-into获得

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