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As a bioinformatician, I would like to calculate the average DNA methylation across a range of region types across the genome in a single cell, in order to create later overview plots of a given data set.
Regions should be able to be fed in via bed files; the best way to pass in a list of bed files in CWL should be investigated. Example region types: all gene bodies, all introns, all exons, all CpG islands, all promoters, all repetitive elements, known enhancer sites, etc.
One other thought: many of these may be contained within LOLA, and this is essentially the same task as #28 , in which case code could be replicated. It may be necessary to be able to take in a combination of LOLA data and external BED files, and we should think about how to combine these.
Actually, merging this with #28: As a bioinformatician, I would like to calculate the average DNA methylation across a series of known DNA-associated protein binding footprint regions based on ChIP-seq experiments, using data from the LOLA package (ie the ENCODE and Codex data sets), in order to later find binding footprints associated with DMRs/conditions.
ie: make one CWL tool that takes in BED files, and another that specifies LOLA data sets
The text was updated successfully, but these errors were encountered:
Description
As a bioinformatician, I would like to calculate the average DNA methylation across a range of region types across the genome in a single cell, in order to create later overview plots of a given data set.
Estimate
5
Priority
MUST
Notes
@oneillkza has code which can be adapted for this
Regions should be able to be fed in via bed files; the best way to pass in a list of bed files in CWL should be investigated. Example region types: all gene bodies, all introns, all exons, all CpG islands, all promoters, all repetitive elements, known enhancer sites, etc.
One other thought: many of these may be contained within LOLA, and this is essentially the same task as #28 , in which case code could be replicated. It may be necessary to be able to take in a combination of LOLA data and external BED files, and we should think about how to combine these.
Actually, merging this with #28: As a bioinformatician, I would like to calculate the average DNA methylation across a series of known DNA-associated protein binding footprint regions based on ChIP-seq experiments, using data from the LOLA package (ie the ENCODE and Codex data sets), in order to later find binding footprints associated with DMRs/conditions.
ie: make one CWL tool that takes in BED files, and another that specifies LOLA data sets
The text was updated successfully, but these errors were encountered: