User: chrisclarkson100

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Posts by chrisclarkson100

<prev • 20 results • page 1 of 2 • next >
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Comment: C: circular genome visualisation: genomic.labels: Error in if (cr != chr) { : missi
... Hi Naveen, Sorry I'm so late to reply- I haven't been logged into this site for ages... I went through my notes on this project and I think that I just gave up on trying to fit 2 genomic density profiles and labels all in one plot... Instead I just went for one genomic density profile and labels on ...
written 3 months ago by chrisclarkson10030
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motifDb PFM vs JASPAR database PFM: conversion to PWM
... I apologise if some version of this question has already been asked in some way- I could not find any issues that were similar to my own. I have a choice between taking data from the datasource package 'MotifDb' and 'JASPAR2018': MotifDb has a much larger wealth of data: library (MotifDb) librar ...
motifdb jaspar pwm pfm written 9 months ago by chrisclarkson10030 • updated 7 months ago by Bioconductor Community ♦♦ 0
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(Closed) trying to reproduce heat map made via cBioportal using download data
... I need to make a statistical comparison using breast cancer data. I have made a heat map at the following link on the Bioportal: http://www.cbioportal.org/index.do?cancer_study_id=brca_tcga&Z_SCORE_THRESHOLD=2.0&RPPA_SCORE_THRESHOLD=2.0&data_priority=0&case_set_id=brca_tcga_mrna& ...
normalization heatmap cbioportal written 14 months ago by chrisclarkson10030
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circular genome visualisation: genomic.labels: Error in if (cr != chr) { : missing value where TRUE/FALSE needed
... I am finding your circlize package really useful. However, I am trying to label certain parts of the genome in my circular diagram with the function "genomic.labels" and getting the highlighted error below: library(circlize)   circos.initializeWithIdeogram(chromosome.index = paste0("chr", c(1:22,' ...
genomicfeatures rcircos written 18 months ago by chrisclarkson10030
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Error: unable to find an inherited method for function searchSeq for signature matrix
... I am trying to re-implement a script that I found on github (https://github.com/liz-is/ctcf-motif-imr90/blob/master/imr90_ctcf_motif_direction.R). This script finds the directionality of all CTCF sites in IMR90 cells. I would like to use this analysis for mm9 ESC cells. However I have run into a nu ...
tfbstools jaspar pwm written 23 months ago by chrisclarkson10030 • updated 23 months ago by Ge Tan20
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querying annotation hub for common TF, in common cell line returns no results....
... I am trying to query ENCODE for all the datasets it has on CTCF in the mm9 genome. I would have thought that this would be a fairly standard thing but it comes up with no results... hub=Annotationhub() ctcf_imr90 <- query(hub, c("ENCODE","CTCF", "Mus Musculus", "mm9"))   This produces no resu ...
annotate annotationhub written 23 months ago by chrisclarkson10030 • updated 23 months ago by shepherl ♦♦ 1.4k
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Comment: C: trying to annotate overlaps with external file information
... hi thank you- i should have looked through the intersectbed documentation and found out about the -wao option ...
written 2.3 years ago by chrisclarkson10030
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trying to annotate overlaps with external file information
... I have found the overlapping regions between the genomic regions I am interested in and genes with 'intersectBed'- external of R.  intersectBed -a regions_of_interest.bed -b genes.bed > overlap_genes.bed So now the file looks like this >head overlap_genes.bed chr1 180110925 1801135 ...
iranges granges written 2.3 years ago by chrisclarkson10030 • updated 2.3 years ago by Michael Lawrence11k
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R memory limit causing problems with genomicRanges operations...
... I have tried, using rtracklayer and Genomicranges to find the overlap between bed files that document different ChIP Seq data e.g. Nucleosome coverage, CTCF coverage etc. I want to then have a csv file that documents the overlapping regions and their occupancy levels e.g. "","seqnames","start","en ...
R bigmemory written 2.6 years ago by chrisclarkson10030 • updated 2.6 years ago by theobroma2210
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finding overlapping regions within 2 different bed files with different features
... Is it possible make a file in BED-like format in such a way that each row of data represents a region of the genome and then have different columns to specify the length, the GC content, the DNA methylation, the nucleosome occupancy, Nucleosome Repeat Length and as many features as one could gather, ...
annotation R written 2.8 years ago by chrisclarkson10030 • updated 2.8 years ago by Martin Morgan ♦♦ 23k

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