コード例 #1
0
ファイル: xdf.py プロジェクト: neuromti/tool-offspect
def prepare_annotations(
    xdffile: FileName,
    channel: str,
    pre_in_ms: float,
    post_in_ms: float,
    xmlfile: FileName = None,
    event_stream: str = "localite_marker",
    event_name: Union[str, int] = "coil_0_didt",
) -> Annotations:
    """load a documentation.txt and cnt-files and distill annotations from them
    
    args
    ----
    xdffile: FileName
        the :code:`.xdf`-file with the recorded streams, e.g. data and markers
    channel: str
        which channel to pick
    pre_in_ms: float
        how many ms to cut before the tms
    post_in_ms: float
        how many ms to cut after the tms

    returns
    -------
    annotation: Annotations
        the annotations for this origin files
    """
    stream_of_interest = channel  # rename to have same function signature
    streams = XDFFile(xdffile)
    if stream_of_interest in streams:
        datastream = streams[stream_of_interest]
    else:
        raise KeyError(
            f"Stream {stream_of_interest} was not found in the data")

    e_stream = streams[event_stream]
    time_stamps = [ts for ts in yield_timestamps(e_stream, event_name)]
    event_count = len(time_stamps)

    if "localite_flow" in streams or "localite_marker" in streams:
        loc_stream = streams["localite_marker"]
        coords = list(yield_loc_coords(loc_stream, time_stamps))
        stimulation_intensity_didt = list(
            yield_loc_didt(loc_stream, time_stamps))
        stimulation_intensity_mso = list(yield_loc_mso(loc_stream,
                                                       time_stamps))
    else:
        coords = list_nan_coords(event_count)
        stimulation_intensity_didt = list_nan(event_count)
        stimulation_intensity_mso = list_nan(event_count)
    print(f"Found {event_count} events")

    if "reiz_marker_sa" in streams:
        comments = [
            c for c in yield_comments(
                streams["reiz_marker_sa"],
                time_stamps=time_stamps,
                identifier="stimulus_idx",
                relative="earlier",
            )
        ]
    else:
        comments = ["" for c in time_stamps]

    # global fields
    fs = datastream.nominal_srate
    anno = AnnotationFactory(readin="tms",
                             readout="erp",
                             origin=Path(xdffile).name)
    anno.set("filedate", time.ctime(Path(xdffile).stat().st_mtime))
    anno.set("subject", "")  # TODO parse from somewhere
    anno.set("samplingrate", fs)
    anno.set("samples_pre_event", int(pre_in_ms * fs / 1000))
    anno.set("samples_post_event", int(post_in_ms * fs / 1000))
    anno.set("channel_of_interest", datastream.name)
    anno.set("channel_labels", datastream.channel_labels)
    # trace fields
    event_samples = find_closest_samples(datastream, time_stamps)
    event_times = [
        float(t) for t in datastream.time_stamps[event_samples] -
        datastream.time_stamps[0]
    ]
    time_since_last_pulse = [inf] + [
        a - b for a, b in zip(event_times[1:], event_times[0:-1])
    ]

    for idx in range(event_count):
        tattr = {
            "id": idx,
            "event_name": e_stream.name + "-" + str(event_name),
            "event_sample": event_samples[idx],
            "event_time": event_times[idx],
            "xyz_coords": coords[idx],
            "time_since_last_pulse_in_s": time_since_last_pulse[idx],
            "stimulation_intensity_mso": stimulation_intensity_mso[idx],
            "stimulation_intensity_didt": stimulation_intensity_didt[idx],
            "comment": comments[idx],
        }
        anno.append_trace_attr(tattr)
    return anno.anno
コード例 #2
0
ファイル: xdf.py プロジェクト: neuromti/tool-offspect
def prepare_annotations(
    xdffile: FileName,
    channel: str,
    pre_in_ms: float,
    post_in_ms: float,
    xmlfile: FileName = None,
    event_name="coil_0_didt",
    event_stream="localite_marker",
    comment_name=None,
) -> Annotations:
    """load a documentation.txt and cnt-files and distill annotations from them
    
    args
    ----
    xmlfile: FileName
        an option xml file with information about the target coordinates 

    readout: str
        which readout to use
    channel: str
        which channel to pick
    pre_in_ms: float
        how many ms to cut before the tms
    post_in_ms: float
        how many ms to cut after the tms
    xdffile: FileName
        the :code:`.xdf`-file with the recorded streams, e.g. data and markers
    returns
    -------
    annotation: Annotations
        the annotations for this origin files
    """

