normICE {HiTC} | R Documentation

## Iterative Correction of Hi-C data (ICE)

### Description

Iterative correction leverages the unique pairwise genome-wide structure of Hi-C data to decompose the data into a set of biases and a map of relative contact probabilities between any two genomic loci, achieving equal visibility across all genomic regions.

### Usage

    normICE(x, max_iter=50, eps=1e-4, sparse.filter=0.02)

### Arguments

`x` | object that inherits from class `HTCexp`
`max_iter` | maximum number of iteration
`eps` | the relative increment in the results before declaring convergence
`sparse.filter` | Define which pourcentage of bins with high sparsity should be force to zero

### Details

The normalization of Hi-C data is based on matrix balancing algorithm which consists of iteratively estimating the matrix bias using the l1 norm. The method implemented here is the Sinkhorn-Knopp algorithm as used in the Imakaev et al. paper. Note that the original method is applied on the genome-wide Hi-C map, but that the method could be applied on intra-chromosomal maps at high resolution.

### Value

Returns a `HTCexp` object with a corrected contact map.

### Author(s)

N. Servant, N. Varoqaux

### References

Imakaev M, Fudenberg G, McCord RP, Naumova N, Goloborodko A, Lajoie BR, Dekker J, Mirny LA. Iterative correction of Hi-C data reveals hallmarks of chromosome organization.Nat Methods. 2012 Oct;9(10):999-1003.

### See Also

`normLGF`

### Examples

    ## Not run:
    ##Lieberman data
    exDir <- system.file("extdata", package="HiTC")
    l <- sapply(list.files(exDir, pattern=paste("HIC_gm06690_"), full.names=TRUE),
                import.my5C)
    hiC <- HTClist(l)
    hiC <- hiC[isIntraChrom(hiC)]

    ## Run ICE
    hiC_iced <- HTClist(lapply(hiC, normICE))

    ## End(Not run)

[Package HiTC version 1.30.0 Index]