Additional file 3 of Impact of extracellular matrix stiffness on genomic heterogeneity in MYCN-amplified neuroblastoma cell line
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Additional file 3: Table S2: Genomic variants detected by next generation sequencing (NGS) in the sequenced samples from (A) SK-N-BE(2) cells or (B) SH-SY5Y cells, filtered by mean allelic frequencies equal to or over 0.1, and a coverage equal to or over 100x. XenofilteR and Disambiguate software were applied to remove variants from mice genome and SW10 cells. (C) Genomic regions included in NB-mechanopanel.
创建时间：
2020-10-28
