Evidence map›Paper›PMID 25609570›Full record

ArticleMolecular bioSystems2015

Compound signature detection on LINCS L1000 big data.

Chenglin Liu, Jing Su, Fei Yang, Kun Wei, Jinwen Ma, Xiaobo Zhou

Abstract read
In one paragraph

Article in Molecular bioSystems, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chenglin LiuSchool of Mathematical Sciences and LMAM, Peking University, Beijing 100871, China.
Jing Su
Fei Yang
Kun Wei
Jinwen Ma
Xiaobo Zhou

Funding

Modelling the Growth of the MIC Niche at the System LevelU01CA166886 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ZHOU, XIAOBO · 2012 to 2016
$2.2M
itNETZ: Integrative and Translational Network-based Cellular Signature AnalyzerU01HL111560 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ZHOU, XIAOBO · 2011 to 2013
$1.1M
NCI NIH HHS U01 CA166886NHLBI NIH HHS 1U01HL111560NHLBI NIH HHS U01 HL111560
6 · The paper itself

Abstract

The Library of Integrated Network-based Cellular Signatures (LINCS) L1000 big data provide gene expression profiles induced by over 10 000 compounds, shRNAs, and kinase inhibitors using the L1000 platform. We developed csNMF, a systematic compound signature discovery pipeline covering from raw L1000 data processing to drug screening and mechanism generation. The csNMF pipeline demonstrated better performance than the original L1000 pipeline. The discovered compound signatures of breast cancer were consistent with the LINCS KINOMEscan data and were clinically relevant. The csNMF pipeline provided a novel and complete tool to expedite signature-based drug discovery leveraging the LINCS L1000 resources.

Indexed as

Datasets as TopicTranscriptomeBreast NeoplasmsCell Line, TumorComputational BiologyDrug DiscoveryDrug Screening Assays, AntitumorGene Expression ProfilingGene Expression RegulationHumansMolecular Sequence AnnotationProtein Kinase InhibitorsReproducibility of ResultsRNA, Small InterferingSmall Molecule LibrariesWorkflowProtein Kinase InhibitorsRNA, Small InterferingSmall Molecule Libraries

Identifiers

PMID25609570
PMCPMC4333019

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.