# TOPS: a versatile software tool for statistical analysis and visualization of combinatorial gene-gene and gene-drug interaction screens

- Markus K Muellner†
^{1}Email author, - Gerhard Duernberger†
^{1, 2}, - Florian Ganglberger†
^{1}, - Claudia Kerzendorfer
^{1}, - Iris Z Uras
^{1}, - Andreas Schoenegger
^{1}, - Klaudia Bagienski
^{1}, - Jacques Colinge
^{1}and - Sebastian MB Nijman
^{1}Email author

**15**:98

**DOI: **10.1186/1471-2105-15-98

© Muellner et al.; licensee BioMed Central Ltd. 2014

**Received: **17 May 2013

**Accepted: **28 March 2014

**Published: **8 April 2014

## Abstract

### Background

Measuring the impact of combinations of genetic or chemical perturbations on cellular fitness, sometimes referred to as synthetic lethal screening, is a powerful method for obtaining novel insights into gene function and drug action. Especially when performed at large scales, gene-gene or gene-drug interaction screens can reveal complex genetic interactions or drug mechanism of action or even identify novel therapeutics for the treatment of diseases.

The result of such large-scale screen results can be represented as a matrix with a numeric score indicating the cellular fitness (e.g. viability or doubling time) for each double perturbation. In a typical screen, the majority of combinations do not impact the cellular fitness. Thus, it is critical to first discern true "hits" from noise. Subsequent data exploration and visualization methods can assist to extract meaningful biological information from the data. However, despite the increasing interest in combination perturbation screens, no user friendly open-source program exists that combines statistical analysis, data exploration tools and visualization.

### Results

We developed TOPS (Tool for Combination Perturbation Screen Analysis), a Java and R-based software tool with a simple graphical user interface that allows the user to import, analyze, filter and plot data from double perturbation screens as well as other compatible data. TOPS was designed in a modular fashion to allow the user to add alternative importers for data formats or custom analysis scripts not covered by the original release.

We demonstrate the utility of TOPS on two datasets derived from functional genetic screens using different methods. Dataset 1 is a gene-drug interaction screen and is based on Luminex xMAP technology. Dataset 2 is a gene-gene short hairpin (sh)RNAi screen exploring the interactions between deubiquitinating enzymes and a number of prominent oncogenes using massive parallel sequencing (MPS).

### Conclusions

TOPS provides the benchtop scientist with a free toolset to analyze, filter and visualize data from functional genomic gene-gene and gene-drug interaction screens with a flexible interface to accommodate different technologies and analysis algorithms in addition to those already provided here. TOPS is freely available for academic and non-academic users and is released as open source.

### Keywords

Double perturbation screens Synthetic lethality Functional genetics Massive parallel sequencing Luminex xMAP Drug screens Synergy Epistasis## Background

Genes operate in complex cellular networks, and elucidating this connectivity is critical for understanding normal physiology and disease. Functional genomic screens that combine two perturbations have been used with great success to uncover such genetic interactions, and also to reveal mechanisms of drug action [1, 2]. This is generally done by perturbing a biological system, most often a cell, in a defined manner i.e. by overexpression or knockdown of a gene or by addition of a drug and subsequently administering a second set of perturbations and analyzing the system for non-additive readout (i.e. synergistic/antagonistic or synthetic lethality/synthetic rescue) [3].

These perturbation experiments have traditionally been performed in model organisms such as yeast where genetic manipulation is relatively easy compared to mammalian cells [2]. Now, with the advent of technologies including RNA interference (RNAi) and the recent emergence of nuclease-based genome engineering, human cells can also be used to perform functional genomic screens. Cellular fitness, often represented by cell number, division rate or death, is used as a proxy for many of these screens since it is a parameter that can be measured with relative ease. This proxy is also of particular relevance in case genetic interactions are sought as potential anti-cancer therapies. Here, the aim is to kill only cells carrying cancer mutations by targeting an interacting gene which is in synthetic lethal configuration to the mutation. This can be achieved by targeting this second gene product with a small molecule inhibitor or antibody. The non-cancer cells would remain unaffected from this therapy as inhibiting only one interaction partner will not lead to lethality. Indeed, many cancer mutations can be tested systematically against drugs to uncover selective resistance/sensitivity mechanisms, or against small interfering RNAs to find potential new drug targets [4–6].

