forna.py

#!/usr/bin/python

"""forna.py: A script for converting RNA secondary structure to json objects encoding
   a graph to be visualized using d3.js's force-directed graph layout."""

__author__ = "Peter Kerpedjiev"
__copyright__ = "Copyright 2014"
__version__ = "0.1"
__maintainer__ = "Peter Kerpedjiev"
__email__ = "pkerp@tbi.univie.ac.at"

import forgi.graph.bulge_graph as fgb
import forgi.threedee.utilities.pdb as ftup
import forgi.threedee.model.coarse_grain as ftmc
import forgi.utilities.debug as fud

import Bio.PDB as bpdb
import collections as col
import itertools as it
import json
import math
import numpy as np
import os.path as op
import RNA
import tempfile
import forgi.utilities.stuff as fus

import sys
from optparse import OptionParser


def remove_pseudoknots(bg):
    """
    Remove all pseudoknots from the structure and return a list
    of tuples indicate the nucleotide numbers which were in the
    pseudoknots.
    
    @param bg: The BulgeGraph structure
    """
    # store which base pairs we've dissolved
    dissolved_bp = []
    dissolved = True
    while dissolved:
        dissolved = False
        # keep iterating as long as we've dissolved a stem
        for d in bg.mloop_iterator():
            if bg.is_node_pseudoknot(d):
                # does this multiloop lead to a pseudoknot?
                # if so, one of the stems it connects needs to be unravelled
                conn = bg.connections(d)
                conn_len = [(bg.stem_length(c), c) for c in conn]
                conn_len.sort()
                to_dissolve = conn_len[0][1]

                dissolved_bp += list(bg.stem_bp_iterator(to_dissolve))
                bg.dissolve_stem(conn_len[0][1])
                dissolved = True
                break

    return dissolved_bp


def bg_to_json(bg, circular=False):
    """
    Convert a BulgeGraph to a json file containing a graph layout designed
    to create a nice force-directed graph using the d3 library.
    """

    # the json structure that will hold everything
    struct = {"nodes": [], "links": []}

    # the initial width and height of the screen
    scr_width = 800.
    scr_height = 600.

    # pseudoknot_pairs = []
    pseudoknot_pairs = bg.remove_pseudoknots()

    # the X and Y coordinates of each nucleotide as returned by RNAplot
    bp_string = bg.to_dotbracket_string()
    coords = RNA.get_xy_coordinates(bp_string)
    xs = np.array([coords.get(i).X for i in range(bg.seq_length)])
    ys = np.array([coords.get(i).Y for i in range(bg.seq_length)])

    # center the structure on the screen
    center_x = np.mean(xs)
    center_y = np.mean(ys)

    center_width = scr_width / 2.
    center_height = scr_height / 2.

    new_xs = (xs - center_x) + center_width
    new_ys = (ys - center_y) + center_height

    # corresponds to the colors in d3's category10 color scale
    colors = {'s': 'lightgreen', 'm': '#ff9896', 'i': '#dbdb8d', 'f': 'lightsalmon', 't': 'lightcyan', 'h': 'lightblue',
              'x': 'transparent'}

    for (f, t) in pseudoknot_pairs:
        struct["links"] += [{"source": f - 1, "target": t - 1, "value": 1, "link_type": "pseudoknot"}]

    for i in range(bg.seq_length):
        # use the centered coordinates for each nucleotide
        x = new_xs[i]
        y = new_ys[i]

        # create the nodes with initial positions
        # the  node_name comes from the forgi representation
        node_name = bg.get_node_from_residue_num(i + 1)
        node = {"group": 1, "elem": node_name, "elem_type": node_name[0], "name": bg.seq[i], "id": i + 1,
                "x": x, "y": y, "px": x, "py": y, "color": colors[node_name[0]],
                "node_type": "nucleotide", 'struct_name': bg.name}

        # node = {"group": 1, "name": i+1, "id": i+1}
        struct["nodes"] += [node]

        # link adjacent nodes
        # the numbers for source and target indicate the indices of the nodes
        # in the "nodes" array, not their id or name
        if 0 < i < bg.seq_length:
            link = {"source": i - 1, "target": i, "value": 1, "link_type": "real"}
            struct["links"] += [link]

    if circular:
        struct["links"] += [{"source": 0, "target": bg.seq_length-1, "value":1, "link_type": "real"}]

    num_nodes = len(struct["nodes"])
    num_labels = 0
    for i in range(bg.seq_length):
        if (i + 1) % 10 == 0:
            node_id = num_nodes + num_labels
            num_labels += 1

            struct["nodes"] += [{"group": 1, "name": "{}".format(i + 1), "id": node_id,
                                 "color": 'transparent', 'node_type': 'label', "struct_name": bg.name}]
            struct["links"] += [{"source": i, "target": node_id, "value": 1, "link_type": "real"}]

