Repliscan: a tool for classifying replication timing regions

Replication timing experiments that use label incorporation and high throughput sequencing produce peaked data similar to ChIP-Seq experiments. However, the differences in experimental design, coverage density, and possible results make traditional ChIP-Seq analysis methods inappropriate for use wit...

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Veröffentlicht in:BMC bioinformatics 2017-08, Vol.18 (1), p.362-362, Article 362
Hauptverfasser: Zynda, Gregory J, Song, Jawon, Concia, Lorenzo, Wear, Emily E, Hanley-Bowdoin, Linda, Thompson, William F, Vaughn, Matthew W
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Sprache:eng
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Zusammenfassung:Replication timing experiments that use label incorporation and high throughput sequencing produce peaked data similar to ChIP-Seq experiments. However, the differences in experimental design, coverage density, and possible results make traditional ChIP-Seq analysis methods inappropriate for use with replication timing. To accurately detect and classify regions of replication across the genome, we present Repliscan. Repliscan robustly normalizes, automatically removes outlying and uninformative data points, and classifies Repli-seq signals into discrete combinations of replication signatures. The quality control steps and self-fitting methods make Repliscan generally applicable and more robust than previous methods that classify regions based on thresholds. Repliscan is simple and effective to use on organisms with different genome sizes. Even with analysis window sizes as small as 1 kilobase, reliable profiles can be generated with as little as 2.4x coverage.
ISSN:1471-2105
1471-2105
DOI:10.1186/s12859-017-1774-x