*A*and

*B*the number of measurements and statistical tests

*T*required to evaluate all unique pairwise combinations is given by:

In practice, the number of data points typically generated is further increased to T x n by the requirement of n replicate measurements. Thus, a screen of, for example, 100 genes against 100 drugs measured in quadruplicate requires 40,000 measurements. A Dataset of this size is usually beyond the limits of what can be conveniently analyzed without the use of dedicated statistics software.

To generate these large datasets, multiplexing strategies greatly improve the throughput of the experiment, by combining genetic perturbations in a single well (multiplexing drug treatments is typically not feasible). A convenient multiplexing strategy is to introduce DNA barcodes into the genome of mutant cell lines such that each genetic perturbation corresponds to a single barcode sequence. In this scenario DNA barcodes act both as unique identifiers for each genetic perturbation and as a proxy for cell number/fitness. Barcodes can be encoded by short hairpin (sh)RNA sequences themselves or introduced into the genome as non-transcribed DNA sequences using lentiviral vectors [7, 8]. Practically, a set of barcoded cell lines (A) can then be pooled together and divided into aliquots that are then screened against the second set (B) of perturbations.

- (1)
Luminex xMAP – a hybridization based multiplexing technology that allows up to 500 measurements in a single sample. Here, DNA barcoded panels consisting of genetically modified cell lines (i.e. expressing an oncogene or knockdown of a tumor suppressor gene) and an unmodified control from the same genetic background are pooled in a single well of a multiwell plate (genetic perturbation, set A) and treated with either a drug or a second genetic perturbation (drug perturbation, set B). In this case only perturbation set A is multiplexed.

- (2)
Massive Parallel Sequencing (MPS). In this case, a panel of non-barcoded cell lines carrying perturbation set A from (1) are infected with a library of lentiviral shRNA vectors (genetic perturbation, set B). Here, the shRNA sequence that integrate into the genome serves both as perturbation and as DNA barcode. Further multiplexing can be achieved by indexing the second perturbation in a single sequencing run. For example, a MPS run yielding 10

^{8}aligned reads on average allows 100 cell lines to be screened against 100 drugs at a reasonable average sequencing depth of 10,000 reads per DNA barcode.

## Implementation

### Programming Language, external software and system requirements

TOPS was developed as a graphical user interface for an analysis pipeline that we originally developed in R. In order to make these R scripts accessible to non-expert users, in particular scientists with little background in scripting languages, we took advantage of the R package rJava (http://www.rforge.net/rJava/) to run the scripts from a Java based interface. TOPS can therefore run its R scripts on all platforms for which rJava is available (currently MacOS, Linux and Windows).

Output from the R interface, including and error messages, is stored in text files for troubleshooting. The overall progress of a session can be monitored and is logged separately.

### User skills and installation

Installation of TOPS consists of unpacking the zipped file into a directory. For TOPS to run, Java, R and the package rJava are must also be installed. Upon first launch, definition of the paths in which R and rJava are located may be required. The most common locations for MacOS, Linux and Windows are checked automatically and the user will be prompted only if the libraries cannot be found. For convenience, alternative locations to be checked in this manner can be added in libPaths.txt in the TOPS directory.

TOPS uses a single semicolon separated values (CSV) data input file. This file has to be generated by the user and can for instance be exported from a Microsoft Office Excel spreadsheet. Alternatively the example datasets can be used for testing. To use TOPS no scripting skills are necessary.

## Results and discussion

### Example datasets provided

TOPS comes with two datasets to test the different procedures. Thus, users can explore the software without having to generate original data.

#### Example dataset 1: a gene-drug interaction screen in breast cancer

To simulate oncogenic events in breast cancer we created a panel of 70 different isogenic cell lines ectopically expressing oncogenes or knocking down tumor suppressor genes commonly found in breast cancer. Findings based on this dataset have been published previously [7].

For multiplexing purposes, each cell line was infected with a vector introducing a genetic barcode (xMAP tag) into the genomic DNA. The cell lines were then pooled, distributed among multi-well plates and treated with 87 individual drugs. After a period of exponential growth, genomic DNA was harvested and barcodes were quantified using Luminex xMAP beads. Raw bead data was converted to median measurements per interaction by calculating the truncated mean. The resulting data is in the format ‘Cell line (name)’, ‘Drug (name)’, ‘Barcode score (numerical)’. The barcode score is a measure of the relative fitness as it is an estimate of the total number of cells for each isogenic cell line under the drug treatment condition.

