Allele-Specific Copy Number Variation detection in tumor genomes with high-throughput sequencing dat

来源 :第六届全国生物信息学与系统生物学学术大会暨国际生物信息学前沿研讨会 | 被引量 : 0次 | 上传用户:liongliong518
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  Background: Cancer genomes are evolved from normal genomes by accumulating somatic mutations.Previous researches show that tumor genomes may preferentially have copy number variations at one allele of a heterozygous SNP locus of the normal genome, and this is called allele specific copy number variation (ASCNV).ASCNVs may confer critical survival advantage to tumor cells, and therefore studies on ASCNVs can give insightful information about tumor progression.
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