• Archiving the log files allows you to move the log files to another location for analysis, storage, or deletion purposes.

    通过对日志文件进行归档,可以将日志文件移动到另外一个位置进行分析、存储或删除。

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  • Results: All the 4 rats were involved in the analysis of results without deletion.

    结果:进入统计分析的大鼠保持为4只,无缺失值。

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  • To analyze deletion of chromosome 16 by microsatellite analysis.

    应用微卫星序列分析16号染色体缺失情况。

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  • The author summarizes the related private and public law system in our country, affirms their success, and then conducts a comprehensive analysis of its deletion.

    在肯定我国法律保护成绩的同时,亦重点对制度缺失进行了分析。

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  • Third, the analysis of the FAT32 file deletion principle, and to achieve the restoration of the document accidental delete.

    第三,分析了FAT32文件的删除原理,编码实现了文件误删除的恢复。

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  • Experiments and analysis show that this method is robust not only to various conventional attacks, but also to re-frame, frame cropping, frame deletion and other video-specific attacks.

    实验和分析表明,该方法不仅对各种常规攻击鲁棒,而且对帧重组、帧内裁剪和帧删除等视频特有攻击表现出强的鲁棒性。

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  • It can realize not only the data manipulating functions such as browsing, query, copy, output, adding, deletion, modification and renewing, but also spatiotemporal analysis.

    系统具备了对数据的浏览、查询、复制、输出以及增加、删减、修改、更新等功能,还能对数据进行时空分析。

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  • This is a process of confirmation, analysis and deletion for getting an optimal method.

    这是一个确定,分析和删除的过程,以找到最佳方案。

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  • The gene overlapping(ATGA) is widespread in streptomycetes, making it difficult to perform in-frame deletion or replacement for functional analysis of target genes.

    链霉菌基因组中常见连续两个基因重叠的现象(如ATGA),这为基因的同框敲除或取代研究带来很大困扰。

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  • Using MLPA analysis, we detected two large genomic rearrangements in three families, a deletion of exons 21 and 22, and a rare deletion of a whole BRCA1 gene.

    使用多重连接依赖式探针扩增(MLPA),我们在三个家族中检测两个大的基因组重排,检测21和22外显子和整条BRCA1基因上的一个罕见缺失。

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  • Using MLPA analysis, we detected two large genomic rearrangements in three families, a deletion of exons 21 and 22, and a rare deletion of a whole BRCA1 gene.

    使用多重连接依赖式探针扩增(MLPA),我们在三个家族中检测两个大的基因组重排,检测21和22外显子和整条BRCA1基因上的一个罕见缺失。

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