    # ------------------
    streams = XDFFile(xdffile)
    datastream = pick_stream_with_channel(channel, streams)
    event_stream = streams[event_stream]
    print(f"Reading events from {event_stream.name} using {event_name}")
    time_stamps = [ts for ts in yield_timestamps(event_stream, event_name)]
    event_count = len(time_stamps)
    print(f"Found {event_count} events")

    if "localite_flow" in streams or "localite_marker" in streams:
        loc_stream = streams["localite_marker"]
        print(f"Reading information from {loc_stream.name}")
        coords = list(yield_loc_coords(loc_stream, time_stamps))
        stimulation_intensity_didt = list(yield_loc_didt(loc_stream, time_stamps))
        stimulation_intensity_mso = list(yield_loc_mso(loc_stream, time_stamps))
    else:
        coords = list_nan_coords(event_count)
        stimulation_intensity_didt = list_nan(event_count)
        stimulation_intensity_mso = list_nan(event_count)

    if "reiz_marker_sa" in streams and comment_name is not None:
        print("Reading comments from reiz_marker_sa")
        comments = [
            c
            for c in yield_comments(
                streams["reiz_marker_sa"],
                time_stamps=time_stamps,
                identifier="stimulus_idx",
                relative="earlier",
            )
        ]
    else:
        comments = ["" for c in time_stamps]

    if "BrainVision RDA Markers" in streams:
        rda_stamps = list(yield_timestamps(streams["BrainVision RDA Markers"], "S  2"))
        print(f"Found {len(rda_stamps)} 'S  2' for {event_count} events")
        if len(rda_stamps) >= len(time_stamps):
            time_stamps = [find_closest(ts, rda_stamps) for ts in time_stamps]
            print("Corrected event timestamps for RDA 'S  2'")
        else:
            print("Count mismatch between RDA and Localite events")

        if "BrainVision RDA" in streams:
            bvr = streams["BrainVision RDA"]
            time_stamps = correct_tkeo(bvr, time_stamps)
            print("Corrected event timestamps for TMS artifact")

    # global fields
    fs = datastream.nominal_srate
    anno = AnnotationFactory(readin="tms", readout="cmep", origin=Path(xdffile).name)
    anno.set("filedate", time.ctime(Path(xdffile).stat().st_mtime))
    anno.set("subject", "")  # TODO parse from correctly organized file
    anno.set("samplingrate", fs)
    anno.set("samples_pre_event", int(pre_in_ms * fs / 1000))
    anno.set("samples_post_event", int(post_in_ms * fs / 1000))
    anno.set("channel_of_interest", channel)
    anno.set("channel_labels", [channel])
    # trace fields
    event_samples = find_closest_samples(datastream, time_stamps)
    event_times = [
        float(t)
        for t in datastream.time_stamps[event_samples] - datastream.time_stamps[0]
    ]
    time_since_last_pulse = [inf] + [
        a - b for a, b in zip(event_times[1:], event_times[0:-1])
    ]

    for idx, t in enumerate(event_samples):
        tattr = {
            "id": idx,
            "event_name": event_stream.name + "-" + str(event_name),
            "event_sample": event_samples[idx],
            "event_time": event_times[idx],
            "xyz_coords": coords[idx],
            "time_since_last_pulse_in_s": time_since_last_pulse[idx],
            "stimulation_intensity_mso": stimulation_intensity_mso[idx],
            "stimulation_intensity_didt": stimulation_intensity_didt[idx],
        }
        anno.append_trace_attr(tattr)
    return anno.anno
コード例 #3
0
def prepare_annotations_multfile(
    files,
    origin,
    filedate,
    channel: str,
    pre_in_ms: float,
    post_in_ms: float,
    comment_name=None,
):

