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Node: Amp is short for amplification, and Del is for Deletion. All chromosomal aberration regions are listed at Table S3.
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2015-12-02
相关数据集
Additional file 4 of Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models
Additional file 4: Table S7. Comparison of the genes with copy number alterations in COSMIC, Ben-David et al and this study.
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Additional file 2 of Functional and population genetic features of copy number variations in two dairy cattle populations
Additional file 2: Tables S1. Summary statistics for CNVs in ARS-UCD1.2 and UMD3.1. Table S2. Detailed features of CNVRs on autosomes identified in this study. Table S3. Chromosome-wide CNVR coverage
Figshare2020-01-28 更新40
Drosophila salivary gland imaginal ring tumor single cell DNA copy number variation (CNV)
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Table_13_Pan-Genomic Study of Mycobacterium tuberculosis Reflecting the Primary/Secondary Genes, Generality/Individuality, and the Interconversion Through Copy Number Variations.DOCX
Tuberculosis (TB) has surpassed HIV as the leading infectious disease killer worldwide since 2014. The main pathogen, Mycobacterium tuberculosis (Mtb), contains ~4,000 genes that account for ~90% of t
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Shallow whole genome sequencing of biopsies from retinoblastoma tumors in chimeric murine knockout double mice (pRb-p130 and pRb-p107 knockouts) to identify secondary alterations that drive oncogenesis.
Several murine retinoblastoma models have been generated by deleting the genes encoding for retinoblastoma susceptibility protein pRb and one of its family members p107 or p130. In Rb-/-p107-/- retino
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