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Description |
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~~~~~~~~~~~ |
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Util to convert Arabicto Roman
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Utility to convert Arabic numbers to Roman numbers
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Usage |
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~~~~~ |
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Description |
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~~~~~~~~~~~ |
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Util to convert Roman to Arabic
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Utility to convert Roman numbers into Arabic numbers
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Usage |
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~~~~~ |
... | ... | |
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Description |
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~~~~~~~~~~~ |
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This function aggregates nucleosome for replicated samples. It uses
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This function aggregates nucleosomes from replicated samples. It uses
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TemplateFilter ouput of each sample as replicate. Each sample owns a set |
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of nucleosomes computed using TemplateFilter and ordered by the position |
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of their center. Adajacent nucleosomes are compared two by two. |
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Comparison is based on a log likelihood ratio score. The issue of |
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comparison is adjacents nucleosomes merge or separation. Finally the |
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function returns a list of clusters and all computed *llr\_scores*. Each |
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cluster ows an attribute *wp* for "well positionned". This attribute is |
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set as *TRUE* if the cluster is composed of exactly one nucleosomes of |
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each sample. |
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of their center (dyad). A chain of nucleosomes is builts across all |
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replicates. Adjacent nucleosomes of the chain are compared two by two. |
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Comparison is based on a log likelihood ratio (LLR1). depending on the |
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LLR1 value nucleosomes are merged (low LLR) or separated (high LLR). |
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Finally the function returns a list of clusters and all computed |
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llr\_scores. Each cluster ows an attribute wp for “well positioned”. |
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This attribute is set to TRUE if the cluster is composed of exactly one |
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nucleosome of each sample. |
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Usage |
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~~~~~ |
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``llr_thres`` |
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Log likelihood ration threshold.
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Log likelihood ratio threshold to decide between merging and separating
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``coord_max`` |
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Description |
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~~~~~~~~~~~ |
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This function aligns nucs between two strains for a given genome region. |
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This function aligns nucleosomes between two strains for a given genome |
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region. |
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Usage |
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~~~~~ |
... | ... | |
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``wp_nucs_strain_ref1`` |
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List of aggregates nucleosome for strain 1. If it's null this list will
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List of aggregates nucleosome for strain 1. If it's NULL this list will
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be computed. |
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``wp_nucs_strain_ref2`` |
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List of aggregates nucleosome for strain 2. If it's null this list will
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List of aggregates nucleosome for strain 2. If it's NULL this list will
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be computed. |
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``corr_thres`` |
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``llr_thres`` |
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LOD cut off.
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Log likelihood ratio threshold to decide between merging and separating
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``config`` |
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} |
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print(align_inter_strain_nucs(replicates)) |
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R: Launch deseq methods.
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R: Launch DESeq methods.
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Launch deseq methods.
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Launch DESeq methods.
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--------------------- |
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Description |
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~~~~~~~~~~~ |
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This function is based on deseq example. It mormalizes data, fit data to |
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GLM model with and without interaction term and compare the two |
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l;=models. |
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This function is based on DESeq example. It normalizes data, fit data to |
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GLM model with and without interaction term and compares the two models. |
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Usage |
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~~~~~ |
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``snep_design`` |
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The design to considere.
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The design to consider. |
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``reads`` |
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The data to considere.
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The data to consider. |
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Author(s) |
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~~~~~~~~~ |
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Description |
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~~~~~~~~~~~ |
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This function loads in memory data corresponding to the given |
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This function loads in memory the data corresponding to the given
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experiments. |
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Usage |
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``expe`` |
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a list of vector corresponding to vector of replicates.
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a list of vectors corresponding to replicates.
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``roi`` |
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# library(nucleominer) |
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# |
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# # Read config file |
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# json_conf_file = "nucleo_miner_config.json"
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# json_conf_file = "nucleominer_config.json" |
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# config = fromJSON(paste(readLines(json_conf_file), collapse="")) |
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# # Read sample file |
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# all_samples = get_content(config$CSV_SAMPLE_FILE, "cvs", sep=";", head=TRUE, stringsAsFactors=FALSE) |
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Description |
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~~~~~~~~~~~ |
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This fonction allow to acces to a specific part of the c2c file.
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This fonction allows to access to a specific part of the c2c file.
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Usage |
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~~~~~ |
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``chr`` |
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if defined, the c2c will filtered according to the chromosome value |
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if defined, the c2c will be filtered according to the chromosome value
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``lower_bound`` |
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if defined, the c2c will filtered for part of the genome upper than |
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if defined, the c2c will be filtered for part of the genome upper than
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lower\_bound |
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``upper_bound`` |
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if defined, the c2c will filtered for part of the genome lower than |
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if defined, the c2c will be filtered for part of the genome lower than
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upper\_bound |
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``config`` |
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Florent Chuffart |
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R: Build the design for deseq
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R: Build the design for DESeq
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Build the design for deseq
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Build the design for DESeq
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-------------------------- |
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Description |
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:: |
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get_sneps(marker, combi, form, all_samples, config = NULL) |
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get_sneps(marker, combi, form, all_samples, FDR = 1e-04, config = NULL)
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Arguments |
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~~~~~~~~~ |
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Global list of samples. |
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``FDR`` |
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``config`` |
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GLOBAL config variable |
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:: |
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# LOD score for 2 set of values
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# LLR score for 2 set of values
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mean1=5; sd1=2; card2 = 250 |
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mean2=6; sd2=3; card1 = 200 |
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x1 = rnorm(card1, mean1, sd1) |
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Description |
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~~~~~~~~~~~ |
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This fuxntion use the deseq nomalization feature to compare
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This fuxntion use the DESeq nomalization feature to compare
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qualitatively the distribution. |
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Usage |
... | ... | |
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Description |
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~~~~~~~~~~~ |
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This function is an eloborated call to translate\_cur.
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This function is an elaborated call to translate\_cur.
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Usage |
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~~~~~ |
... | ... | |
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Florent Chuffart |
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R: Aggregate regions that intersect themnselves.
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R: Aggregate regions that intersect themselves. |
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Aggregate regions that intersect themnselves.
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---------------------------------------------
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Aggregate regions that intersect themselves. |
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-------------------------------------------- |
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Description |
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~~~~~~~~~~~ |
Formats disponibles : Unified diff