#### Example dataset 2: a gene-gene interactions screen in breast cancer

We screened 27 isogenic cell lines expressing oncogenes against a library consisting of approximately 400 shRNA vectors covering 80 deubiquitinating enzymes (DUBs). DUBs represent an emerging class of cancer targets involved in many different cellular processes with therapeutic potential. After a period of exponential growth cells were harvested and genomic DNA was extracted in order to PCR-amplify the shRNA barcode cassettes. During the amplification process primers with 60 unique barcode sequences corresponding to the 27 cell lines in 4 replicates were used as described in [9]. The tagged PCR samples were then pooled, a sequencing library was generated and the samples were sequenced on two lanes (50 basepairs) of a Hiseq 2000 instrument (Illumina). The MPS raw data were converted to FASTQ format and split according to the indexing PCR primers with a custom Python script. Each sample’s NGS reads were aligned to the shRNA sequences using shALIGN [10] allowing for zero, one, and two mismatches. The output CSV file is in the format: ‘Cell line (name)’, ‘shRNA (name)’, ‘number of reads’. Number of reads corresponds to shRNA abundance and this is the readout for relative fitness.

#### Importing data

A typical input file consists of five columns with the following information:

perturbation A; perturbation B; fitness score; replicate 1; replicate 2

In the provided example dataset 1, perturbation A corresponds to the gene (i.e. overexpression or knockdown) and perturbation B is a drug treatment. For dataset 2, perturbation B is an shRNA vector targeting a specific DUB and perturbation A is the gene. Fitness score represents the barcode abundance in these examples. Replicates 1 and 2 designate if measurements are replicates of each other. Replicate 1 identifies multiple perturbations towards the same outcome (i.e. multiple different hairpins for one gene, multiple vectors encoding the same cDNA) while replicate 2 identifies the replicate number for a given A-B combination.

TOPS has custom importers covering both types of files from the example datasets. These importers convert the data coming from Luminex or MPS to the input file format.

Entries with non-unique identifiers for perturbation A and perturbation B are automatically interpreted to be replicate measurements by the importers.

#### Pre-analysis filtering

#### Analysis algorithms

TOPS is supplied with two analysis models that are well suited for interaction data of the type that is supplied in the example datasets. However, custom analysis methods can be conveniently plugged into TOPS. The first method is based on a multiple linear regression model and the second one is based on the Mann-Whitney U Test.

#### Statistical analysis: linear model

Linear models have been used previously to normalize [12, 13] and analyze [14, 15] high-throughput measurements. Accordingly, our analysis is composed of two consecutive linear models: the first one is used for data normalization; the second one identifies outliers that represent "hits" i.e. potentially biologically meaningful interactions that warrant further study.

*intensity*

_{ i }as determined by barcode quantification (via MPS or Luminex) are constituted of four components:

- 1)
the systematic effect of perturbation A on fitness

- 2)
the systematic effect of perturbation B on fitness

- 3)
the signal that is due to the (synergistic) combination of perturbation A and B consistent across biological replicates, which is the signal of biological interest

- 4)
noise caused by biological and technical variability between the replicates.

where *intensity*_{
i
} represents the measured fitness score, *β*_{
A
}, *β*_{
B
} are regression coefficients, *A*, *B* are categorical variables representing perturbations A and B respectively, and *s*_{
i
} is a remaining signal including both noise (biological and technical) and a potential synergistic contribution of A and B perturbations. The model is fit to the experimental data to estimate the first two components from the fitness score corresponding to the systematic, non-synergistic perturbations induced by A and B. The linear model was fit by robust regression using an M estimator (function rlm in R library "MASS") to avoid influence of outliers.

*s*

_{ i }to identify potential synergy. Since we want to analyze the effect of each perturbation on the other one,

*s*

_{ i }is dissected twice by fixing either the perturbation A or B first. Namely, fixing A first, we can reduce

*s*

_{ i }to the signal observed for each successive value of A, which we denote by

*s*

_{i|A}. On this reduced data, the effect of perturbation B is estimated by the model:

*A*,

*B*are categorical variables as above,

*β*

_{B|A}the regression coefficient, and

*ε*a term capturing the contribution of noise. The same procedure is applied when perturbation B is fixed first:

The coefficients of these linear models (*β*_{A|B} and *β*_{B|A}) capture the effect of a perturbation within the context of a specific other perturbation. The coefficients combine the signal of replicate experiments and estimate the magnitude of the biological effect thanks to the noise component *ε*.

