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L1000 LINCS DCIC MOAR010 OVTOKO 24H F05 riodipine 3.33uM.tsv.gz (File)

Project:

LINCS-2021

Project (Entity type)
Id Namespace:

Library of Integrated Network-Based Cellular Signatures

Identifier Namespace (Entity type)
File Format:

TSV

File Format (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)
Assay Type:

landmark transcript profiling assay

Assay Type (Entity type)
Uncompressed Size In Bytes:312 KB
Size In Bytes:131 KB
Sha256:14a5140e943e3816f46bfac26005cca4cf3dc43fe7d988dfaa838bc6c7da95b0
Persistent Id:drs://drs.lincs-dcic.org/0a19c60909870bd5373ad37ef347a1be
Mime Type:application/gzip
Md5:0a19c60909870bd5373ad37ef347a1be
Filename:L1000_LINCS_DCIC_MOAR010_OVTOKO_24H_F05_riodipine_3.33uM.tsv.gz
Creation Time:2021-01-21T00:00:00
Access Url:
drs://drs.lincs-dcic.org/0a19c60909870bd5373ad37ef347a1be
Results found

Linked to

 

Label

Description

 

Subject

OVTOKO

Subject (Entity type)

A subject from LINCS produced as part of the LINCS project

Biosample

L1000 LINCS DCIC 2021 MOAR010 OVTOKO 24H F05 riodipine 3.33uM

Biosample (Entity type)

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

  • Subject

    OVTOKO

    Subject (Entity type)

    A subject from LINCS produced as part of the LINCS project

  • Biosample

    L1000 LINCS DCIC 2021 MOAR010 OVTOKO 24H F05 riodipine 3.33uM

    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
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    Data & MetadataToolsChatbotUse CasesPublications
    CFDE Workbench
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    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.