    # we assume that all mapping was done after any spongebob assessments,
    # therefore everything earlier than the latest spongebob trigger is
    # considered irrelevant
    # alternatively, everything in an xdf-file earlier than a reiz_marker of
    # "" or earlier than any other marker is irrelevant. This is because every
    # start of a reiz-marker sends out an "" to see whether the marker-server
    # is running, while for all other assessments but mapping, the reiz-marker
    # was used to send markers

    for streams in files:
        if streams["reiz_marker_sa"].time_series[-1] == [""]:
            iu1 = 0
        else:
            iu1 = streams["reiz_marker_sa"].time_stamps[-1]

        spbob = np.where(streams["Spongebob-Data"].time_series[:,
                                                               11] == 1.0)[0]
        if len(spbob) == 0:  # we never triggered Spongebob in this file
            iu2 = 0
        else:
            idx = spbob[-1]
            iu2 = streams["Spongebob-Data"].time_stamps[idx]
        if max((iu1, iu2)) == 0:
            continue
        else:
            irrelevant_until = max((iu1, iu2))
        print(irrelevant_until)

    # we concatenate the time_series and time_stamps from the multiple xdf \
    # files. Because the clock is continuous and monotonic, we do not need to
    # correct for any possible reset between xdf files, and gaps are jumped
    # later
    time_stamps = []
    data_series = None
    data_stamps = None
    for streams in files:
        datastream = pick_stream_with_channel(channel, streams)
        if data_series is None:
            data_series = datastream.time_series
            data_stamps = datastream.time_stamps
        else:
            data_series = np.concatenate((data_series, datastream.time_series),
                                         axis=0)
            data_stamps = np.concatenate((data_stamps, datastream.time_stamps),
                                         axis=0)

        for event in streams["BrainVision RDA Markers"].time_stamps:
            if event > irrelevant_until:
                time_stamps.append(event)

    event_count = len(time_stamps)
    coords = list_nan_coords(event_count)
    stimulation_intensity_didt = list_nan(event_count)
    stimulation_intensity_mso = list_nan(event_count)
    print(f"Found {event_count} events")
    if event_count == 350:
        grid_layout = "5x7"
        print("This corresponds to a subject with a 5x7 grid")
    elif event_count == 360:
        grid_layout = "6x6"
        print("This corresponds to a subject with a 6x6 grid")
    else:
        grid_layout = "Unknown"
        print("This does not correspond to a known grid layout")

    # global fields
    fs = datastream.nominal_srate
    anno = AnnotationFactory(readin="tms", readout="cmep", origin=origin)
    anno.set("filedate", filedate)
    anno.set("subject", "")  # TODO parse from correctly organized file
    anno.set("samplingrate", fs)
    anno.set("samples_pre_event", int(pre_in_ms * fs / 1000))
    anno.set("samples_post_event", int(post_in_ms * fs / 1000))
    anno.set("channel_of_interest", channel)
    anno.set("channel_labels", [channel])
    anno.set("global_comment", f"grid_layout={grid_layout}")
    # trace fields
    event_samples = []
    for ts in time_stamps:
        idx = int(np.argmin(np.abs(data_stamps - ts)))
        event_samples.append(idx)

