hmmCDR 0.1.7

Find CDR locations using bedmethyl file and CenSat annotations. (REQUIRES BEDTOOLS INSTALLED)

hmmCDR

hmmCDR is a set of python scripts to predict CDR regions of active alpha satellite arrays. It takes a bedMethyl from modkit and a set CenSat Annotations in order to make predictions.

Installation:

hmmCDR can be installed through conda. With bioconda and conda-forge channels enabled.

conda install jmmenend::hmmcdr -c bioconda -c conda-forge

hmmCDR can be run with docker.

docker run -v .:/data jmmenend/hmmcdr:0.1.4 # YOUR FLAGS #

hmmCDR can be install through pypi. Although this requires a separate installation of bedtools.

pip install hmmCDR

NOTE: If you chose it install with only pip you need to install bedtools as well.

Description:

This software is designed to find Centromere Dip Regions (CDRs), subCDRs, and their boundaries within the centromeric active alpha satellite (alpha-sat) array. CDRs are a uniquely hypo-methylated region within the typically hyper-methylated alpha-sat array. CDRs are tightly associated with the histone mark Centromere Protein A (CENP-A). This makes establishing accurate boundaries to CDRs and subCDRs essential to studying their relationship with CENPA. This method combines previous methods of identifying CDRs, through a sliding-window approach, with a Hidden Markov Model(HMM) that uses these sliding window estimates as a prior. The advantage to this two-fold approach is seen at the edges of the CDRs. A sliding window algorithm has a hard time drawing precise boundaries and identifying transitions in/out of the CDRs, whereas the HMM greatly improves identification of these regions.

* in this image the lighter blue represents a CDR transition.

This python package takes in a bed file of 5mC methylation in aggregate, preferably from modkit, and an Centromere-Satellite Annotation(CenSat) file. The aggregate methylation file is used to determine where the 5mC depleted regions are, and the CenSat Annotation is used to subset the methylation files to only the alpha-sat array. This improves both the speed and accuracy of the CDR identification, as outside this region the trend of hypermethylation is not as strong. This package also processes each chromosome separately and in parallel to further improve speed.

Inputs:

1. Modkit Pileup bedMethyl File:

column	name	description	type
1	chrom	name of chromosome/contig	str
2	start position	0-based start position	int
3	end position	0-based exclusive end position	int
4	modified base code	single letter code for modified base	str
5	score	Equal to Nvalid_cov.	int
6	strand	'+' for positive strand '-' for negative strand, '.' when strands are combined	str
7	start position	included for compatibility	int
8	end position	included for compatibility	int
9	color	included for compatibility, always 255,0,0	str
10	Nvalid_cov	Refer to modkit github	int
11	fraction modified	Nmod / Nvalid_cov	float
12	Nmod	Refer to modkit github	int
13	Ncanonical	Refer to modkit github	int
14	Nother_mod	Refer to modkit github	int
15	Ndelete	Refer to modkit github	int
16	Nfail	Refer to modkit github	int
17	Ndiff	Refer to modkit github	int
18	Nnocall	Refer to modkit github	int

2. CenSat Annotation bed

column	name	description	type
1	chrom	name of chromosome/contig	str
2	start position	0-based start position	int
3	end position	0-based exclusive end position	int
4	satellite type/name	type of satellite and for some specific name in parentheses	str
5	score	Not sure what if it is used for anytime.	int
6	strand	'+' for positive strand '-' for negative strand, '.' if uncertain	str
7	start position	included for compatibility	int
8	end position	included for compatibility	int
9	color	color of the annotation in browser	str

Usage:

usage: hmmCDR [-h] [-m MOD_CODE] [-s SAT_TYPE] [--bedgraph]
              [--min_valid_cov MIN_VALID_COV] [--window_size WINDOW_SIZE]
              [--prior_percent PRIOR_PERCENT]
              [--prior_transition_percent PRIOR_TRANSITION_PERCENT]
              [--raw_thresholds] [--n_iter N_ITER] [--no_transitions] [-w W]
              [-x X] [-y Y] [-z Z] [--merge_distance MERGE_DISTANCE]
              [--min_size MIN_SIZE] [--enrichment] [--main_color MAIN_COLOR]
              [--transition_color TRANSITION_COLOR] [--save_intermediates]
              [--output_label OUTPUT_LABEL]
              bedMethyl_path cenSat_path output_path

Process input files with optional parameters.

