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: MAX
DeepSHAP scores path: /users/amtseng/tfmodisco/results/importance_scores/multitask_profile/MAX_multitask_profile_fold4/MAX_multitask_profile_fold4_imp_scores.h5
TF-MoDISco results path: /users/amtseng/tfmodisco/results/tfmodisco/multitask_profile/MAX_multitask_profile_fold4/MAX_multitask_profile_fold4_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/MAX_multitask_profile_fold4/MAX_multitask_profile_fold4_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%|██████████| 204/204 [01:41<00:00,  2.00it/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 1/5

6197 seqlets

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

Pattern 2/5

4204 seqlets

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

Pattern 3/5

583 seqlets

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

Pattern 4/5

146 seqlets

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

Pattern 5/5

44 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
16197
24204
3583
4146
544

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 1/5

Motif IDq-valPWM
MYCN_HUMAN.H11MO.0.A0.00195173
MA0104.4_MYCN0.00195912
MA0059.1_MAX::MYC0.00213617
CR3L1_HUMAN.H11MO.0.D0.0077406
MXI1_HUMAN.H11MO.0.A0.0077406
MXI1_HUMAN.H11MO.1.A0.00779917Not shown
MAX_HUMAN.H11MO.0.A0.00779917Not shown
MYC_HUMAN.H11MO.0.A0.00779917Not shown
MA0004.1_Arnt0.00936121Not shown
MA0058.3_MAX0.00936121Not shown

Motif 2/5

Motif IDq-valPWM
MA1650.1_ZBTB140.0035508000000000002
MA1513.1_KLF150.019177200000000002
MA0147.3_MYC0.019177200000000002
SP1_HUMAN.H11MO.1.A0.028669299999999998
SP3_HUMAN.H11MO.0.B0.0286743
MA0741.1_KLF160.0286743Not shown
MA0746.2_SP30.0286743Not shown
MA0104.4_MYCN0.029172700000000003Not shown
MA1099.2_HES10.029172700000000003Not shown
KLF9_HUMAN.H11MO.0.C0.0308313Not shown

Motif 3/5

Motif IDq-valPWM
CTCF_HUMAN.H11MO.0.A0.000726572
MA0139.1_CTCF0.00105483
CTCFL_HUMAN.H11MO.0.A0.0012745999999999999
MA1102.2_CTCFL0.0271944
SNAI1_HUMAN.H11MO.0.C0.0271944
MA0748.2_YY20.0965333Not shown
PLAG1_HUMAN.H11MO.0.D0.100102Not shown
ZFX_HUMAN.H11MO.0.A0.107852Not shown
MA0830.2_TCF40.107852Not shown
AP2B_HUMAN.H11MO.0.B0.107852Not shown

Motif 4/5

Motif IDq-valPWM
MXI1_HUMAN.H11MO.0.A0.0270454
CTCF_HUMAN.H11MO.0.A0.0270454
MA0104.4_MYCN0.0270454
CTCFL_HUMAN.H11MO.0.A0.033077499999999996
USF2_HUMAN.H11MO.0.A0.038790899999999996
SP1_HUMAN.H11MO.0.A0.041841500000000004Not shown
CR3L1_HUMAN.H11MO.0.D0.0477297Not shown
MA0139.1_CTCF0.0477297Not shown
MA0748.2_YY20.0803552Not shown
MA0814.2_TFAP2C(var.2)0.0803552Not shown

Motif 5/5

Motif IDq-valPWM
ZN770_HUMAN.H11MO.0.C5.41419e-07
MA1596.1_ZNF4600.022672799999999996
RARA_HUMAN.H11MO.0.A0.022780900000000003
ZN770_HUMAN.H11MO.1.C0.0306887
RARB_HUMAN.H11MO.0.D0.0351836
ZN219_HUMAN.H11MO.0.D0.0351836Not shown
MA1587.1_ZNF1350.0433017Not shown
ZFX_HUMAN.H11MO.1.A0.0611371Not shown
PAX5_HUMAN.H11MO.0.A0.11552Not shown
MA1531.1_NR1D10.11552Not shown