SeqArray-package {SeqArray} | R Documentation

## Data Management of Large-scale Whole-Genome Sequence Variant Calls

### Description

Data management of large-scale whole-genome sequencing variants.

### Details

As the cost of DNA sequencing rapidly decreases, whole-genome sequencing (WGS) is generating data at an unprecedented rate. Scientists are being challenged to manage data sets that are terabyte-sized, contain diverse types of data and complex data relationships. Data analyses of WGS requires a general file format for storing genetic variants including single nucleotide variations (SNVs), insertions and deletions (indels) and structural variants. The variant call format (VCF) is a generic and flexible format for storing DNA polymorphisms developed for the 1000 Genomes Project that is the standard WGS format in use today. VCF is a textual format usually stored in compressed files that supports rich annotations and relatively efficient data retrieval. However, VCF files are large and the computational burden associated with all data retrieval from text files can be significant for a large WGS study with thousands of samples.

To provide an efficient alternative to VCF for WGS data, we developed a new data format and accompanying Bioconductor package, “SeqArray”. Key features of SeqArray are efficient storage including multiple high compression options, data retrieval by variant or sample subsets, support for parallel access and computing, and C++ integration in the R programming environment. The SeqArray package provides R functions for efficient block-wise computations, and enables scientists to develop custom R scripts for exploratory data analysis.

Webpage: http://github.com/zhengxwen/SeqArray, http://www.bioconductor.org/packages/SeqArray/

### Author(s)

Xiuwen Zheng zhengxwen@gmail.com

### Examples

    # the file of VCF
    vcf.fn <- seqExampleFileName("vcf")
    vcf.fn
    # or vcf.fn <- "C:/YourFolder/Your_VCF_File.vcf"

    # parse the header
    seqVCF_Header(vcf.fn)

    # get sample id
    seqVCF_SampID(vcf.fn)

    # convert
    seqVCF2GDS(vcf.fn, "tmp.gds", storage.option="ZIP_RA")
    seqSummary("tmp.gds")

    # list the structure of GDS variables
    f <- seqOpen("tmp.gds")
    f

    seqClose(f)
    unlink("tmp.gds")

    ############################################################

    # the GDS file
    (gds.fn <- seqExampleFileName("gds"))

    # display
    (f <- seqOpen(gds.fn))

    # get 'sample.id
    (samp.id <- seqGetData(f, "sample.id"))
    # "NA06984" "NA06985" "NA06986" ...

    # get 'variant.id'
    head(variant.id <- seqGetData(f, "variant.id"))

    # get 'chromosome'
    table(seqGetData(f, "chromosome"))

    # get 'allele'
    head(seqGetData(f, "allele"))
    # "T,C" "G,A" "G,A" ...

    # set sample and variant filters
    seqSetFilter(f, sample.id=samp.id[c(2,4,6,8,10)])
    set.seed(100)
    seqSetFilter(f, variant.id=sample(variant.id, 10))

    # get genotypic data
    seqGetData(f, "genotype")

    # get annotation/info/DP
    seqGetData(f, "annotation/info/DP")

    # get annotation/info/AA, a variable-length dataset
    seqGetData(f, "annotation/info/AA")
    # $length              <- indicating the length of each variable-length data
    # [1] 1 1 1 1 1 1 ...
    # $data                <- the data according to $length
    # [1] "T" "C" "T" "C" "G" "C" ...

    # get annotation/format/DP, a variable-length dataset
    seqGetData(f, "annotation/format/DP")
    # $length              <- indicating the length of each variable-length data
    # [1] 1 1 1 1 1 1 ...
    # $data                <- the data according to $length
    #      variant
    # sample [,1] [,2] [,3] [,4] [,5] [,6] ...
    #  [1,]   25   25   22    3    4   17  ...

    # read multiple variables variant by variant
    seqApply(f, c(geno="genotype", phase="phase", qual="annotation/id"),
        FUN=function(x) print(x), as.is="none")

    # get the numbers of alleles per variant
    head(seqApply(f, "allele",
        FUN=function(x) length(unlist(strsplit(x,","))), as.is="integer"))
    # or
    head(seqGetData(f, "$num_allele"))

    ################################################################

    # remove the sample and variant filters
    seqResetFilter(f)

    # calculate the frequency of reference allele,
    #   a faster version could be obtained by C coding
    af <- seqApply(f, "genotype", FUN=function(x) mean(x==0L, na.rm=TRUE),
        as.is="double")
    length(af)
    summary(af)

    # close the GDS file
    seqClose(f)

[Package SeqArray version 1.27.15 Index]