In [1]:
import os
import sys
sys.path.append(os.path.abspath("/users/amtseng/tfmodisco/src/"))
from tfmodisco.run_tfmodisco import import_shap_scores, import_tfmodisco_results
from motif.read_motifs import pfm_info_content, pfm_to_pwm, trim_motif_by_ic
from motif.match_motifs import match_motifs_to_database
from util import figure_to_vdom_image
import plot.viz_sequence as viz_sequence
import numpy as np
import h5py
import matplotlib.pyplot as plt
import vdom.helpers as vdomh
from IPython.display import display

Define constants and paths

In [2]:
# Define parameters/fetch arguments
tf_name = os.environ["TFM_TF_NAME"]
shap_scores_path = os.environ["TFM_SHAP_PATH"]
tfm_results_path = os.environ["TFM_TFM_PATH"]
hyp_score_key = os.environ["TFM_HYP_SCORE_KEY"]
if "TFM_MOTIF_CACHE" in os.environ:
    tfm_motifs_cache_dir = os.environ["TFM_MOTIF_CACHE"]
else:
    tfm_motifs_cache_dir = None

print("TF name: %s" % tf_name)
print("DeepSHAP scores path: %s" % shap_scores_path)
print("TF-MoDISco results path: %s" % tfm_results_path)
print("Importance score key: %s" % hyp_score_key)
print("Saved TF-MoDISco-derived motifs cache: %s" % tfm_motifs_cache_dir)
TF name: E2F6
DeepSHAP scores path: /users/amtseng/tfmodisco/results/importance_scores/multitask_profile/E2F6_multitask_profile_fold2/E2F6_multitask_profile_fold2_imp_scores.h5
TF-MoDISco results path: /users/amtseng/tfmodisco/results/tfmodisco/multitask_profile/E2F6_multitask_profile_fold2/E2F6_multitask_profile_fold2_count_tfm.h5
Importance score key: count_hyp_scores
Saved TF-MoDISco-derived motifs cache: /users/amtseng/tfmodisco/results/reports/tfmodisco_results//cache/multitask_profile/E2F6_multitask_profile_fold2/E2F6_multitask_profile_fold2_count
In [3]:
# Define paths and constants
input_length = 2114
shap_score_center_size = 400
In [4]:
if tfm_motifs_cache_dir:
    os.makedirs(tfm_motifs_cache_dir, exist_ok=True)

Import SHAP scores and TF-MoDISco results

In [5]:
# Import SHAP coordinates and one-hot sequences
hyp_scores, _, one_hot_seqs, shap_coords = import_shap_scores(shap_scores_path, hyp_score_key, center_cut_size=shap_score_center_size)
# This cuts the sequences/scores off just as how TF-MoDISco saw them, but the coordinates are uncut
Importing SHAP scores: 100%|██████████| 52/52 [00:36<00:00,  1.43it/s]
In [6]:
# Import the TF-MoDISco results object
tfm_obj = import_tfmodisco_results(tfm_results_path, hyp_scores, one_hot_seqs, shap_score_center_size)

Plot some SHAP score tracks

Plot the central region of some randomly selected actual importance scores

In [7]:
plot_slice = slice(int(shap_score_center_size / 4), int(3 * shap_score_center_size / 4))
for index in np.random.choice(hyp_scores.shape[0], size=5, replace=False):
    viz_sequence.plot_weights((hyp_scores[index] * one_hot_seqs[index])[plot_slice], subticks_frequency=100)

Plot TF-MoDISco results

Plot all motifs by metacluster

In [8]:
motif_pfms, motif_hcwms, motif_cwms = [], [], []  # Save the trimmed PFMs, hCWMs, and CWMs
motif_pfms_short = []  # PFMs that are even more trimmed (for TOMTOM)
num_seqlets = []  # Number of seqlets for each motif
motif_seqlets = []  # Save seqlets of each motif
metaclusters = tfm_obj.metacluster_idx_to_submetacluster_results
num_metaclusters = len(metaclusters.keys())
if tfm_motifs_cache_dir:
    motif_hdf5 = h5py.File(os.path.join(tfm_motifs_cache_dir, "all_motifs.h5"), "w")
for metacluster_i, metacluster_key in enumerate(metaclusters.keys()):
    metacluster = metaclusters[metacluster_key]
    display(vdomh.h3("Metacluster %d/%d" % (metacluster_i + 1, num_metaclusters)))
    patterns = metacluster.seqlets_to_patterns_result.patterns
    if not patterns:
        break
    motif_pfms.append([])
    motif_hcwms.append([])
    motif_cwms.append([])
    motif_pfms_short.append([])
    num_seqlets.append([])
    motif_seqlets.append([])
    num_patterns = len(patterns)
    for pattern_i, pattern in enumerate(patterns):
        seqlets = pattern.seqlets
        display(vdomh.h4("Pattern %d/%d" % (pattern_i + 1, num_patterns)))
        display(vdomh.p("%d seqlets" % len(seqlets)))
        
