Proteomics and Biomarker Discovery

This dataset provides comprehensive protein expression profiles, mass spectrometry results, post-translational modification details, and protein-protein interaction data, enabling robust biomarker discovery for disease research. It is designed for integrative analysis in proteomics, supporting both experimental and computational approaches to uncover disease mechanisms and candidate biomarkers.

  • last updated 2 Nov 2025
  • by GoMask
The brief that made it

Identification of candidate biomarkers for disease diagnosis and prognosis

Sample rows

preview · 8 of 105 rows · all 17 columns
protein_idstringdisease_statusstringprotein_abundancefloatbiomarker_candidatebooleanpost_translational_modification_typestringprotein_namestringgene_symbolstringorganismstringsample_idstringmass_spectrometry_methodstringabundance_unitstringmodification_sitestringinteraction_partner_idstringinteraction_typestringbiomarker_evidence_levelstringexperiment_datedatedata_sourcestring
P00001healthy18452.65falsephosphorylationSerum albuminALBHomo sapiensSAMP001LC-MS/MSiBAQS34P00007complexblank2021-07-15PRIDE
P00002disease321421.84trueglycosylationAlpha-1-antitrypsinSERPINA1Homo sapiensSAMP002MALDI-TOFspectral countN413P00010directexperimental2022-02-23published study
Q9Y6R7control1853.46falseblankVimentinVIMHomo sapiensSAMP003SWATH-MSFPKMblankblankblankblank2020-09-04PRIDE
P00004unknown239.97falseacetylationTransferrinTFHomo sapiensSAMP004CE-MSFPKMK18blankblankblank2020-02-13in-house
Q13509disease69437.4truephosphorylationC-reactive proteinCRPHomo sapiensSAMP005LC-MS/MSspectral countT87P00001complexliterature2022-06-21in-house
P00006healthy3561.12falseblankTubulin beta chainTUBBHomo sapiensSAMP006SWATH-MSiBAQblankblankblankblank2021-03-10PRIDE
P00007control12489.75truemethylationHeat shock protein HSP 90HSP90Homo sapiensSAMP007LC-MS/MSiBAQR51P00015transientexperimental2023-04-09published study
P00008disease254622.2falseubiquitinationMyosin heavy chain 9MYH9Homo sapiensSAMP008MALDI-TOFspectral countK120P00010complexblank2022-12-12published study

What the 105 rows show

from the 105-row sample

Disease (disease status) stands out: 33 of its 41 rows have biomarker_candidate = true, against 6 of 64 for the rest.

  • 37%biomarker_candidate = true
  • 8,827median protein_abundance
  • 3abundance units
  • 3data sources
  • 4mass spectrometry methods
  • 4interaction types
Biomarker candidate rate by disease_statusbiomarker_candidate = true
0%50%100%0%healthy0 of 2280%disease33 of 415%control1 of 2124%unknown5 of 21

Disease (disease status)'s mean protein_abundance is 119,746, against 6,292 for healthy, 4,042 for control and 2,744 for unknown.

protein_abundance105 rows, in bands of 100k
04590906521000010500k1Mprotein_abundance →

Median 8,827, from 0.03 to 983,441.

post_translational_modification_type70 rows with a value · 35 left blank
  1. phosphorylation26
  2. glycosylation15
  3. acetylation10
  4. methylation8
  5. ubiquitination5
  6. oxidation3
  7. hydroxylation2
  8. unknown1
17 columns by typefrom the column list below
  • string 14
  • float 1
  • date 1
  • boolean 1

Columns

17 columns in four groups
blueprint · 17 columns
columntypedescriptionexample
Text 14 columns
protein_idstringUnique identifier for the protein (e.g., UniProt accession number)uniqueP00001
protein_namestringStandardized name of the proteinSerum albumin
gene_symbolstringGene symbol associated with the proteinoptionalALB
organismstringOrganism from which the protein sample was derived7 organismsHomo sapiens
sample_idstringIdentifier for the biological sample analyzedSAMP001
disease_statusstringDisease status of the sample (e.g., healthy, disease, control)healthy · disease · control · unknown · optionalhealthy
mass_spectrometry_methodstringType of mass spectrometry used (e.g., LC-MS/MS, MALDI-TOF)4 methods · optionalLC-MS/MS
abundance_unitstringUnit of measurement for protein abundance (e.g., FPKM, iBAQ, spectral count)3 units · optionaliBAQ
post_translational_modification_typestringType of post-translational modification detected (e.g., phosphorylation, glycosylation)8 types · optionalphosphorylation
modification_sitestringAmino acid residue and position of modification (e.g., S15 for serine at position 15)optionalS34
interaction_partner_idstringIdentifier for the protein interaction partner (e.g., UniProt accession number)optionalP00007
interaction_typestringType of protein-protein interaction (e.g., direct, complex, transient)direct · complex · transient · unknown · optionalcomplex
biomarker_evidence_levelstringLevel of evidence supporting biomarker candidacy (e.g., experimental, computational, literature)experimental · computational · literature · unknown · optionalexperimental
data_sourcestringSource or repository of the data (e.g., PRIDE, in-house, published study)3 sources · optionalPRIDE
Numbers 1 column
protein_abundancefloatQuantitative measurement of protein abundance (e.g., intensity, spectral count)0 or more18452.65
Dates and times 1 column
experiment_datedateDate when the mass spectrometry experiment was performedoptional2021-07-15
True or false 1 column
biomarker_candidatebooleanIndicates if the protein is a candidate biomarker for diseasefalse

Use it for

  • biomarker cand…37%39 of 105 rowsmean protein abundanc…6.3kheal…119.7kdise…4kcont…2.7kunkn…

    A healthcare dashboard

    The biomarker_candidate rate, protein_abundance by disease_status and a breakdown of post_translational_modification_type. Excel, Power BI or Tableau.

  • Why do 39 of 105 rows have biomarker_candidate = true?

    A root-cause class exercise

    Hand out the rows and one question. The answer is in the data, not in the brief.

  • A software demo

    Believable proteins with protein_name, gene_symbol and organism to fill a screen in front of a buyer.

Not quite right?

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This dataset105 rows17 columns
Yours1,000 rows17 columnsmodification_site: UK only

blueprint · proteomics-and-biomarker-discovery

Behind this dataset

Same schema. As many rows as you need.

These 105 rows came out of a blueprint — 17 columns with generation rules behind each one. Open it in Data Factory to retune a column, add your own, wire in foreign keys, and run it at the size you actually need.

Rules it was built with
  • Sample ID unique per specimen
  • Sample type: tissue, serum, plasma, urine, CSF
  • Mass spectrometry platform: Orbitrap, Q-TOF, triple quad
  • Quantification method: label-free, TMT, SILAC
  • Protein identification: UniProt ID
  • Peptide sequences and modifications
  • Protein abundance: spectral counts, intensity
  • Post-translational modifications: phosphorylation, acetylation, ubiquitination
Rows
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Exports
CSV, JSON, JSONL, Parquet, SQL, Excel, TSV, XML
Licence
yours to use, including commercially
API slug
proteomics-and-biomarker-discovery

What should your data show?

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