Spaces:
Running
on
Zero
Running
on
Zero
Anton Bushuiev
commited on
Commit
·
3401fbb
1
Parent(s):
575d08b
Fix retention time
Browse files- app.py +22 -20
- data/example_5_spectra.mgf +0 -350
app.py
CHANGED
@@ -264,7 +264,7 @@ def setup():
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('https://huggingface.co/datasets/roman-bushuiev/GeMS/resolve/main/data/auxiliary/example_piper_2k_spectra.mgf',
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EXAMPLE_PATH / 'example_piper_2k_spectra.mgf',
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"PiperNET example spectra"),
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-
('https://raw.githubusercontent.com/pluskal-lab/DreaMS/
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EXAMPLE_PATH / 'example_5_spectra.mgf',
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"DreaMS example spectra")
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]
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@@ -337,7 +337,9 @@ def _create_result_row(i, j, n, msdata, msdata_lib, sims, cos_sim, embs, calcula
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# Base row data
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row_data = {
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-
'
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'precursor_mz': msdata.get_prec_mzs(i),
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'topk': n + 1,
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'library_j': j,
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@@ -377,10 +379,6 @@ def _process_results_dataframe(df, in_pth, calculate_modified_cosine=False):
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Returns:
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tuple: (processed_df, csv_path)
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"""
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-
# Sort hits by DreaMS similarity
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-
df_top1 = df[df['topk'] == 1].sort_values('DreaMS_similarity', ascending=False)
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-
df = df.set_index('feature_id').loc[df_top1['feature_id'].values].reset_index()
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-
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# Remove unnecessary columns and round similarity scores
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df = df.drop(columns=['i', 'j', 'library_j'])
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df['DreaMS_similarity'] = df['DreaMS_similarity'].astype(float).round(4)
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@@ -390,12 +388,16 @@ def _process_results_dataframe(df, in_pth, calculate_modified_cosine=False):
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df['Modified_cosine_similarity'] = df['Modified_cosine_similarity'].astype(float).round(4)
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df['precursor_mz'] = df['precursor_mz'].astype(float).round(4)
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# Rename columns for display
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column_mapping = {
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'topk': 'Top k',
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'library_ID': 'Library ID',
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-
"
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"precursor_mz": "Precursor m/z",
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"library_SMILES": "Molecule",
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"library_SMILES_raw": "SMILES",
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@@ -625,11 +627,11 @@ def _create_gradio_interface():
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# Results table
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df = gr.Dataframe(
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-
headers=["Row", "
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-
"
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-
datatype=["number", "number", "number", "
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-
col_count=(
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-