    #  New Implementation
    # gmfp = np.std(data_series[:, 0:64], 1)
    # artifact = tkeo(gmfp)
    # aptp = []
    # tp = []
    # for onset in event_samples:
    #     hood = gmfp[onset - 50 : onset + 50]
    #     aptp.append(np.max(hood))
    #     tp.append(int(np.argmax(hood) - 50 + onset))
    # event_samples = tp

    gmfp = np.std(data_series[:, 0:64], 1)
    aptp = []
    tp = []
    for onset in event_samples:
        artifact = gmfp[onset - 25:onset + 25]
        aptp.append(np.ptp(artifact))
        tp.append(int(np.argmax(artifact) - 25 + onset))
    event_samples = tp

    event_times = [
        float(t) for t in data_stamps[event_samples] - data_stamps[0]
    ]
    time_since_last_pulse = [inf] + [
        a - b for a, b in zip(event_times[1:], event_times[0:-1])
    ]
    for idx, t in enumerate(event_samples):
        tattr = {
            "id": idx,
            "comment": f'{{"artifact_amplitude":{aptp[idx]:3.2f}}}',
            "event_name": "BrainVision RDA Markers - 'S  2'",
            "event_sample": event_samples[idx],
            "event_time": event_times[idx],
            "xyz_coords": coords[idx],
            "time_since_last_pulse_in_s": time_since_last_pulse[idx],
            "stimulation_intensity_mso": stimulation_intensity_mso[idx],
            "stimulation_intensity_didt": stimulation_intensity_didt[idx],
        }
        anno.append_trace_attr(tattr)
    return anno.anno
コード例 #4
0
def prepare_annotations(
    streams,
    origin,
    filedate,
    channel: str,
    pre_in_ms: float,
    post_in_ms: float,
    comment_name=None,
) -> Annotations:
    """load a documentation.txt and cnt-files and distill annotations from them
    
    args
    ----
    xmlfile: FileName
        an option xml file with information about the target coordinates 

    readout: str
        which readout to use
    channel: str
        which channel to pick
    pre_in_ms: float
        how many ms to cut before the tms
    post_in_ms: float
        how many ms to cut after the tms
    xdffile: FileName
        the :code:`.xdf`-file with the recorded streams, e.g. data and markers
    returns
    -------
    annotation: Annotations
        the annotations for this origin files
    """

    # ------------------

    datastream = pick_stream_with_channel(channel, streams)

    iu1 = streams["reiz_marker_sa"].time_stamps[-1]
    idx = np.where(streams["Spongebob-Data"].time_series[:, 11] == 1.0)[0][-1]
    iu2 = streams["Spongebob-Data"].time_stamps[idx]
    irrelevant_until = max((iu1, iu2))

    time_stamps = []
    for event in streams["BrainVision RDA Markers"].time_stamps:
        if event > irrelevant_until:
            time_stamps.append(event)

    event_count = len(time_stamps)

    coords = list_nan_coords(event_count)
    stimulation_intensity_didt = list_nan(event_count)
    stimulation_intensity_mso = list_nan(event_count)
    comments = ["" for c in time_stamps]
    print(f"Found {event_count} events")
    if event_count == 350:
        grid_layout = "5x7"
        print("This corresponds to a subject with a 5x7 grid")
    elif event_count == 360:
        grid_layout = "6x6"
        print("This corresponds to a subject with a 6x6 grid")
    else:
        grid_layout = "Unknown"
        print("This does not correspond to a known grid layout")

    # global fields
    fs = datastream.nominal_srate
    anno = AnnotationFactory(readin="tms", readout="cmep", origin=origin)
    anno.set("filedate", filedate)
    anno.set("subject", "")  # TODO parse from correctly organized file
    anno.set("samplingrate", fs)
    anno.set("samples_pre_event", int(pre_in_ms * fs / 1000))
    anno.set("samples_post_event", int(post_in_ms * fs / 1000))
    anno.set("channel_of_interest", channel)
    anno.set("channel_labels", [channel])
    anno.set("global_comment", f"grid_layout={grid_layout}")
    # trace fields
    event_samples = find_closest_samples(datastream, time_stamps)