    # store the node id of the center id for each loop
    centers_radii = dict()
    num_nodes = len(struct["nodes"])

    def create_loop_node(ds, res_list, node_id):
        """
        Create a pseudo-node in the middle of each loop. This node
        will be the center of the circular arrangement of the loop
        nodes.
        """
        # get the coordinates of the nodes which are part of this loop
        xs = np.array([coords.get(r).X for r in res_list])
        ys = np.array([coords.get(r).Y for r in res_list])

        # center them on the viewport
        x_pos = np.mean(xs) - center_x + center_width
        y_pos = np.mean(ys) - center_y + center_height

        # create a pseudo node for each of the loops
        struct["nodes"] += [{"group": 1, "name": "", "id": node_id,
                             "x": x_pos, "y": y_pos, "px": x_pos, "py": y_pos,
                             "color": colors['x'], 'node_type': 'pseudo', 'struct_name': bg.name}]

        # some geometric calculations for deciding how long to make
        # the links between alternating nodes
        num_residues = len(res_list)
        angle = (num_residues - 2) * math.pi / (2 * num_residues)
        width = 0.5 / math.cos(angle)

        for d in ds:
            centers_radii[d] = (node_id, width)

        for j, rn in enumerate(res_list):
            # link nodes to the center
            struct["links"] += [{"source": node_id, "target": rn - 1, "value": width, "link_type": "fake"}]

        for j in range(0, (num_residues + 1) / 2):
            # link nodes across the loop
            fri = j
            tri = (j + num_residues / 2)
            struct["links"] += [
                {"source": res_list[fri] - 1, "target": res_list[tri] - 1, "value": width * 2, "link_type": "fake"}]

        for j in range(0, num_residues, 1):
            # link every other node in the loop
            ia = ((num_residues - 2) * math.pi) / num_residues
            # a = math.pi/2 - ia/2.
            c = 2 * math.cos(math.pi / 2. - ia / 2.)
            fri = j
            tri = (j + 2) % num_residues
            struct["links"] += [
                {"source": res_list[fri] - 1, "target": res_list[tri] - 1, "value": c, "link_type": "fake"}]

    # Create the loop pseudo-nodes for hairpins and interior loops
    num_nodes = len(struct["nodes"])
    # pseudoknotted = [item for sublist in pseudoknot_pairs for item in sublist]
    pseudoknotted = []

    counter = 0
    for i, d in enumerate(it.chain(bg.iloop_iterator(),
                                   bg.hloop_iterator())):
        stop = False
        for dr in bg.define_residue_num_iterator(d, adjacent=True):
            if dr in pseudoknotted:
                # don't create loop nodes for pseudoknotted regions
                stop = True
        if stop:
            continue

        create_loop_node([d],
                         list(bg.define_residue_num_iterator(d, adjacent=True)),
                         num_nodes + counter)
        counter += 1

    # create the loop pseudo-nodes for multiloops

    num_nodes = len(struct["nodes"])
    counter = 0
    loops, residue_lists = bg.find_multiloop_loops()
    for loop, residue_list in zip(loops, residue_lists):
        loop_elems = [d for d in loop if d[0] == 'm']

        if bg.is_loop_pseudoknot(loop):
            # we shouldn't make a pseudonode for a psueodknotted node
            continue

        residue_list = sorted(residue_list)

        create_loop_node(loop_elems, residue_list, num_nodes + counter)
        counter += 1

    # create a common node for the external loop
    '''
    eloops = bg.find_external_loops()
    if len(eloops) > 0:
        all_residues = it.chain(*[bg.define_residue_num_iterator(e, adjacent=True) for e in eloops])
        create_loop_node(eloops, sorted(all_residues), len(struct["nodes"]))
    '''

    # link the nodes that are in stems
    for i in range(0, bg.seq_length - 2):
        if i + 1 in pseudoknotted or i + 2 in pseudoknotted or i + 3 in pseudoknotted:
            continue

        # create triangles between semi-adjacent nucleotides
        node1 = bg.get_node_from_residue_num(i + 1)
        #node15 = bg.get_node_from_residue_num(i+2)
        node2 = bg.get_node_from_residue_num(i + 3)

        def create_stem_loop_link(node1, node2):
            """
            Create a link between the second-to-last node on a stem
            and the second-to-last node on a loop.
            """
            res_list = list(bg.define_residue_num_iterator(node2, adjacent=True))
            num_residues = len(res_list)
            ia = ((num_residues - 2) * math.pi) / (num_residues)
            angle1 = 2 * math.pi - ia - math.pi / 2.
            angle2 = (math.pi - angle1) / 2.

            if math.sin(angle2) > 0.00001:
                x = math.sin(angle1) / math.sin(angle2)
            else:
                x = 2.