column_widths=["
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max_height=1000,
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show_fullscreen_button=True,
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show_row_numbers=False,
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@@ -643,15 +645,15 @@ def _create_gradio_interface():
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# Function to update dataframe headers based on setting
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def update_headers(show_cosine):
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if show_cosine:
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-
return gr.update(headers=["Row", "
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-
"
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-
col_count=(
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-
column_widths=["
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else:
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-
return gr.update(headers=["Row", "
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-
"
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-
col_count=(
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-
column_widths=["
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# Update headers when setting changes
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calculate_modified_cosine.change(
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('https://huggingface.co/datasets/roman-bushuiev/GeMS/resolve/main/data/auxiliary/example_piper_2k_spectra.mgf',
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EXAMPLE_PATH / 'example_piper_2k_spectra.mgf',
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"PiperNET example spectra"),
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+
('https://raw.githubusercontent.com/pluskal-lab/DreaMS/refs/heads/main/data/examples/example_5_spectra.mgf',
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EXAMPLE_PATH / 'example_5_spectra.mgf',
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"DreaMS example spectra")
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]
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# Base row data
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row_data = {
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+
'scan_number': msdata.get_values(SCAN_NUMBER, i),
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+
'rt': msdata.get_values(RT, i),
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+
'charge': msdata.get_values(CHARGE, i),
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'precursor_mz': msdata.get_prec_mzs(i),
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'topk': n + 1,
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'library_j': j,
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Returns:
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tuple: (processed_df, csv_path)
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"""
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# Remove unnecessary columns and round similarity scores
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df = df.drop(columns=['i', 'j', 'library_j'])
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df['DreaMS_similarity'] = df['DreaMS_similarity'].astype(float).round(4)
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df['Modified_cosine_similarity'] = df['Modified_cosine_similarity'].astype(float).round(4)
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df['precursor_mz'] = df['precursor_mz'].astype(float).round(4)
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+
df['rt'] = df['rt'].astype(float).round(2) # Round retention time to 2 decimal places
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+
df['charge'] = df['charge'].astype(str) # Keep charge as string
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# Rename columns for display
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column_mapping = {
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'topk': 'Top k',
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'library_ID': 'Library ID',
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+
