crr-labels 1.0.4

FANTOM

To retrieve the FANTOM promoters and enhancers you can proceed as follows:

from crr_labels import fantom

enhancers, promoters = fantom(
    cell_lines=["HelaS3", "GM12878"], # list of cell lines to be considered.
    window_size=200, # window size to use for the various regions.
    genome = "hg19", # considered genome version. Currently supported only "hg19".
    center_enhancers = "peak", # how to center the enhancer window, either around "peak" or the "center" of the region.
    enhancers_threshold = 0, # activation threshold for the enhancers.
    promoters_threshold = 5, # activation threshold for the promoters.
    drop_always_inactive_rows = True, # whetever to drop the rows where no activation is detected for every rows.
    binarize: bool= True, # Whetever to return the data binary-encoded, zero for inactive, one for active.
    nrows:int=None # the number of rows to read, usefull when testing pipelines for creating smaller datasets.
)

The library will download and parse the fantom project raw data and return two dataframes for the required cell lines. Consider reading the method docstring for more id-depth informations about the method.

The main steps are the following:

• The raw files are retrieved from the fantom dataset from the link specified in the fantom_data.json file

• The window for the enhancers and promoters are expanded or compressed to the given window size. In particular:

  • The enhancers window can either be centered on the region center with the “center” mode or around the “peak” with the “peak” mode.

  • The promoters window is upstream in the positive strand from the end of the promoter and downstream on the negative strand from the start of the promoter.

• When multiple experiments are present for a cell line, for instance for “HelaS3”, an average of the activation peaks is executed.

• Optionally (and by default) the rows that are always inactive for the chosen cell lines are dropped. You can specify this behaviour using the parameter “drop_always_inactive_rows”.

Roadmap

To retrieve the Roadmap promoters and enhancers you can proceed as follows:

from crr_labels import roadmap

enhancers, promoters = roadmap(
    cell_lines=["HelaS3", "GM12878"], # List of cell lines to be considered.
    window_size=200, # Window size to use for the various regions.
    genome = "hg19", # Considered genome version. Currently supported only "hg19".
    states: int = 18, # Number of the states of the model to consider. Currently supported only "15" and "18".
    enhancers_labels: List[str] = ("7_Enh", "9_EnhA1", "10_EnhA2"), # Labels to encode as active enhancers.
    promoters_labels: List[str] = ("1_TssA",), # Labels to enode as active promoters.
    nrows:int=None # the number of rows to read, usefull when testing pipelines for creating smaller datasets.
)

Consider reading the method docstring for more id-depth informations about the method.

FANTOM

The following datasets contain data for the cell lines GM12878, HelaS3, HepG2, K562, A549, H1, H9, JURKAT, MCF7, HEK293, Caco2, HL60 and PC3.

Roadmap

The following datasets contain data for the cell lines GM12878, HelaS3, HepG2, K562, A549, H1, H9, DND41, HUES48, HUES6, HUES64 and IMR90.