        pfm = pattern["sequence"].fwd
        hcwm = pattern["task0_hypothetical_contribs"].fwd
        cwm = pattern["task0_contrib_scores"].fwd
        
        pfm_fig = viz_sequence.plot_weights(pfm, subticks_frequency=10, return_fig=True)
        hcwm_fig = viz_sequence.plot_weights(hcwm, subticks_frequency=10, return_fig=True)
        cwm_fig = viz_sequence.plot_weights(cwm, subticks_frequency=10, return_fig=True)
        pfm_fig.tight_layout()
        hcwm_fig.tight_layout()
        cwm_fig.tight_layout()
        
        motif_table = vdomh.table(
            vdomh.tr(
                vdomh.td("Sequence (PFM)"),
                vdomh.td(figure_to_vdom_image(pfm_fig))
            ),
            vdomh.tr(
                vdomh.td("Hypothetical contributions (hCWM)"),
                vdomh.td(figure_to_vdom_image(hcwm_fig))
            ),
            vdomh.tr(
                vdomh.td("Actual contributions (CWM)"),
                vdomh.td(figure_to_vdom_image(cwm_fig))
            )
        )
        display(motif_table)
        plt.close("all")  # Remove all standing figures
        
        # Trim motif based on information content
        short_trimmed_pfm = trim_motif_by_ic(pfm, pfm)
        motif_pfms_short[-1].append(short_trimmed_pfm)
        
        # Expand trimming to +/- 4bp on either side
        trimmed_pfm = trim_motif_by_ic(pfm, pfm, pad=4)
        trimmed_hcwm = trim_motif_by_ic(pfm, hcwm, pad=4)
        trimmed_cwm = trim_motif_by_ic(pfm, cwm, pad=4)
        
        motif_pfms[-1].append(trimmed_pfm)
        motif_hcwms[-1].append(trimmed_hcwm)
        motif_cwms[-1].append(trimmed_cwm)
        
        num_seqlets[-1].append(len(seqlets))
        
        if tfm_motifs_cache_dir:
            # Save results and figures
            motif_id = "%d_%d" % (metacluster_i, pattern_i)
            pfm_fig.savefig(os.path.join(tfm_motifs_cache_dir, motif_id + "_pfm_full.png"))
            hcwm_fig.savefig(os.path.join(tfm_motifs_cache_dir, motif_id + "_hcwm_full.png"))
            cwm_fig.savefig(os.path.join(tfm_motifs_cache_dir, motif_id + "_cwm_full.png"))
            motif_dset = motif_hdf5.create_group(motif_id)
            motif_dset.create_dataset("pfm_full", data=pfm, compression="gzip")
            motif_dset.create_dataset("hcwm_full", data=hcwm, compression="gzip")
            motif_dset.create_dataset("cwm_full", data=cwm, compression="gzip")
            motif_dset.create_dataset("pfm_trimmed", data=trimmed_pfm, compression="gzip")
            motif_dset.create_dataset("hcwm_trimmed", data=trimmed_hcwm, compression="gzip")
            motif_dset.create_dataset("cwm_trimmed", data=trimmed_cwm, compression="gzip")
            motif_dset.create_dataset("pfm_short_trimmed", data=short_trimmed_pfm, compression="gzip")

Metacluster 1/1

Pattern 1/6

5628 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Pattern 2/6

4615 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Pattern 3/6

2547 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Pattern 4/6

963 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Pattern 5/6

525 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Pattern 6/6

224 seqlets

Sequence (PFM)
Hypothetical contributions (hCWM)
Actual contributions (CWM)

Summary of motifs

Motifs are trimmed based on information content, and presented in descending order by number of supporting seqlets. The motifs are separated by metacluster. The motifs are presented as hCWMs. The forward orientation is defined as the orientation that is richer in purines.