"scan_number": "Scan number",
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+
"rt": "Retention time",
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+
"charge": "Charge",
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"precursor_mz": "Precursor m/z",
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"library_SMILES": "Molecule",
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"library_SMILES_raw": "SMILES",
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# Results table
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df = gr.Dataframe(
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+
headers=["Row", "Scan number", "Retention time", "Charge", "Precursor m/z", "Molecule", "Spectrum",
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+
"DreaMS similarity", "Library ID"],
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+
datatype=["number", "number", "number", "str", "number", "html", "html", "number", "str"],
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+
col_count=(9, "fixed"),
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+
column_widths=["20px", "30px", "30px", "25px", "30px", "40px", "40px", "40px", "50px"],
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max_height=1000,
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show_fullscreen_button=True,
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show_row_numbers=False,
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# Function to update dataframe headers based on setting
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def update_headers(show_cosine):
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if show_cosine:
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+
return gr.update(headers=["Row", "Scan number", "Retention time", "Charge", "Precursor m/z", "Molecule", "Spectrum",
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+
"DreaMS similarity", "Library ID", "Modified cosine similarity"],
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+
col_count=(10, "fixed"),
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+
column_widths=["20px", "30px", "30px", "25px", "30px", "40px", "40px", "40px", "50px", "40px"])
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else:
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+
return gr.update(headers=["Row", "Scan number", "Retention time", "Charge", "Precursor m/z", "Molecule", "Spectrum",
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+
"DreaMS similarity", "Library ID"],
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+
col_count=(9, "fixed"),
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+
column_widths=["20px", "30px", "30px", "25px", "30px", "40px", "40px", "40px", "50px"])
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# Update headers when setting changes
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calculate_modified_cosine.change(
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data/example_5_spectra.mgf
DELETED
@@ -1,350 +0,0 @@
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1 |
-
BEGIN IONS
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2 |
-
NAME=DMAPT
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3 |
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DESCRIPTION=MCE bioactive compounds library
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4 |
-
EXACTMASS=293.199094
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5 |
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FORMULA=C17H27NO3
|
6 |
-
INCHI=InChI=1S/C17H27NO3/c1-11-6-5-9-17(2)15(21-17)14-12(8-7-11)13(10-18(3)4)16(19)20-14/h6,12-15H,5,7-10H2,1-4H3/b11-6-/t12-,13+,14-,15+,17+/m0/s1
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7 |
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INCHIAUX=UJNSFDHVIBGEJZ-CMRIBGNTSA-N
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SMILES=C/C1=C/CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)[C@H](CN(C)C)[C@@H]2CC1
|
9 |
-
FEATURE_ID=-1
|
10 |
-
MSLEVEL=2
|
11 |
-
RTINSECONDS=69.34
|
12 |
-
ADDUCT=[M+H]+
|
13 |
-
PEPMASS=294.20637
|
14 |
-
CHARGE=1
|
15 |
-
SPECTYPE=ALL_ENERGIES
|
16 |
-
Collision energy=60.0
|
17 |
-
FRAGMENTATION_METHOD=HCD
