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L1000 LINCS DCIC REP.A013 PC3 24H L11 cyclobenzaprine 0.125uM.tsv.gz (File)

Subject:

PC3

Subject (Entity type)
Project:

LINCS-2021

Project (Entity type)
Ncbi Taxonomy:

Homo sapiens

Taxonomy (Entity type)
File Format:

TSV

File Format (Entity type)
Disease:

prostate adenocarcinoma

Disease (Entity type)
Dcc Asset:

datapackage.zip

Processed File (Entity type)
Dcc:

LINCS

DCC (Entity type)
Data Type:

Gene expression profile

Data Type (Entity type)
Compression Format:

GZIP format

File Format (Entity type)
Biosample:

L1000 LINCS DCIC 2021 REP.A013 PC3 24H L11 cyclobenzaprine 0.125uM

Biosample (Entity type)
Assay Type:

landmark transcript profiling assay

Assay Type (Entity type)
Anatomy:

prostate gland

Anatomy (Entity type)
Uncompressed Size In Bytes:270 KB
Size In Bytes:127 KB
Sha256:d8947fbd3162e4b20cdb738db68188b128f65a75ef1efe2adad568d9bc7ed672
Mime Type:application/gzip
Md5:13e44110bdd31c29b1ead4bed3733b9a
Filename:L1000_LINCS_DCIC_REP.A013_PC3_24H_L11_cyclobenzaprine_0.125uM.tsv.gz
Creation Time:2021-01-21 00:00:00.000000
Access URL:
drs://drs.lincs-dcic.org/13e44110bdd31c29b1ead4bed3733b9a
Workbench DRS:
drs://cfde.cloud/a17f9a3a-bd6b-5d7f-93a5-ed873e3d9f50
Results found

Linked to

 

Label

Description

 

Biosample

L1000 LINCS DCIC 2021 REP.A013 PC3 24H L11 cyclobenzaprine 0.125uM

Biosample (Entity type)

A biosample from LINCS produced as part of the LINCS 2021 project

  • Biosample

    L1000 LINCS DCIC 2021 REP.A013 PC3 24H L11 cyclobenzaprine 0.125uM

    Biosample (Entity type)

    A biosample from LINCS produced as part of the LINCS 2021 project

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    Workbench TutorialTraining & OutreachDocumentationGet QR CodesFunding Opportunities
    Resources
    Data & MetadataToolsChatbotUse CasesPublications
    CFDE Workbench
    Report a bug
    The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.
    @CFDE Workbench 2026
    This repository is under review for potential modification in compliance with Administration directives.