    # shift onset on Peak of artifact
    ephys = streams["BrainVision RDA"]
    gmfp = np.std(ephys.time_series[:, 0:64], 1)
    aptp = []
    tp = []
    for onset in event_samples:
        artifact = gmfp[onset - 25:onset + 25]
        aptp.append(np.ptp(artifact))
        tp.append(int(np.argmax(artifact) - 25 + onset))
    event_samples = tp

    event_times = [
        float(t) for t in datastream.time_stamps[event_samples] -
        datastream.time_stamps[0]
    ]
    time_since_last_pulse = [inf] + [
        a - b for a, b in zip(event_times[1:], event_times[0:-1])
    ]
    for idx, t in enumerate(event_samples):
        tattr = {
            "id": idx,
            "comment": f'{{"artifact_amplitude":{aptp[idx]:3.2f}}}',
            "event_name": "BrainVision RDA Markers - 'S  2'",
            "event_sample": event_samples[idx],
            "event_time": event_times[idx],
            "xyz_coords": coords[idx],
            "time_since_last_pulse_in_s": time_since_last_pulse[idx],
            "stimulation_intensity_mso": stimulation_intensity_mso[idx],
            "stimulation_intensity_didt": stimulation_intensity_didt[idx],
        }
        anno.append_trace_attr(tattr)
    return anno.anno
コード例 #5
0
def prepare_annotations_multifile(
    files,
    origin,
    filedate,
    channel: str,
    pre_in_ms: float,
    post_in_ms: float,
    comment_name=None,
):

    # we assume that all mapping was done after any spongebob assessments,
    # therefore everything earlier than the latest spongebob trigger is
    # considered irrelevant
    # alternatively, everything in an xdf-file earlier than a reiz_marker of
    # "" or earlier than any other marker is irrelevant. This is because every
    # start of a reiz-marker sends out an "" to see whether the marker-server
    # is running, while for all other assessments but mapping, the reiz-marker
    # was used to send markers

    for streams in files:
        if streams["reiz_marker_sa"].time_series[-1] == [""]:
            iu1 = 0
        else:
            iu1 = streams["reiz_marker_sa"].time_stamps[-1]

        spbob = np.where(streams["Spongebob-Data"].time_series[:,
                                                               11] == 1.0)[0]
        if len(spbob) == 0:  # we never triggered Spongebob in this file
            iu2 = 0
        else:
            idx = spbob[-1]
            iu2 = streams["Spongebob-Data"].time_stamps[idx]

        if iu1 > iu2:
            print(
                "WARNING: Spongebob data was not transmitted after NMES-IOC. Possible reason: Death of Outlet?"
            )
        else:
            print("Spongebob data was transmitted after NMES-IOC")
        if max((iu1, iu2)) == 0:
            continue
        else:
            irrelevant_until = max((iu1, iu2))
        print(irrelevant_until)

    # we concatenate the time_series and time_stamps from the multiple xdf \
    # files. Because the clock is continuous and monotonic, we do not need to
    # correct for any possible reset between xdf files, and gaps are jumped
    # later
    time_stamps = []
    data_series = None
    data_stamps = None
    for streams in files:
        datastream = pick_stream_with_channel(channel, streams)
        if data_series is None:
            data_series = datastream.time_series
            data_stamps = datastream.time_stamps
        else:
            data_series = np.concatenate((data_series, datastream.time_series),
                                         axis=0)
            data_stamps = np.concatenate((data_stamps, datastream.time_stamps),
                                         axis=0)

        for event in streams["BrainVision RDA Markers"].time_stamps:
            if event > irrelevant_until:
                time_stamps.append(event)

    event_count = len(time_stamps)
    coords = list_nan_coords(event_count)
    stimulation_intensity_didt = list_nan(event_count)
    stimulation_intensity_mso = list_nan(event_count)
    print(f"Found {event_count} events")
    if event_count == 350:
        grid_layout = "5x7"
        print("This corresponds to a subject with a 5x7 grid")
    elif event_count == 360:
        grid_layout = "6x6"
        print("This corresponds to a subject with a 6x6 grid")
    else:
        grid_layout = "Unknown"
        print("This does not correspond to a known grid layout")

