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L1000 LINCS DCIC REP.B028 JURKAT 24H M17 pirfenidone 0.03uM.tsv.gz (File)

Subject:

JURKAT

Subject (Entity type)
Project:

LINCS-2021

Project (Entity type)
Ncbi Taxonomy:

Homo sapiens

Taxonomy (Entity type)
File Format:

TSV

File Format (Entity type)
Disease:

leukemia

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.B028 JURKAT 24H M17 pirfenidone 0.03uM

Biosample (Entity type)
Assay Type:

landmark transcript profiling assay

Assay Type (Entity type)
Anatomy:

Blood

Anatomy (Entity type)
Uncompressed Size In Bytes:180 KB
Size In Bytes:84.6 KB
Sha256:32f82e5bf981ab3c63caaab585485689d36be9bf30206ef5c71ebd5790480cc1
Mime Type:application/gzip
Md5:fad074e22a3fff1c81d22c01de417926
Filename:L1000_LINCS_DCIC_REP.B028_JURKAT_24H_M17_pirfenidone_0.03uM.tsv.gz
Creation Time:2021-01-21 00:00:00.000000
Access URL:
drs://drs.lincs-dcic.org/fad074e22a3fff1c81d22c01de417926
Workbench DRS:
drs://cfde.cloud/36e0b3b1-c4f7-506d-ac59-ba935c3dc660
Results found

Linked to

 

Label

Description

 

Biosample

L1000 LINCS DCIC 2021 REP.B028 JURKAT 24H M17 pirfenidone 0.03uM

Biosample (Entity type)

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

  • Biosample

    L1000 LINCS DCIC 2021 REP.B028 JURKAT 24H M17 pirfenidone 0.03uM

    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.