|
18 |
-
ISOLATION_WINDOW=1.2000000476839432
|
19 |
-
Acquisition=Crude
|
20 |
-
INSTRUMENT_TYPE=Orbitrap
|
21 |
-
SOURCE_INSTRUMENT=Orbitrap ID-X
|
22 |
-
IMS_TYPE=none
|
23 |
-
ION_SOURCE=ESI
|
24 |
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IONMODE=Positive
|
25 |
-
PI=Tomas Pluskal
|
26 |
-
DATACOLLECTOR=Corinna Brungs
|
27 |
-
DATASET_ID=MSVPLACEHOLDERID
|
28 |
-
USI=mzspec:MSVPLACEHOLDERID:20220601_100AGC_pluskal_mce_1D1_A13_id.mzML:-1
|
29 |
-
SCANS=-1
|
30 |
-
PRECURSOR_PURITY=1.0
|
31 |
-
QUALITY_CHIMERIC=PASSED
|
32 |
-
QUALITY_EXPLAINED_INTENSITY=0.95719075
|
33 |
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QUALITY_EXPLAINED_SIGNALS=0.91803277
|
34 |
-
Num peaks=61
|
35 |
-
42.033739 2.023
|
36 |
-
43.017743 1.244
|
37 |
-
43.041538 0.375
|
38 |
-
44.049385 0.271
|
39 |
-
46.064932 0.633
|
40 |
-
55.053921 0.247
|
41 |
-
56.049297 0.434
|
42 |
-
58.061086 0.921
|
43 |
-
58.064829 100
|
44 |
-
58.068315 4.309
|
45 |
-
58.071661 1.067
|
46 |
-
58.074808 0.3
|
47 |
-
67.053963 0.832
|
48 |
-
69.069565 0.262
|
49 |
-
79.053978 1.014
|
50 |
-
81.069616 1.317
|
51 |
-
82.064804 0.901
|
52 |
-
84.080497 0.567
|
53 |
-
91.053903 1.516
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54 |
-
93.069577 2.084
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55 |
-
94.064888 0.298
|
56 |
-
95.048843 0.28
|
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-
95.085147 0.577
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58 |
-
97.088348 0.201
|
59 |
-
98.059745 0.372
|
60 |
-
105.069597 1.626
|
61 |
-
106.064804 0.358
|
62 |
-
107.085253 1.159
|
63 |
-
108.080338 0.242
|
64 |
-
109.064416 0.257
|
65 |
-
109.100923 0.465
|
66 |
-
110.096075 1.043
|
67 |
-
116.070213 0.429
|
68 |
-
117.069763 0.601
|
69 |
-
119.085279 1.489
|
70 |
-
121.100884 0.483
|
71 |
-
129.069626 0.285
|
72 |
-
131.085311 0.665
|
73 |
-
133.10089 0.474
|
74 |
-
134.059753 0.937
|
75 |
-
135.117294 0.205
|
76 |
-
144.093231 0.522
|
77 |
-
145.100601 0.202
|
78 |
-
147.11673 0.298
|
79 |
-
149.13218 2.214
|
80 |
-
159.116485 2.567
|
81 |
-
161.131911 0.35
|
82 |
-
164.107071 0.243
|
83 |
-
164.143127 0.255
|
84 |
-
175.112091 0.209
|
85 |
-
177.127193 1.388
|
86 |
-
185.13264 0.432
|
87 |
-
192.174698 0.38
|
88 |
-
203.14307 0.317
|
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-
222.185104 0.206
|
90 |
-
231.13818 0.57
|
91 |
-
249.148476 2.331
|
92 |
-
250.216614 0.841
|
93 |
-
251.117976 1.62
|
94 |
-
294.128296 0.191
|
95 |
-
294.206632 26.983
|
96 |
-
END IONS
|
97 |
-
|
98 |
-
BEGIN IONS
|
99 |
-
NAME=Mirk-IN-1
|
100 |
-
DESCRIPTION=MCE bioactive compounds library
|
101 |
-
EXACTMASS=497.065759
|
102 |
-
FORMULA=C23H17Cl2N5O4
|
103 |
-
INCHI=InChI=1S/C23H17Cl2N5O4/c1-34-23-27-11-14-8-16(22(33)29-19(14)30-23)21(32)28-18-9-13(5-6-17(18)25)20(31)26-10-12-3-2-4-15(24)7-12/h2-9,11H,10H2,1H3,(H,26,31)(H,28,32)(H,27,29,30,33)
|
104 |
-
INCHIAUX=CQKBSRPVZZLCJE-UHFFFAOYSA-N
|
105 |
-
SMILES=COc1ncc2cc(C(=O)Nc3c(Cl)ccc(C(=O)NCc4cc(Cl)ccc4)c3)c(=O)[nH]c2n1
|
106 |
-
FEATURE_ID=-1
|
107 |
-
MSLEVEL=2
|
108 |
-
RTINSECONDS=115.08
|
109 |
-
ADDUCT=[M+H]+
|
110 |
-
PEPMASS=498.07304
|
111 |
-
CHARGE=1
|
112 |
-
SPECTYPE=ALL_MSN_TO_PSEUDO_MS2
|
113 |
-
Collision energy=60.0
|
114 |
-
FRAGMENTATION_METHOD=HCD
|
115 |
-
ISOLATION_WINDOW=1.2000000476839432
|
116 |
-
Acquisition=Crude
|
117 |
-
INSTRUMENT_TYPE=Orbitrap
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118 |
-
SOURCE_INSTRUMENT=Orbitrap ID-X
|
119 |
-
IMS_TYPE=none
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120 |
-
ION_SOURCE=ESI
|
121 |
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IONMODE=Positive
|
122 |
-
PI=Tomas Pluskal
|
123 |
-
DATACOLLECTOR=Corinna Brungs
|
124 |
-
DATASET_ID=MSVPLACEHOLDERID
|
125 |
-
USI=mzspec:MSVPLACEHOLDERID:20220601_pluskal_mce_1D1_A4_id.mzML:-1
|
126 |
-
SCANS=-1
|
127 |
-
PRECURSOR_PURITY=1.0
|
128 |
-
QUALITY_CHIMERIC=PASSED
|
129 |
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QUALITY_EXPLAINED_INTENSITY=0.93082154
|
130 |
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QUALITY_EXPLAINED_SIGNALS=0.88461536
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-
Num peaks=52
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132 |
