Description Usage Arguments Details Value Author(s) See Also Examples

This function estimates the library scaling factors that should be used for either a 'countData', or a matrix of counts and replicate information.

1 | ```
getLibsizes(cD, data, replicates, subset = NULL, estimationType = c("quantile", "total", "edgeR"), quantile = 0.75, ...)
``` |

`cD` |
A |

`data` |
A matrix of count values. Ignored if 'cD' is given. |

`replicates` |
A replicate structure for the data given in 'data'. Ignored if 'cD' is given. |

`subset` |
A numerical vector indicating the rows of the 'countData' object that should be used to estimate library scaling factors. |

`estimationType` |
One of 'quantile', 'total', or 'edgeR'. Partial matching is allowed. See Details. |

`quantile` |
A value between 0 and 1 indicating the level of trimming that should take place. See Details. |

`...` |
Additional parameters to be passed to the 'edgeR' calcNormFactors function. |

This function estimates the library scaling factors (surrogates for library size) in one of several ways, depending on the 'estimationType' argument. 'total' will give the library sizes by summing all counts in each sample. 'quantile' will give a library scaling factor by the method of Bullard et al (Bioinformatics 2010), summing all counts in each sample whose value below the qth quantile of non-zero counts for that sample. 'edgeR' uses the Trimmed Mean of M-vales (TMM) method of Robinson \& Oshlack (Genome Biology, 2010) via the 'edgeR' calcNormFactors function; other options are available through this function.

If a `countData`

object 'cD' is given, the library sizes
will be inferred from this. Alternatively, a matrix of count values
(columns are libraries) and a replicate structure (a vector defining
which samples belong to which replicate group) can be given.

If a `\link{countData}`

object is given, an identical object will
be returned with updated library sizes. If only the data and replicate
structure are given, a numerical vector of library sizes (scaling
factors) for each library in the data will be returned.

Thomas J. Hardcastle

1 2 3 4 5 6 | ```
data(simData)
replicates <- c(1,1,1,1,1,2,2,2,2,2)
groups <- list(c(1,1,1,1,1,1,1,1,1,1), c(1,1,1,1,1,2,2,2,2,2))
CD <- new("countData", data = simData, replicates = replicates, groups = groups)
libsizes(CD) <- getLibsizes(CD)
``` |

baySeq documentation built on Nov. 1, 2018, 5:05 a.m.

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