epiout 0.0.1

EpiOut: outlier detection for DNA accesibility data.

EpiOut

Install

Install epiout and its companion packages with:

pip install epiout

hic-straw is optional dependency to annotate chromatin interactions with EpiAnnot:

conda install -c bioconda hic-straw

or

conda install -c conda-forge curl
pip install hic-straw

and another optional dependency is onnxruntime to predict aberrant gene expression from aberrant chromatin accessibility:

pip install onnxruntime

Usage

Counting chromatin accessibility from ATAC-seq data with EpiCount:

epicount --bed {bed} --alignments {alignments.tsv} --output_prefix {output_prefix} --cores {threads}

where bed is a bed file of genomic regions to count accessibility, alignments.tsv is a tab-delimited file of ATAC-seq alignments, output_prefix is the prefix of output files, and threads is the number of threads to use. See epicount --help for more details.

alignments.tsv lists bam files of ATAC-seq alignments, one file per line, with the following columns:

path/a.bam
path/b.bam
path/c.bam

File names are used as sample names in the output files. Alternatively, you can use a tab-delimited file with the following columns to specify sample names:

path/a.bam	sample_a
path/b.bam	sample_b
path/c.bam	sample_c

EpiCount will generate three files: prefix.counts.parquet, prefix.raw_counts.parquet, prefix.bed. The parquet files containing the count matrix. The raw_counts file is not filtered for replication and counts file is filtered. bed file containing replicated the genomic regions across samples. The parquet file can be loaded with pandas and looking like:

df = pd.read_parquet('output_prefix.parquet')
df

EpiOut

To call outliers with EpiOut, run:

epiout --count_table {prefix.counts.parquet} --output_prefix {output_prefix} --cores {threads}

where count_table is the output of EpiCount, output_prefix is the prefix of output files, and threads is the number of threads to use. See epiout --help for more details. You can pass ordinary csv file of count matrix to --count_table argument where rows are genomic regions and columns are samples.

Output of EpiOut is prefix.h5ad file and prefix.results.csv. h5ad file contains statistics about outliers

from epiout import EpiOutResult

result = EpiOutResult.load('result.h5ad')

# outliers as dataframe
result.outlier

# log adjusted p-values as dataframe
result.log_padj

# results as dataframe alternatively read results.csv file
df_results = result.results()

# Visualize outliers or accessibile regions
result.qq_plot('chr1:100-200')
result.plot_counts('chr1:100-200')
result.plot_volcona('chr1:100-200')

See the documentation of EpiOutResult for more details.

EpiOut performs hyperparameter optimization to tune optimal bottleneck size of autoencoder. To specifiy the bottleneck size, use --bottleneck_size arguments.

EpiAnnot

epiannot_create --tissue {tissue or cell line name} --output_prefix {output_prefix}

where tissue is the name of tissue or cell line avaliable on ENCODE to fetch, output_prefix is the prefix of output files where config.yaml will be created and contains metadata and related files will be downloaded. See epiannot_create --help for more details:

Also you can check avaliable tissues or cell lines:

epiannot_list

To annotate accesible regions and chromatin interactions with EpiAnnot, run:

epiannot --bed {bed} --gtf {gtf} --counts {prefix.h5ad} --chrom_sizes {chrom_sizes} --output_prefix {output_prefix}

where bed is a bed file of genomic regions to annotate, gtf is a gtf file of gene annotations, counts is the output of EpiOut in h5ad file format or counts obtained with EpiCount, chrom_sizes is a file of chromosome sizes can be generated with pyfaidx from fasta file, and output_prefix is the prefix of output files. See epiannot --help for more details.

Output contains prefix.annotation.csv annotation of genomic regions based on histone marks provided in the config file, prefix.gtf.csv annotation on regions based on the proximity to genes, prefix.interaction.csv annotation of chromatin interactions between regions and prefix.genes.csv indicating that poteintial effected by the aberrant chromatin accessibility.

You can create annotation with your custom config file:

config.yaml

H3K27ac:
- ENCFF817IVB.bed.gz
- ENCFF916FML.bed.gz

H3K4me1:
- ENCFF456GWH.bed.gz

H3K4me3:
- ENCFF867WVM.bed.gz

your_custom_mark:
- a.bed

hic:
- ENCFF311CLH.hic
- ENCFF787ZVA.hic

They keys in the config file are the names of histone marks and the values are the list of bed files of histone marks. The config file can also contain a list of hic files to annotate chromatin interactions. Hic data is optional. The config file can be created with epiannot_create command or you can use your config file. To call promoter, active and poised enhancers please make sure that you name your histone marks as H3K4me3, H3K27ac, and H3K4me1 respectively. An other histone mark or bed files can be used annotate regions. Output prefix.annotation.csv will have a column for each key in the config file and will incidate if accesible region overlaps with the annotation source.