-
42.033703 6.933
|
133 |
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58.028778 11.37
|
134 |
-
59.032055 2.116
|
135 |
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63.022655 2.006
|
137 |
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|
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65.038353 0.923
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139 |
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|
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69.992175 1.938
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141 |
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79.028745 1.257
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143 |
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86.060081 9.959
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144 |
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87.06353 3.769
|
145 |
-
88.064438 1.499
|
146 |
-
91.017532 3.789
|
147 |
-
93.044386 7.213
|
148 |
-
104.049591 5.292
|
149 |
-
105.044537 4.776
|
150 |
-
105.052979 3.494
|
151 |
-
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|
152 |
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120.055412 7.778
|
153 |
-
121.039436 6.751
|
154 |
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125.014962 2.948
|
155 |
-
133.027011 2.074
|
156 |
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133.039425 3.979
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157 |
-
135.018616 0.908
|
158 |
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148.050389 4.721
|
159 |
-
154.005085 2.139
|
160 |
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160.050642 3.311
|
161 |
-
161.034588 1.467
|
162 |
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176.045663 22.882
|
163 |
-
194.056314 24.336
|
164 |
-
204.040476 24.707
|
165 |
-
221.080734 1.76
|
166 |
-
222.05116 100
|
167 |
-
222.087845 1.473
|
168 |
-
223.089127 1.679
|
169 |
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248.069031 1.01
|
170 |
-
249.074326 2.424
|
171 |
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|
172 |
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251.081848 1.513
|
173 |
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277.029205 1.552
|
174 |
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293.066956 1.309
|
175 |
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|
176 |
-
309.15033 3.711
|
177 |
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|
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321.062225 1.269
|
179 |
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357.03932 4.785
|
180 |
-
411.191315 1.423
|
181 |
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|
182 |
-
413.196318 8.005
|
183 |
-
498.073273 1.812
|
184 |
-
END IONS
|
185 |
-
|
186 |
-
BEGIN IONS
|
187 |
-
NAME=1373215-15-6
|
188 |
-
DESCRIPTION=MCE bioactive compounds library
|
189 |
-
EXACTMASS=484.212198
|
190 |
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FORMULA=C25H29FN4O5
|
191 |
-
INCHI=InChI=1S/C25H29FN4O5/c1-27-25(32)35-22-15-34-21-7-6-18(29-8-10-30(11-9-29)19-13-33-14-19)12-20(21)23(22)28-24(31)16-2-4-17(26)5-3-16/h2-7,12,19,22-23H,8-11,13-15H2,1H3,(H,27,32)(H,28,31)/t22-,23-/m0/s1
|
192 |
-
INCHIAUX=NDEBZCZEAVMSQF-GOTSBHOMSA-N
|
193 |
-
SMILES=CNC(=O)O[C@H]1COc2c(cc(N3CCN(C4COC4)CC3)cc2)[C@@H]1NC(=O)c1ccc(F)cc1
|
194 |
-
FEATURE_ID=-1
|
195 |
-
MSLEVEL=2
|
196 |
-
RTINSECONDS=77.81
|
197 |
-
ADDUCT=[M+H]+
|
198 |
-
PEPMASS=485.21947
|
199 |
-
CHARGE=1
|
200 |
-
SPECTYPE=SAME_ENERGY
|
201 |
-
Collision energy=30.0
|
202 |
-
FRAGMENTATION_METHOD=HCD
|
203 |
-
ISOLATION_WINDOW=1.2000000476839432
|
204 |
-
Acquisition=Crude
|
205 |
-
INSTRUMENT_TYPE=Orbitrap
|
206 |
-
SOURCE_INSTRUMENT=Orbitrap ID-X
|
207 |
-
IMS_TYPE=none
|
208 |
-
ION_SOURCE=ESI
|
209 |
-
IONMODE=Positive
|
210 |
-
PI=Tomas Pluskal
|
211 |
-
DATACOLLECTOR=Corinna Brungs
|
212 |
-
DATASET_ID=MSVPLACEHOLDERID
|
213 |
-
USI=mzspec:MSVPLACEHOLDERID:20220601_pluskal_mce_1D1_A8_id.mzML:-1
|
214 |
-
SCANS=-1
|
215 |
-
PRECURSOR_PURITY=1.0
|
216 |
-
QUALITY_CHIMERIC=PASSED
|
217 |
-
QUALITY_EXPLAINED_INTENSITY=1.0
|
218 |
-
QUALITY_EXPLAINED_SIGNALS=1.0
|
219 |
-
Num peaks=15
|
220 |
-
70.064962 2.862