positional arguments:
  bedMethyl_path        Path to the bedMethyl file
  cenSat_path           Path to the CenSat BED file
  output_path           Output Path for the output files

optional arguments:
  -h, --help            show this help message and exit
  -m MOD_CODE, --mod_code MOD_CODE
                        Modification code to filter bedMethyl file (default:
                        "m")
  -s SAT_TYPE, --sat_type SAT_TYPE
                        Comma-separated list of satellite types/names to
                        filter CenSat bed file. (default: "H1L")
  --bedgraph            Flag indicating if the input is a bedgraph. (default:
                        False)
  --min_valid_cov MIN_VALID_COV
                        Minimum Valid Coverage to consider a methylation site.
                        (default: 10)
  --window_size WINDOW_SIZE
                        Window size to calculate prior regions. (default: 510)
  --prior_percent PRIOR_PERCENT
                        Percentile for finding priorCDR regions. (default: 10)
  --prior_transition_percent PRIOR_TRANSITION_PERCENT
                        Percentile for finding priorTransition regions.
                        (default: 20)
  --raw_thresholds      Use values for flags w,x,y,z as raw threshold cutoffs
                        for each emission category. (default: True)
  --n_iter N_ITER       Maximum number of iteration allowed for the HMM.
                        (default: 1)
  --no_transitions      Do not report transitions in final hmmCDR output file.
                        (default: False)
  -w W                  Threshold of non-zero methylation percentile to be
                        classified as very low (default: 0)
  -x X                  Threshold of non-zero methylation percentile to be
                        classified as low (default: 25)
  -y Y                  Threshold of non-zero methylation percentile to be
                        classified as medium (default: 50)
  -z Z                  Threshold of non-zero methylation percentile to be
                        classified as high (default: 75)
  --merge_distance MERGE_DISTANCE
                        Distance to merge adjacently labelled regions.
                        (default: 1021)
  --min_size MIN_SIZE   Minimum size for regions. (default: 3000)
  --enrichment          Enrichment flag. Pass in if you are looking for
                        methylation enriched regions. (default: False)
  --main_color MAIN_COLOR
                        Color to dictate main regions. (default: 50,50,255)
  --transition_color TRANSITION_COLOR
                        Color to dictate transition regions. (default:
                        100,150,200)
  --save_intermediates  Set to true if you would like to save
                        intermediates(filtered beds+window means). (default:
                        False)
  --output_label OUTPUT_LABEL
                        Label to use for name column of hmmCDR BED file. Needs
                        to match priorCDR label. (default: "CDR")

usage: hmmCDRprior [-h] [-m MOD_CODE] [-s SAT_TYPE] [--bedgraph]
                   [--min_valid_cov MIN_VALID_COV] [--window_size WINDOW_SIZE]
                   [--prior_percent PRIOR_PERCENT]
                   [--prior_transition_percent PRIOR_TRANSITION_PERCENT]
                   [--merge_distance MERGE_DISTANCE] [--min_size MIN_SIZE]
                   [--enrichment] [--output_label OUTPUT_LABEL]
                   [--save_intermediates]
                   bedMethyl_path cenSat_path output_path

Process bedMethyl and CenSat BED file to produce hmmCDR priors

positional arguments:
  bedMethyl_path        Path to the bedMethyl file
  cenSat_path           Path to the CenSat BED file
  output_path           Path to the output priorCDRs BED file

optional arguments:
  -h, --help            show this help message and exit
  -m MOD_CODE, --mod_code MOD_CODE
                        Modification code to filter bedMethyl file (default:
                        "m")
  -s SAT_TYPE, --sat_type SAT_TYPE
                        Comma-separated list of satellite types/names to
                        filter CenSat bed file. (default: "H1L")
  --bedgraph            Flag indicating if the input is a bedgraph. (default:
                        False)
  --min_valid_cov MIN_VALID_COV
                        Minimum valid coverage to consider a methylation
                        site(read from full modkit pileup files). (default:
                        10)
  --window_size WINDOW_SIZE
                        Window size to calculate prior regions. (default:
                        1020)
  --prior_percent PRIOR_PERCENT
                        Percentile for finding priorCDR regions. (default: 5)
  --prior_transition_percent PRIOR_TRANSITION_PERCENT
                        Percentile for finding priorTransition regions.
                        (default: 10)
  --merge_distance MERGE_DISTANCE
                        Percentile for finding priorTransition regions.
                        (default: 1021)
  --min_size MIN_SIZE   Minimum size for CDR regions. (default: 3000)
  --enrichment          Enrichment flag. Pass in if you are looking for
                        methylation enriched regions. (default: False)
  --output_label OUTPUT_LABEL
                        Label to use for name column of priorCDR BED file.
                        (default: "CDR")
  --save_intermediates  Set to true if you would like to save
                        intermediates(filtered beds+window means). (default:
                        False)

License

This project is licensed under the MIT License.