            struct["links"] += [{"source": i, "target": i + 2, "value": x, "link_type": "fake"}]

        # actually make the stem-loop links
        if node1[0] == 's' and node2[0] == 's' and node1 == node2:
            struct["links"] += [{"source": i, "target": i + 2, "value": 2, "link_type": "fake"}]

        """
        if (node1[0] == 's' and node15[0] == 's' and node2[0] != 's'):
            create_stem_loop_link(node1, node2)

        if (node1[0] != 's' and node15[0] == 's' and node2[0] == 's'):
            create_stem_loop_link(node2, node1)

            pass
        """

    # link paired nucleotides
    for d in bg.stem_iterator():
        prev_f, prev_t = None, None

        for (f, t) in bg.stem_bp_iterator(d):
            link = {"source": f - 1, "target": t - 1, "value": 1, "link_type": "real"}
            struct["links"] += [link]

            if prev_f is not None and prev_t is not None:
                struct["links"] += [
                    {"source": f - 1, "target": prev_t - 1, "value": 1 * math.sqrt(2), "link_type": "fake"}]
                struct["links"] += [
                    {"source": t - 1, "target": prev_f - 1, "value": 1 * math.sqrt(2), "link_type": "fake"}]

            prev_f, prev_t = f, t

    return struct


def fasta_to_json(fasta_text, circular=False):
    """
    Create the d3 compatible graph representation from a dotbracket string
    formatted like so:

        >id
        ACCCGGGG
        (((..)))

    @param fasta_text: The fasta string.
    """
    bg = fgb.BulgeGraph()
    bg.from_fasta(fasta_text)
    return bg_to_json(bg, circular=circular)


def parse_ranges(range_text):
    '''
    Parse a numerical range indicated like this:

    13-14,15,16-17

    And a return a sorted array containing the numbers
    covered by this range. Negative values are not
    allowed. Overlapping values will be counted only once.
    '''
    all_nucleotides = set()

    ranges = range_text.split(',')
    for single_range in ranges:
        if single_range.count('-') > 1:
            raise Exception('Too many dashes in the range')
        elif single_range.count('-') == 1:
            parts = single_range.split('-')
            if len(parts) != 2 or parts[0] == '' or parts[1] == '':
                raise Exception('Invalid range')

            try:
                (f,t) = map(int, single_range.split('-'))
            except ValueError as ve:
                raise Exception('Range components need to be integers')
        else:
            try:
                (f,t) = (int(single_range), int(single_range))
            except ValueError as ve:
                raise Exception('Range components need to be integers')

        for i in range(f,t+1):
            all_nucleotides.add(i)

    return sorted(all_nucleotides)
    
def parse_colors_text(colors_text):
    '''
    Parse a text string and return a json object which identifies
    the colors with which nucleotides should be colored.

    The colors lines should look like this:

    #color struct_name residue_num color_value
    color 1y26 13 red

    Nucleotide ranges can be specified using dashes:
    
    color 1y26 13-14 red

    Multiple nucleotides and/or ranges can be combined using commas:

    color 1y26 13-14,15 blue

    Highlights are specified in a similar manner, except the effect
    is that the convex hull of the nucleotides of each highlight are
    colored in the color specified.

    @param colors_text: A string containing the color specs
    @return: A json object indicating which nucleotides should 
             have which colors.
    '''
    # colors will be a dictionary indexed by molecule_name, and residue_id
    # 
    colors = col.defaultdict(col.defaultdict)

    for i,line in enumerate(colors_text.split('\n')):
        parts = line.split()

        if len(parts) == 0:
            # we'll let empty lines slide
            continue
        
        if len(parts) != 4:
            raise Exception('Too many parts in line {}'.format(i+1))

        if parts[0] == 'color':
            try: 
                nucleotides = parse_ranges(parts[2])
            except Exception as ex:
                raise Exception("Improperly formatted range on line {}: {}".format(i+1, str(ex)))

            color = parts[3]

            for nucleotide in nucleotides:
                #color_entry = {"name":parts[1], "nucleotide":nucleotide, "color":color}
                colors[parts[1]][nucleotide] = color
                #colors += [color_entry]

    return colors

def add_colors_to_graph(struct, colors):
    """
    Change the colors in the structure graph. Colors should be a dictionary-fied
    json object containing the following entries:

    [{'name': '1Y26_X', 'nucleotide':15, 'color':'black'}]
    
    @param struct: The structure returned by fasta_to_json
    @param colors: A color dictionary as specified above
    """
    for node in struct['nodes']:
        if node['node_type'] == 'nucleotide':
            if node['struct_name'] in colors:
                if node['id'] in colors[node['struct_name']]:
                    node['color'] = colors[node['struct_name']][node['id']]

    return struct


def main():
    usage = """
    python cg_to_d3_bp.py x.fa

    Create a json file specifying a d3 force-directed graph for this
    secondary structure. If the specified argument is '-', then the
    input is read from stdin.
    """
    num_args = 1
    parser = OptionParser(usage=usage)

