相关实验视频

Updated: May 11, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

单核酸多态微阵列分析揭示了马来西亚儿童B细胞前体急性淋巴细胞白血病的复制数异常和遗传异质性

Nor Soleha Mohd Dali1, Nursaedah Abdullah Aziz1, Muhamad Farid Zulkifle1

  • 1Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health, Selangor, Malaysia.

Molecular genetics & genomic medicine
|March 3, 2026
PubMed
概括

这项研究分析了马来西亚患者儿科B细胞前体急性淋巴细胞白血病 (BCP-ALL) 的基因组景观. 在SNP 6.0微阵列和MLPA中,发现了副本数异常,有助于理解BCP-ALL遗传学.

关键词:
B细胞前体急性淋巴细胞白血病.在MLPA中,我们可以使用MLPA.在SNP 6.0微阵列中.副本数量的异常情况.儿科 儿科 儿科

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Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...