In [9]:
colgroup = vdomh.colgroup(
    vdomh.col(style={"width": "5%"}),
    vdomh.col(style={"width": "5%"}),
    vdomh.col(style={"width": "45%"}),
    vdomh.col(style={"width": "45%"})
)
header = vdomh.thead(
    vdomh.tr(
        vdomh.th("#", style={"text-align": "center"}),
        vdomh.th("Seqlets", style={"text-align": "center"}),
        vdomh.th("Forward", style={"text-align": "center"}),
        vdomh.th("Reverse", style={"text-align": "center"})
    )
)

for i in range(len(motif_hcwms)):
    display(vdomh.h3("Metacluster %d/%d" % (i + 1, num_metaclusters)))
    body = []
    for j in range(len(motif_hcwms[i])):
        motif = motif_hcwms[i][j]
        if np.sum(motif[:, [0, 2]]) > 0.5 * np.sum(motif):
            # Forward is purine-rich, reverse-complement is pyrimidine-rich
            f, rc = motif, np.flip(motif, axis=(0, 1))
        else:
            f, rc = np.flip(motif, axis=(0, 1)), motif
            
        f_fig = viz_sequence.plot_weights(f, figsize=(20, 4), return_fig=True)
        f_fig.tight_layout()
        rc_fig = viz_sequence.plot_weights(rc, figsize=(20, 4), return_fig=True)
        rc_fig.tight_layout()
        
        if tfm_motifs_cache_dir:
            # Save results and figures
            motif_id = "%d_%d" % (i, j)
            f_fig.savefig(os.path.join(tfm_motifs_cache_dir, motif_id + "_hcwm_trimmed_fwd.png"))
            rc_fig.savefig(os.path.join(tfm_motifs_cache_dir, motif_id + "_hcwm_trimmed_rev.png"))

        body.append(
            vdomh.tr(
                vdomh.td(str(j + 1)),
                vdomh.td(str(num_seqlets[i][j])),
                vdomh.td(figure_to_vdom_image(f_fig)),
                vdomh.td(figure_to_vdom_image(rc_fig))
            )
        )
    display(vdomh.table(colgroup, header, vdomh.tbody(*body)))
    plt.close("all")

Metacluster 1/1

#SeqletsForwardReverse
15628
24615
32547
4963
5525
6224

Top TOMTOM matches for each motif

Here, the TF-MoDISco motifs are plotted as hCWMs, but the TOMTOM matches are shown as PWMs.

In [10]:
num_matches_to_keep = 10
num_matches_to_show = 5

header = vdomh.thead(
    vdomh.tr(
        vdomh.th("Motif ID", style={"text-align": "center"}),
        vdomh.th("q-val", style={"text-align": "center"}),
        vdomh.th("PWM", style={"text-align": "center"})
    )
)

for i in range(len(motif_pfms)):
    display(vdomh.h3("Metacluster %d/%d" % (i + 1, num_metaclusters)))
    
    # Compute TOMTOM matches for all motifs in the metacluster at once
    out_dir = os.path.join(tfm_motifs_cache_dir, "tomtom", "metacluster_%d" % i) if tfm_motifs_cache_dir else None
    tomtom_matches = match_motifs_to_database(motif_pfms_short[i], top_k=num_matches_to_keep, temp_dir=out_dir)
    
    for j in range(len(motif_pfms[i])):
        display(vdomh.h4("Motif %d/%d" % (j + 1, len(motif_pfms[i]))))
        viz_sequence.plot_weights(motif_hcwms[i][j])
    
        body = []
        for k, (match_name, match_pfm, match_qval) in enumerate(tomtom_matches[j]):
            fig = viz_sequence.plot_weights(pfm_to_pwm(match_pfm), return_fig=True)
            fig.tight_layout()
            if k < num_matches_to_show:
                body.append(
                    vdomh.tr(
                        vdomh.td(match_name),
                        vdomh.td(str(match_qval)),
                        vdomh.td(figure_to_vdom_image(fig))
                    )
                )
                if tfm_motifs_cache_dir:
                    # Save results and figures
                    motif_id = "%d_%d" % (i, j)
                    fig.savefig(os.path.join(out_dir, motif_id + ("_hit-%d.png" % (k + 1))))
            else:
                body.append(
                    vdomh.tr(
                        vdomh.td(match_name),
                        vdomh.td(str(match_qval)),
                        vdomh.td("Not shown")
                    )
                )
        if not body:
            display(vdomh.p("No TOMTOM matches passing threshold"))
        else:
            display(vdomh.table(header, vdomh.tbody(*body)))
        plt.close("all")

