View source: R/platypusFilter.R
platypusFilter | R Documentation |
This function executes platypusFilter filtering the single_variants.vcf generated by platypys function.
platypusFilter(
group = c("sudo", "docker"),
data.folder = getwd(),
scratch.folder,
GQ,
minSampGQ,
NR,
minSampNR,
NV,
minSampNV,
normal_samples,
GT_normal,
minSampGT_normal,
tumoral_samples,
GT_tumoral,
minSampGT_tumoral,
stringent_filter,
annotation
)
group |
a character string. Two options: sudo or docker, depending to which group the user belongs |
data.folder |
a character string indicating the folder where bams and vcf files are located and where output will be written |
scratch.folder |
a character string indicating the path of the scratch folder |
GQ |
min GQ value to consider (extreme included) |
minSampGQ |
min number of samples with GQ value (extreme included), usually we start with 85% of the samples |
NR |
min NR value to consider (extreme included), the number of reads covering the SNV region |
minSampNR |
min number of samples with NR value (extreme included), usually we start with 85% of the samples |
NV |
min NV value to consider (extreme included), the n of reads with the SNV |
minSampNV |
min number of samples with NV value (extreme included) |
normal_samples |
string with names (group names of bam files) of normal samples separated by hash, write NULL if you do not want to use GT filter in normal samples |
GT_normal |
GT value in normal samples to consider, type "NO" if you do not want to use this filter, else e.g. you might use 0/0 |
minSampGT_normal |
min number of normal samples with GT value |
tumoral_samples |
string with names (group names of bam files) of tumoral samples separated by &, write NULL if you do not want to use GT filter in normal samples |
GT_tumoral |
GT value in tumoral samples to consider, type "NO" if you do not want to use this filter. Type e.g. 0/0 if you do not want to consider this genotype. |
minSampGT_tumoral |
min number of tumoral samples in which the GT value is NOT present |
stringent_filter |
To enable the filter (it keeps only the variants with "PASS" value or the variants that have only the "alleleBias" value) use 1 or 0 to disable it |
annotation |
hg19 and mm10 are actually available for the annotation of the detected SNVs |
Riccardo Panero, riccardo.panero[at]gmail[dot]com, Bioinformatics and Genomics unit, University of Torino Italy
## Not run:
#filtering platypus results
platypusFilter(group="docker", data.folder="/archive/home/rcaloger/data/platypus_tests/mm10ENSEMBL",
scratch.folder="/scratch/users/rcaloger/",
GQ=10, minSampGQ=2, NR=10, minSampNR=2, NV=3,
minSampNV=1, normal_samples="MAMBO43", GT_normal="0/0",
minSampGT_normal=1, tumoral_samples="MAMBO43TRT#MAMBO43TRNT", GT_tumoral="0/0",
minSampGT_tumoral=1, stringent_filter=0, annotation="mm10")
## End(Not run)
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