    # global fields
    fs = datastream.nominal_srate
    anno = AnnotationFactory(readin="tms", readout="cmep", origin=origin)
    anno.set("filedate", filedate)
    anno.set("subject", "")  # TODO parse from correctly organized file
    anno.set("samplingrate", fs)
    anno.set("samples_pre_event", int(pre_in_ms * fs / 1000))
    anno.set("samples_post_event", int(post_in_ms * fs / 1000))
    anno.set("channel_of_interest", channel)
    anno.set("channel_labels", [channel])
    anno.set("global_comment", f"grid_layout={grid_layout}")
    # trace fields
    event_samples = []
    for ts in time_stamps:
        idx = int(np.argmin(np.abs(data_stamps - ts)))
        event_samples.append(idx)

    #  New Implementation
    # gmfp = np.std(data_series[:, 0:64], 1)
    # artifact = tkeo(gmfp)
    # aptp = []
    # tp = []
    # for onset in event_samples:
    #     hood = gmfp[onset - 50 : onset + 50]
    #     aptp.append(np.max(hood))
    #     tp.append(int(np.argmax(hood) - 50 + onset))
    # event_samples = tp

    gmfp = np.std(data_series[:, 0:64], 1)
    aptp = []
    tp = []
    for onset in event_samples:
        artifact = gmfp[onset - 25:onset + 25]
        aptp.append(np.ptp(artifact))
        tp.append(int(np.argmax(artifact) - 25 + onset))
    event_samples = tp

    event_times = [
        float(t) for t in data_stamps[event_samples] - data_stamps[0]
    ]
    time_since_last_pulse = [inf] + [
        a - b for a, b in zip(event_times[1:], event_times[0:-1])
    ]

    # sometimes, we record way too many pulses for a mapping

    max_allowed_counts = int(360 * 1.2)
    if event_count > max_allowed_counts:
        print(
            "WARNING: There are too many pulses, throwing away possible faulty ones"
        )
        template = np.ones(180)
        template[0::5] = 1.5
        template[0] = 100

        selection = []
        old_xcorr = 0
        new_xcorr = 0
        to = 1
        fr = 181
        while fr < max_allowed_counts:
            new_xcorr = np.correlate(time_since_last_pulse[-fr:-to], template)
            print(fr, to, new_xcorr)
            if new_xcorr < old_xcorr / 2:
                # the last was a good fit, at least twice better than now
                winner = (fr - 1, to - 1)
                selection.extend(list(range(to + 1, fr + 1)))
                fr += 180
                to += 180
                old_xcorr = 0
                new_xcorr = 0
                print("We found a winner", winner)

            else:
                old_xcorr = new_xcorr
                fr += 1
                to += 1
        if len(selection) != 720:
            raise Exception("Did not find a good selection of good events")

        event_samples = drop_selection(event_samples, selection)
        event_times = drop_selection(event_times, selection)
        coords = drop_selection(coords, selection)
        time_since_last_pulse = drop_selection(time_since_last_pulse,
                                               selection)
        stimulation_intensity_mso = drop_selection(stimulation_intensity_mso,
                                                   selection)
        stimulation_intensity_didt = drop_selection(stimulation_intensity_didt,
                                                    selection)
        aptp = drop_selection(aptp, selection)

    for idx, t in enumerate(event_samples):
        tattr = {
            "id": idx,
            "comment": f'{{"artifact_amplitude":{aptp[idx]:3.2f}}}',
            "event_name": "BrainVision RDA Markers - 'S  2'",
            "event_sample": event_samples[idx],
            "event_time": event_times[idx],
            "xyz_coords": coords[idx],
            "time_since_last_pulse_in_s": time_since_last_pulse[idx],
            "stimulation_intensity_mso": stimulation_intensity_mso[idx],
            "stimulation_intensity_didt": stimulation_intensity_didt[idx],
        }
        anno.append_trace_attr(tattr)
    return anno.anno