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_fold9/E2F6_multitask_profile_fold9_imp_scores.h5
TF-MoDISco results path: /users/amtseng/tfmodisco/results/tfmodisco/multitask_profile/E2F6_multitask_profile_fold9/E2F6_multitask_profile_fold9_profile_tfm.h5
Importance score key: profile_hyp_scores
Saved TF-MoDISco-derived motifs cache: /users/amtseng/tfmodisco/results/reports/tfmodisco_results//cache/multitask_profile/E2F6_multitask_profile_fold9/E2F6_multitask_profile_fold9_profile
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 [00:28<00:00,  1.82it/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 1/2

Pattern 1/6

3768 seqlets

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

Pattern 2/6

3103 seqlets

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

Pattern 3/6

2703 seqlets

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

Pattern 4/6

2361 seqlets

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

Pattern 5/6

63 seqlets

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

Pattern 6/6

31 seqlets

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

Metacluster 2/2

Pattern 1/1

37 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 1/2

#SeqletsForwardReverse
13768
23103
32703
42361
563
631

Metacluster 2/2

#SeqletsForwardReverse
137

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 1/2

Motif 1/6

Motif IDq-valPWM
MA0147.3_MYC0.00020456400000000002
MAX_HUMAN.H11MO.0.A0.000291449
MXI1_HUMAN.H11MO.1.A0.0026009
MYC_HUMAN.H11MO.0.A0.00376005
MA0058.3_MAX0.00425921
MA0059.1_MAX::MYC0.00473245Not shown
MXI1_HUMAN.H11MO.0.A0.00655861Not shown
MA0004.1_Arnt0.00655861Not shown
MA0825.1_MNT0.0081006Not shown
MYCN_HUMAN.H11MO.0.A0.0176274Not shown

Motif 2/6

Motif IDq-valPWM
E2F1_HUMAN.H11MO.0.A0.000220285
MA0471.2_E2F60.00031376900000000004
E2F3_HUMAN.H11MO.0.A0.00031785200000000003
MA0865.1_E2F80.00046108
E2F6_HUMAN.H11MO.0.A0.00046108
E2F4_HUMAN.H11MO.1.A0.00046108Not shown
TFDP1_HUMAN.H11MO.0.C0.00046108Not shown
E2F4_HUMAN.H11MO.0.A0.000640785Not shown
MA0758.1_E2F70.000664517Not shown
E2F7_HUMAN.H11MO.0.B0.00119504Not shown

Motif 3/6

Motif IDq-valPWM
MA0632.2_TCFL50.149642
HES7_HUMAN.H11MO.0.D0.149642
MA0006.1_Ahr::Arnt0.149642
MYC_HUMAN.H11MO.0.A0.149642
MA0259.1_ARNT::HIF1A0.149642
MXI1_HUMAN.H11MO.1.A0.149642Not shown
MA0616.2_HES20.149642Not shown
MA0822.1_HES70.149642Not shown
MAX_HUMAN.H11MO.0.A0.149642Not shown
MA1560.1_SOHLH20.149642Not shown

Motif 4/6

No TOMTOM matches passing threshold

Motif 5/6

Motif IDq-valPWM
CPEB1_HUMAN.H11MO.0.D2.82842e-05
MA1125.1_ZNF3840.0286089
PRDM6_HUMAN.H11MO.0.C0.0288337
FOXL1_HUMAN.H11MO.0.D0.0288337
FOXG1_HUMAN.H11MO.0.D0.0591672
MA0679.2_ONECUT10.101643Not shown
FOXJ3_HUMAN.H11MO.0.A0.110849Not shown
ANDR_HUMAN.H11MO.0.A0.110849Not shown
HXC10_HUMAN.H11MO.0.D0.128666Not shown
ONEC2_HUMAN.H11MO.0.D0.191234Not shown

Motif 6/6

Motif IDq-valPWM
TBX15_HUMAN.H11MO.0.D6.3464e-08
MAZ_HUMAN.H11MO.0.A2.79232e-07
KLF16_HUMAN.H11MO.0.D3.04837e-07
ZN467_HUMAN.H11MO.0.C3.39811e-07
SP1_HUMAN.H11MO.0.A3.39811e-07
SP2_HUMAN.H11MO.0.A3.39811e-07Not shown
PATZ1_HUMAN.H11MO.0.C8.69765e-07Not shown
VEZF1_HUMAN.H11MO.0.C8.69765e-07Not shown
SP3_HUMAN.H11MO.0.B1.00619e-06Not shown
WT1_HUMAN.H11MO.0.C1.47934e-06Not shown

Metacluster 2/2

Motif 1/1

Motif IDq-valPWM
MXI1_HUMAN.H11MO.0.A0.00480133
ZN335_HUMAN.H11MO.0.A0.00796652
MAX_HUMAN.H11MO.0.A0.00796652
MA0058.3_MAX0.00796652
MA1099.2_HES10.00796652
MA0104.4_MYCN0.00796652Not shown
MA0616.2_HES20.00796652Not shown
MYC_HUMAN.H11MO.0.A0.00796652Not shown
MA0004.1_Arnt0.00796652Not shown
MA0823.1_HEY10.00796652Not shown