Description Usage Arguments Details Value Examples
This function reads data in .SNP (quality_variant) format, as distributed by the 1001 Genomes project (Arabidopsis).
1 2 3 4 5 |
folder |
the basepath of the variant_calls |
outgroup |
vector of outgroup sequences |
populations |
list of populations |
gffpath |
the corresponding GFF file |
CHR |
which chromosome ?, default: all chromosomes |
ref.chr |
reference chromosome (to classify synonymous/non-synonymous positions) |
snp.window.size |
scan SNP chunks |
parallized |
multicore computation |
ffpackagebool |
use the ff-package to save memory space. (slower) |
include.unknown |
include positions with unknown nucleotides |
The ff-package we use to store the SNP information limits the data size to
individuals * (number of SNPs) <= .Machine$integer.max
The text files containing the SNP information of each individual have to be stored in one folder.
The slots transitions
, biallelic.sites
, and biallelic.substitutions
of the class
"regions.data"
will be filled.
At this time, if a GFF/GTF is used the data should be organized in a way that
the "CHR" is a numerical value. The prefix "Chr" or "chr" is also supported.
The function creates an object of class "GENOME"
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Following Slots will be filled in the "GENOME"
object
———————————————————
Slot | Description | |
1. | n.sites | total number of sites |
2. | n.biallelic.sites | number of biallelic sites |
3. | region.data | some detailed information about the data read |
4. | region.names | names of regions |
1 2 3 4 5 6 7 8 | # GENOME.class <- readSNP("...\SNPData")
# GENOME.class <- readSNP("...\SNPData", CHR=1)
# GENOME.class <- readSNP("...\SNPData", CHR=1, gffpath="Gff_file.gff")
# GENOME.class
# GENOME.class <- neutrality.stats(GENOME.class,FAST=TRUE)
# show the result:
# get.sum.data(GENOME.class)
# GENOME.class@region.data
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