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Open AccessJournal ArticleDOI

A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.

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TLDR
The expanded CMap is reported, made possible by a new, low-cost, high-throughput reduced representation expression profiling method that is shown to be highly reproducible, comparable to RNA sequencing, and suitable for computational inference of the expression levels of 81% of non-measured transcripts.
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This article is published in Cell.The article was published on 2017-11-30 and is currently open access. It has received 1943 citations till now.

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Morphological Subprofile Analysis for Bioactivity Annotation of Small Molecules

TL;DR: In this article , the authors introduce the concept of subprofile analysis to map the mode of action for both reference and unexplored compounds, and extract subprofiles that contain only a subset of morphological features to represent a consensus profile.
Journal ArticleDOI

Power analysis for RNA-Seq differential expression studies using generalized linear mixed effects models.

TL;DR: A novel simulation based procedure for power estimation of differential expression with the employment of generalized linear mixed effects models for correlated expression data is proposed and properly control the false positive rate at the nominal level.
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MARSY: A multitask deep learning framework for prediction of drug combination synergy scores

TL;DR: MARSY is a deep learning multi-task model that incorporates information on gene expression profile of cancer cell lines, as well as the differential expression signature induced by each drug to predict drug-pair synergy scores, confirming the ability of MARSY in making accurate novel predictions.
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Cell-specific imputation of drug connectivity mapping with incomplete data

TL;DR: Slonim et al. as discussed by the authors compared collaborative filtering with either neighborhood-based or SVD imputation methods to two naive approaches via cross-validation, and concluded that even for cells in which drug responses have not been fully characterized, it is possible to identify unassayed drugs that reverse in those cells the expression signatures observed in disease.
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Metabolomics paves the way for improved drug target identification

TL;DR: Proof‐of‐concept for a new way to identify drug–target interactions using high‐throughput metabolomics is demonstrated, potentially paving the way towards a universal method for predicting drug– target relationships.
References
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Journal Article

Visualizing Data using t-SNE

TL;DR: A new technique called t-SNE that visualizes high-dimensional data by giving each datapoint a location in a two or three-dimensional map, a variation of Stochastic Neighbor Embedding that is much easier to optimize, and produces significantly better visualizations by reducing the tendency to crowd points together in the center of the map.
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Gene Expression Omnibus: NCBI gene expression and hybridization array data repository

TL;DR: The Gene Expression Omnibus (GEO) project was initiated in response to the growing demand for a public repository for high-throughput gene expression data and provides a flexible and open design that facilitates submission, storage and retrieval of heterogeneous data sets from high-power gene expression and genomic hybridization experiments.
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BLAT—The BLAST-Like Alignment Tool

TL;DR: How BLAT was optimized is described, which is more accurate and 500 times faster than popular existing tools for mRNA/DNA alignments and 50 times faster for protein alignments at sensitivity settings typically used when comparing vertebrate sequences.
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Adjusting batch effects in microarray expression data using empirical Bayes methods

TL;DR: This paper proposed parametric and non-parametric empirical Bayes frameworks for adjusting data for batch effects that is robust to outliers in small sample sizes and performs comparable to existing methods for large samples.
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