parallel_sample_ichor_capture | R Documentation |
IchorCNA implementation for Capture Panel Data
parallel_sample_ichor_capture(
cnrs = "",
patient_id = "",
normal = 0.5,
ploidy = 2,
maxCN = 7,
includeHOMD = FALSE,
scStates = c(1, 3),
txnE = 0.9999999,
txnStrength = 1e+07,
output_dir = ".",
min_cov = -15,
lambda = NULL,
coverage = NULL,
minSegmentBins = 50,
minTumFracToCorrect = 0.01,
chrs = c(1:22, "X"),
chrTrain = seq(1:22),
gender = "male",
maxFracCNASubclone = 0.7,
maxFracGenomeSubclone = 0.5,
lambdaScaleHyperParam = 3,
altFracThreshold = 0.05,
estimateNormal = TRUE,
estimatePloidy = TRUE,
estimateScPrevalence = TRUE,
plotYLim = c(-2, 2),
plotFileType = "pdf",
verbose = FALSE,
batch_config = build_default_preprocess_config(),
threads = 4,
ram = 4,
mode = "local",
executor_id = make_unique_id("parSamplehybridIchorCNA"),
task_name = "parSamplehybridIchorCNA",
time = "48:0:0",
update_time = 60,
wait = FALSE,
hold = NULL
)
cnrs |
REQUIRED Path to tumour CNR file. |
normal |
OPTIONAL Path to normal samples. Default c(0.5,0.6,0.7,0.8,0.9) |
ploidy |
OPTIONAL Initial tumour ploidy; can be more than one value if additional ploidy initializations are desired. Default: 2 |
maxCN |
OPTIONAL Total clonal states. Default 7. |
includeHOMD |
OPTIONAL If FALSE, then exclude HOMD state. Useful when using large bins (e.g. 1Mb). Default FALSE. |
scStates |
OPTIONAL Subclonal states to consider. Default NULL |
txnE |
OPTIONAL Self-transition probability. Increase to decrease number of segments. Default: 0.9999999 |
txnStrength |
OPTIONAL Transition pseudo-counts. Exponent should be the same as the number of decimal places of –txnE. Default: 1e+07 |
output_dir |
OPTIONAL Path to the output directory. |
lambda |
OPTIONAL Initial Student's t precision; must contain 4 values (e.g. c(1500,1500,1500,1500)); if not provided then will automatically use based on variance of data |
minSegmentBins |
OPTIONAL Minimum number of bins for largest segment threshold required to estimate tumor fraction; if below this threshold, then will be assigned zero tumor fraction |
maxFracCNASubclone |
OPTIONAL Exclude solutions with fraction of subclonal events greater than this value. Default 0.7 |
maxFracGenomeSubclone |
OPTIONAL Exclude solutions with subclonal genome fraction greater than this value. Default 0.5 |
lambdaScaleHyperParam |
OPTIONAL Hyperparameter (scale) for Gamma prior on Student's-t precision. Default 3 |
altFracThreshold |
OPTIONAL Minimum proportion of bins altered required to estimate tumor fraction; if below this threshold, then will be assigned zero tumor fraction. Default: 0.05 |
estimateNormal |
OPTIONAL Estimate normal. Default TRUE. |
estimatePloidy |
OPTIONAL Estimate tumour ploidy. Default TRUE. |
estimateScPrevalence |
OPTIONAL Estimate subclonal prevalence. Default TRUE. |
plotYLim |
OPTIONAL ylim to use for chromosome plots. Default: c(-2,2) |
plotFileType |
OPTIONAL File format for output plots. Default pdf |
verbose |
OPTIONAL Enables progress messages. Default False. |
threads |
OPTIONAL Number of threads to split the work. Default 4 |
ram |
OPTIONAL RAM memory to asing to each thread. Default 4 |
mode |
REQUIRED Where to parallelize. Default local. Options "local","batch" |
executor_id |
Task EXECUTOR ID. Default "recalCovariates" |
task_name |
Task name. Default "recalCovariates" |
time |
OPTIONAL If batch mode. Max run time per job. Default "48:0:0" |
update_time |
OPTIONAL If batch mode. Job update time in seconds. Default 60. |
wait |
OPTIONAL If batch mode wait for batch to finish. Default FALSE |
hold |
OPTIONAL HOld job until job is finished. Job ID. |
output_name |
OPTIONAL Name for the output. If not given the name of the first tumour sample of the samples will be used. |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.