bioRxiv · 10.1101/669275
BAMscale: quantification of DNA sequencing peaks and generation of scaled coverage tracks
Abstract
BAMscale is a one-step tool that processes DNA sequencing datasets from chromatin binding (ChIP-seq) and chromatin state changes (ATAC-seq, END-seq) experiments to DNA replication data (OK-seq, NS-seq and replication timing). The outputs include normalized peak scores in text format and scaled coverage tracks (BigWig) which are directly accessible to data visualization programs. BAMscale (available at https://github.com/ncbi/BAMscale) effectively processes large sequencing datasets (~100Gb size) in minutes, outperforming currently available tools.
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Pongor, L. S., Gross, J. M., Vera Alvarez, R., Murai, J., Jang, S.-M., Zhang, H., Redon, C., Fu, H., Huang, S.-Y., Thakur, B., Baris, A., Marino-Ramirez, L., Landsman, D., Mirit, A. I., Pommier, Y.. 2019-06-13. BAMscale: quantification of DNA sequencing peaks and generation of scaled coverage tracks. https://doi.org/10.1101/669275
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