Metacluster 1/1

Motif 1/6

Motif IDq-valPWM
MA0059.1_MAX::MYC0.000890741
MXI1_HUMAN.H11MO.0.A0.000890741
MA0147.3_MYC0.000890741
MYCN_HUMAN.H11MO.0.A0.000890741
MXI1_HUMAN.H11MO.1.A0.000890741
MA0058.3_MAX0.000890741Not shown
MAX_HUMAN.H11MO.0.A0.000890741Not shown
MYC_HUMAN.H11MO.0.A0.000890741Not shown
MA0825.1_MNT0.00177129Not shown
MA0104.4_MYCN0.00350399Not shown

Motif 2/6

Motif IDq-valPWM
MA0471.2_E2F62.85995e-06
E2F1_HUMAN.H11MO.0.A2.85995e-06
E2F4_HUMAN.H11MO.0.A1.57863e-05
E2F3_HUMAN.H11MO.0.A1.77639e-05
E2F6_HUMAN.H11MO.0.A2.3685199999999998e-05
TFDP1_HUMAN.H11MO.0.C2.3685199999999998e-05Not shown
E2F7_HUMAN.H11MO.0.B0.000307642Not shown
MA1122.1_TFDP10.000858347Not shown
MA0865.1_E2F80.0146238Not shown
E2F4_HUMAN.H11MO.1.A0.0158618Not shown

Motif 3/6

Motif IDq-valPWM
MAX_HUMAN.H11MO.0.A0.183087
MA0058.3_MAX0.183087
MA0825.1_MNT0.183087
MA0632.2_TCFL50.183087
MA0147.3_MYC0.183087
MXI1_HUMAN.H11MO.1.A0.183087Not shown
MYC_HUMAN.H11MO.0.A0.183087Not shown
MA1099.2_HES10.230927Not shown
MA0506.1_NRF10.236625Not shown
MA0863.1_MTF10.236625Not shown

Motif 4/6

Motif IDq-valPWM
MA0147.3_MYC0.0837049
MYCN_HUMAN.H11MO.0.A0.0935243
MA0104.4_MYCN0.158634
MYC_HUMAN.H11MO.0.A0.185605
ZIC3_HUMAN.H11MO.0.B0.185605
HES1_HUMAN.H11MO.0.D0.185605Not shown
ZIC2_HUMAN.H11MO.0.D0.185605Not shown
MA0871.2_TFEC0.255271Not shown
HEY2_HUMAN.H11MO.0.D0.255271Not shown
MXI1_HUMAN.H11MO.0.A0.293175Not shown

Motif 5/6

Motif IDq-valPWM
CTCFL_HUMAN.H11MO.0.A4.2889699999999996e-10
CTCF_HUMAN.H11MO.0.A2.28237e-09
MA0139.1_CTCF7.7375e-08
MA1102.2_CTCFL2.45687e-06
SNAI1_HUMAN.H11MO.0.C0.0582889
MA0830.2_TCF40.0582889Not shown
MA1648.1_TCF12(var.2)0.07985419999999999Not shown
KLF8_HUMAN.H11MO.0.C0.07985419999999999Not shown
PLAL1_HUMAN.H11MO.0.D0.0879456Not shown
MA0147.3_MYC0.10588Not shown

Motif 6/6

Motif IDq-valPWM
MA0801.1_MGA0.00017196
MA1566.1_TBX30.00017196
MA1567.1_TBX60.00017196
MA1565.1_TBX180.00017196
MA0803.1_TBX150.00017196
MA0805.1_TBX10.00017196Not shown
MA0689.1_TBX200.000330063Not shown
MA0806.1_TBX40.000391735Not shown
MA0807.1_TBX50.0007350869999999999Not shown
MA0690.1_TBX210.00153575Not shown