    # parser.add_option('-o', '--options', dest='some_option', default='yo', help="Place holder for a real option",
    # type='str')
    # parser.add_option('-u', '--useless', dest='uselesss', default=False, action='store_true', help='Another useless
    #  option')
    parser.add_option('-c', '--colors', dest='colors', default=None,
                      help='Specifiy a json file which contains information about nucleotide colors',
                      type='str')

    (options, args) = parser.parse_args()

    if len(args) < num_args:
        parser.print_help()
        sys.exit(1)

    if args[0] == '-':
        text = sys.stdin.read()
    else:
        fname, fext = op.splitext(args[0])
        if fext == '.cg' or fext == '.bg':
            print >> sys.stderr, "Detected BulgeGraph"
            bg = fgb.BulgeGraph(args[0])
            struct = bg_to_json(bg)
        else:
            print >> sys.stderr, "Detected fasta"
            with open(args[0], 'r') as f:
                text = f.read()

    struct = fasta_to_json(text)

    if options.colors is not None:
        with open(options.colors) as f:
            colors = json.loads(f)
            struct = add_colors_to_graph(struct, colors)

    print json.dumps(struct, sort_keys=True, indent=4, separators=(',', ': '))


def pdb_to_json(text, name):
    '''
    Create a graph-layout displaying a pdb file which
    presumably contains some RNA

    The text is the contents of the pdb file.
    '''
    with fus.make_temp_directory() as output_dir:
        fname = op.join(output_dir, '{}.pdb'.format(name))

        with open(fname, 'w') as f:
            # dump the pdb text to a temporary file
            f.write(text)
            f.flush

            struct = bpdb.PDBParser().get_structure('temp', fname)
            chains = struct.get_chains()

        jsons = []

        proteins = set()
        rnas = set()

        cgs = dict()

        for chain in chains:
            # create a graph json for each structure in the pdb file
            if ftup.is_protein(chain):
                proteins.add(chain.id)
                # process protein
                jsons += [{"nodes":[{"group":2, 
                                     "struct_name": "{}_{}".format(name, chain.id),
                                     "id": 1,
                                     "size": len(chain.get_list()),
                                     "name": chain.id,
                                     "node_type":"protein"}],
                           "links":[]}]
                pass
            else:
                rnas.add(chain.id)
                # process RNA molecules (hopefully)
                cg = ftmc.from_pdb(fname, chain_id=chain.id)
                cgs[chain.id] = cg
                jsons += [bg_to_json(cg)]

        # create a lookup table to find out the index of each node in the 
        # what will eventually become the large list of nodes
        counter = 0
        node_ids = dict()
        for j in jsons:
            for n in j['nodes']:
                node_ids["{}_{}".format(n['struct_name'], n['id'])] = counter
                fud.pv('counter, n')
                counter += 1

        links = []
        for (a1, a2) in ftup.interchain_contacts(struct):
            #fud.pv('a1.parent.id[0]')
            if (a1.parent.id[0] != ' ' or a2.parent.id[0] != ' '):
                #hetatm's will be ignored for now
                continue

            chain1 = a1.parent.parent.id
            chain2 = a2.parent.parent.id

            # the source and target values below need to be reduced by the length of the
            # nodes array because when the jsons are added to the graph, the link
            # source and target are incremented so as to correspond to the new indeces
            # of the nodes
            # so a link to a node at position 10, if there are 50 nodes, will have to have
            # a source value of -40
            if (chain1 in proteins and chain2 in rnas):
                # get the index of this nucleotide in the secondary structure
                sid = cgs[chain2].seq_ids.index(a2.parent.id)

                links += [{"source": node_ids["{}_{}_{}".format(name, chain2, sid+1)] - counter,
                           "target": node_ids["{}_{}_{}".format(name, chain1, 1)] - counter,
                           "link_type": "protein_chain",
                           "value": 3}]
                fud.pv('links[-1]')
            elif (chain2 in proteins and chain1 in rnas):
                # get the index of this nucleotide in the secondary structure

                sid = cgs[chain1].seq_ids.index(a1.parent.id)

                links += [{"source": node_ids["{}_{}_{}".format(name, chain1, sid+1)] - counter,
                           "target": node_ids["{}_{}_{}".format(name, chain2, 1)] - counter,
                           "link_type": "protein_chain",
                           "value": 3}]
                fud.pv('links[-1]')

        #jsons += [{'nodes': [], "links": links}]
        jsons += [{"nodes": [], "links": links}]
        return {"jsons": jsons, "extra_links": links}

if __name__ == '__main__':
    main()