Medscape22 天
Detection of Copy Number Alterations in Acute Myeloid Leukemia and Myelodysplastic Syndromes
Validation: custom CGH array (NimbleGen) for all reported CNAs Paired normal DNA (skin; 86) 201 acquired CNAs CNAs detected by SNP array but not MC in 40% patients CN-LOH in 8% patients (6 out of ...
Medscape12 年
Detection of Copy Number Alterations in Acute Myeloid Leukemia and Myelodysplastic Syndromes
Validation: custom CGH array (NimbleGen) for all reported CNAs Paired normal DNA (skin; 86) 201 acquired CNAs CNAs detected by SNP array but not MC in 40% patients CN-LOH in 8% patients (6 out of ...
Nature5 年
Finding copy-number variants
Several studies evaluate high-density single-nucleotide polymorphism (SNP) arrays for the detection of copy-number variations in human genomes. Many debilitating diseases have complex genetic ...