ExomeCNV-package |
Exome Sequencing-Based CNV and LOH Detection. |
calculate.logR |
Calculate log ratio of depth of coverage between paired samples. |
chr.hash |
a data.frame of chromosome names to hash to numeric representation. |
chr.median |
Calculate log ratio of depth of coverage between paired samples. |
classify.eCNV |
Call CNV on each exon based on log ratio of read depth. |
classify.logR |
Call CNV on each exon based on log ratio of read depth. |
CNV.analyze |
A wrapper function of DNAcopy that prepare input and run CBS. |
cnv.points |
Plot CNV calls over log ratio. |
colors |
Constants used in the package. |
combine.baf |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
combine.CNV |
Combine results of DNAcopy and classify.eCNV into one table. |
combine.LOH |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
COVERAGE_HEADER |
Constants used in the package. |
do.DNAcopy |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
do.merge.cnv.intervals |
Combine results of DNAcopy and classify.eCNV into one table. |
do.merge.loh.intervals |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
do.plot.eCNV |
Plot CNV calls over log ratio. |
do.plot.loh |
Plot output of LOH calls. |
do.plot.one.eCNV |
Plot CNV calls over log ratio. |
do.plot.one.loh |
Plot output of LOH calls. |
ExomeCNV |
Exome Sequencing-Based CNV and LOH Detection. |
expand.loh |
Propagate LOH calls to all heterozygous positions within each LOH segment. |
find.max.of.2lists |
Pooling a compendium of "normal" exome samples. |
find.min.of.2lists |
Call LOH on each heterozygous position using specified test statistic. |
get.alpha |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.alpha.inv |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.AUC |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.end.position |
Call LOH on each heterozygous position using specified test statistic. |
get.power |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.power.inv |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.proper.cnv.positions |
A wrapper function of DNAcopy that prepare input and run CBS. |
get.r.cutoff |
Call CNV on each exon based on log ratio of read depth. |
get.sensitivity |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
get.specificity |
Calculate theoretical specificity, sensitivity, area under curve (AUC). |
good.percent |
Constants used in the package. |
guesstimate.contamination |
Estimate admixture/contamination rate in a sample. |
guesstimate.contarmination |
Estimate admixture/contamination rate in a sample. |
LOH.analyze |
Call LOH on each heterozygous position using specified test statistic. |
make.chunk |
Combine results of DNAcopy and classify.eCNV into one table. |
make.loh.chunk |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
make.loh.strata |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
MIL |
Constants used in the package. |
multi.CNV.analyze |
Use Circular Binary Segmentation to create segments and call CNV on each segment. |
multi.LOH.analyze |
Use Circular Binary Segmentation to create segments and call LOH on each segment based on BAF using specified method. |
my.cols |
Combine results of DNAcopy and classify.eCNV into one table. |
normalize.logR |
Calculate log ratio of depth of coverage between paired samples. |
one.sample.loh.test |
Call LOH on each heterozygous position using specified test statistic. |
phalfnorm |
Call LOH on each heterozygous position using specified test statistic. |
pool.coverage |
Pooling a compendium of "normal" exome samples. |
pool.coverage.from.files |
Pooling a compendium of "normal" exome samples. |
r.cutoffs |
Constants used in the package. |
RBIND_LIM |
Constants used in the package. |
read.all.coverage |
Read all coverage files by chromosome. |
read.coverage.gatk |
Read coverage file produced by The Genome Analysis Toolkit (GATK). |
read.coverage.gtf |
Read coverage file in GTF format as created by Howie Goodell. |
read.eCNV |
Read all .RData files produced by classify.eCNV(). |
read.gtf |
Read coverage file in GTF format as created by Howie Goodell. |
rho.list |
Constants used in the package. |
save.logR |
Save logR in files by chromosome. |
strip.chr.name |
A wrapper function of DNAcopy that prepare input and run CBS. |
test.num.copy |
Constants used in the package. |
two.sample.loh.CMH.test |
Call LOH on each heterozygous position using specified test statistic. |
two.sample.loh.deviation.test |
Call LOH on each heterozygous position using specified test statistic. |
two.sample.loh.test |
Call LOH on each heterozygous position using specified test statistic. |
window.sizes |
Constants used in the package. |
write.loh.output |
Generate an output file for LOH calls. |
write.output |
Generate output files from ExomeCNV outputs. |