|
221 |
-
84.080627 1.511
|
222 |
-
109.076332 1.385
|
223 |
-
114.091324 2.886
|
224 |
-
123.023911 14.149
|
225 |
-
161.059692 2.52
|
226 |
-
202.086288 1.435
|
227 |
-
230.105148 3.367
|
228 |
-
241.133691 26.664
|
229 |
-
261.159847 3.062
|
230 |
-
271.144251 41.501
|
231 |
-
289.154956 100
|
232 |
-
346.175893 26.1
|
233 |
-
351.136749 1.2
|
234 |
-
410.186693 8.75
|
235 |
-
END IONS
|
236 |
-
|
237 |
-
BEGIN IONS
|
238 |
-
NAME=IPSU
|
239 |
-
DESCRIPTION=MCE bioactive compounds library
|
240 |
-
EXACTMASS=405.216475
|
241 |
-
FORMULA=C23H27N5O2
|
242 |
-
INCHI=InChI=1S/C23H27N5O2/c1-30-20-7-11-24-22(26-20)27-13-9-23(10-14-27)8-4-12-28(21(23)29)16-17-15-25-19-6-3-2-5-18(17)19/h2-3,5-7,11,15,25H,4,8-10,12-14,16H2,1H3
|
243 |
-
INCHIAUX=PCMHOSYCWRRHTG-UHFFFAOYSA-N
|
244 |
-
SMILES=COc1nc(N2CCC3(CCCN(Cc4c[nH]c5ccccc45)C3=O)CC2)ncc1
|
245 |
-
FEATURE_ID=660
|
246 |
-
MSLEVEL=2
|
247 |
-
RTINSECONDS=110.45
|
248 |
-
ADDUCT=[M+H]+
|
249 |
-
PEPMASS=406.22375
|
250 |
-
CHARGE=1
|
251 |
-
Collision energy=20.0
|
252 |
-
FRAGMENTATION_METHOD=HCD
|
253 |
-
ISOLATION_WINDOW=1.2000000476839432
|
254 |
-
Acquisition=Crude
|
255 |
-
INSTRUMENT_TYPE=Orbitrap
|
256 |
-
SOURCE_INSTRUMENT=Orbitrap ID-X
|
257 |
-
IMS_TYPE=none
|
258 |
-
ION_SOURCE=ESI
|
259 |
-
IONMODE=Positive
|
260 |
-
PI=Tomas Pluskal
|
261 |
-
DATACOLLECTOR=Corinna Brungs
|
262 |
-
DATASET_ID=MSVPLACEHOLDERID
|
263 |
-
USI=mzspec:MSVPLACEHOLDERID:20220601_pluskal_mce_1D1_A1_id.mzML:660
|
264 |
-
SCANS=660
|
265 |
-
PRECURSOR_PURITY=0.9731724062527856
|
266 |
-
QUALITY_CHIMERIC=PASSED
|
267 |
-
QUALITY_EXPLAINED_INTENSITY=0.99532574
|
268 |
-
QUALITY_EXPLAINED_SIGNALS=0.8888889
|
269 |
-
Num peaks=9
|
270 |
-
45.134823 1.082
|
271 |
-
45.13699 1.064
|
272 |
-
110.096245 17.184
|
273 |
-
130.064972 13.97
|
274 |
-
136.111862 0.874
|
275 |
-
277.16571 100
|
276 |
-
289.165924 52.842
|
277 |
-
307.177856 0.793
|
278 |
-
406.223083 43.696
|
279 |
-
END IONS
|
280 |
-
|
281 |
-
BEGIN IONS
|
282 |
-
NAME=Vadimezan
|
283 |
-
DESCRIPTION=MCE bioactive compounds library
|
284 |
-
EXACTMASS=282.089209
|
285 |
-
FORMULA=C17H14O4
|
286 |
-
INCHI=InChI=1S/C17H14O4/c1-9-6-7-13-15(20)12-5-3-4-11(8-14(18)19)17(12)21-16(13)10(9)2/h3-7H,8H2,1-2H3,(H,18,19)
|
287 |
-
INCHIAUX=XGOYIMQSIKSOBS-UHFFFAOYSA-N
|
288 |
-
SMILES=Cc1c(C)c2c(cc1)c(=O)c1cccc(CC(=O)O)c1o2
|
289 |
-
FEATURE_ID=474
|
290 |
-
MSLEVEL=2
|
291 |
-
RTINSECONDS=113.94
|
292 |
-
ADDUCT=[M+H]+
|
293 |
-
PEPMASS=283.09648
|
294 |
-
CHARGE=1
|
295 |
-
Collision energy=60.0
|
296 |
-
FRAGMENTATION_METHOD=HCD
|
297 |
-
ISOLATION_WINDOW=1.2000000476839432
|
298 |
-
Acquisition=Crude
|
299 |
-
INSTRUMENT_TYPE=Orbitrap
|
300 |
-
SOURCE_INSTRUMENT=Orbitrap ID-X
|
301 |
-
IMS_TYPE=none
|
302 |
-
ION_SOURCE=ESI
|
303 |
-
IONMODE=Positive
|
304 |
-
PI=Tomas Pluskal
|
305 |
-
DATACOLLECTOR=Corinna Brungs
|
306 |
-
DATASET_ID=MSVPLACEHOLDERID
|
307 |
-
USI=mzspec:MSVPLACEHOLDERID:20220601_pluskal_mce_1D1_A2_id.mzML:474
|
308 |
-
SCANS=474
|
309 |
-
PRECURSOR_PURITY=0.973405752811273
|
310 |
-
QUALITY_CHIMERIC=PASSED
|
311 |
-
QUALITY_EXPLAINED_INTENSITY=0.99386805
|
312 |
-
QUALITY_EXPLAINED_SIGNALS=0.9444444
|
313 |
-
Num peaks=36
|
314 |
-
91.053741 1.144
|
315 |
-
105.069382 1.254
|
316 |
-
141.069168 1.139
|
317 |
-
152.061859 1.019
|
318 |
-
153.069305 1.283
|
319 |
-
155.085022 0.966
|
320 |
-
158.033508 1.081
|
321 |
-
165.069733 7.345
|
322 |
-
166.077545 9.805
|
323 |
-
167.085587 4.037
|
324 |
-
168.093094 3.638
|
325 |
-
178.077515 2.42
|
326 |
-
179.085281 1.429
|
327 |
-
181.06459 6.555
|
328 |
-
181.101135 2.534
|
329 |
-
183.116669 0.903
|
330 |
-
190.078049 0.997
|
331 |
-
191.085159 1.264
|
332 |
-
193.101242 1.467
|
333 |
-
194.07254 10.324
|
334 |
-
195.080231 21.628
|
335 |
-
196.087906 3.722
|
336 |
-
208.088181 2.735
|
337 |
-
209.059555 0.982
|
338 |
-
209.096024 59.124
|
339 |
-
209.119858 0.749
|
340 |
-
210.104065 2.296
|
341 |
-
221.096359 0.981
|
342 |
-
222.067566 2.431
|
343 |
-
223.0755 19.616
|
344 |
-
225.091003 2.035
|
345 |
-
236.083176 2.085
|
346 |
-
237.090988 100
|
347 |
-
238.098816 15.987
|
348 |
-
239.106781 0.935
|
349 |
-
283.096832 2.447
|
350 |
-
END IONS
|
|
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