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L1000 LINCS DCIC REP.A009 MDAMB231 24H N22 fenticonazole 0.37uM.tsv.gz (File)

Subject:

MDAMB231

Subject (Entity type)
Project:

LINCS-2021

Project (Entity type)
Ncbi Taxonomy:

Homo sapiens

Taxonomy (Entity type)
File Format:

TSV

File Format (Entity type)
Disease:

breast carcinoma

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.A009 MDAMB231 24H N22 fenticonazole 0.37uM

Biosample (Entity type)
Assay Type:

landmark transcript profiling assay

Assay Type (Entity type)
Anatomy:

Breast

Anatomy (Entity type)
Uncompressed Size In Bytes:363 KB
Size In Bytes:167 KB
Sha256:93ba90341e2890c3e78d1244711c2075c683906d262eaa1edc48b563b245e495
Mime Type:application/gzip
Md5:097730718d13502025b2c75e679af651
Filename:L1000_LINCS_DCIC_REP.A009_MDAMB231_24H_N22_fenticonazole_0.37uM.tsv.gz
Creation Time:2021-01-21 00:00:00.000000
Access URL:
drs://drs.lincs-dcic.org/097730718d13502025b2c75e679af651
Workbench DRS:
drs://cfde.cloud/a110e3ae-cebb-57f2-aae8-4414da9386c8
Results found

Linked to

 

Label

Description

 

Biosample

L1000 LINCS DCIC 2021 REP.A009 MDAMB231 24H N22 fenticonazole 0.37uM

Biosample (Entity type)

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

  • Biosample

    L1000 LINCS DCIC 2021 REP.A009 MDAMB231 24H N22 fenticonazole 0.37uM

    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.