The ‘rlm’ function of the R ‘MASS’ library is employed to compute a robust estimate of the coefficients of the linear model. This function also offers the possibility to calculate the statistical significance of each coefficient by performing a one-sided t-test (*β*_{A|B} ≠ 0 or *β*_{B|A} ≠ 0). For small sample sizes this test can suffer from false positives due to underestimating variance as described in Axelsson et al. [16].

As both linear models are applied after log transformation of the input data these additive coefficients reflect modeling a multiplicative effect of the fitness response of the pairwise fitness effects *β*_{
A
}and *β*_{
B
} [17, 18].

In the case of the sLM split linear model aimed at reducing computation time and memory usage, the dataset is subdivided into groups of 50 perturbations (A and B), resulting in less data points available for the t-test, hence the reduced statistical power.

#### Statistical analysis: Mann-Whitney U-test

The second method we implemented to analyze fitness score data is based on the *Mann-Whitney U-test*, a more robust alternative to the *Student’s t-test* that does not assume a normal distribution. For this analysis a distinct normalization procedure is employed.

Here, *i* and *j* represent row and column positions in the matrix, and *A*_{
j
} and *B*_{
i
} represent sets containing all values for row *j* and column *i,* respectively. Thus, each value in a row is divided by the corresponding row median, and each value in a column by the column median across the matrix. Each fitness score in the matrix is subsequently log_{10} transformed.

Next, the algorithm performs two-sided tests to calculate p-values. The model requires at least 3 replicates per interaction to perform this test. As with the linear method algorithm we calculate two p-values for each interaction, corresponding to perturbation set A or B.

#### Combining p-values

#### Importing analyzed data into the "results browser" and generating plots

Once data has been analyzed by either method, the results of the analysis are stored in a text file in the following format:

perturbation A; perturbation B; relative magnitude A; relative magnitude B; absolute magnitude A; absolute magnitude B; p-value A; p-value B; combined p-value by Brown’s Method.

Where perturbation A and B are the identifiers for the tested perturbations, relative magnitude A and B gives an indication of the ratio of treatment versus the median of all treatments (control), absolute magnitude A and B are the raw signals from the assay and the p-values are calculated as discussed previously. Given this format, other datasets not generated with our analysis pipeline can also be imported, filtered and plotted using TOPS.

#### Post-analysis filtering

#### User modules

#### Comparison of performance of the analysis models

In order to compare the performance of all three models (linear, split-linear, and Mann-Whitney U-test) we generated a randomized dataset with a distribution based on dataset 1. In this set we generated true positive hits with an average signal of 0.5, 0.7 (reduced fitness) 1.3 and 1.5 fold (increased fitness) compared to the average of true negatives.

**Experimentally validated true and false positive hits from dataset 1**

Model (pvalue) | True positives | False positives | Unverified |
---|---|---|---|

LM (pvA) | 8 | 2 | 40 |

LM (pvB) | 1 | 1 | 48 |

LM (pvAll) | 6 | 2 | 42 |

sLM (pvA) | 8 | 2 | 40 |

sLM (pvB) | 2 | 0 | 48 |

sLM (pvAll) | 8 | 1 | 41 |

UT (pvA) | 7 | 2 | 41 |

UT (pvB) | 4 | 2 | 44 |

UT (pvAll) | 6 | 2 | 42 |

#### Data visualization

## Conclusions

We present a user-friendly software package to analyze and visualize interaction data from functional genomic dual perturbation screens. Although multiple tools for analyzing cell viability screens are available [16, 21–24] these have their limitations by either being based on commercial software (mostly MATLAB) or requiring command line skills. TOPS incorporates statistical models designed for the analysis of pairwise interactions of larger gene/drug sets. Furthermore it is fully based on free software and provides a graphical user interface. The software is easily accessible and offers a powerful analysis tool for the benchtop scientist while being expandable enough to be attractive to users who would like to run their own analysis methods. Importantly, not only Luminex xMAP and Sequencing data can be analyzed with the presented methods but in principle any data from other technologies can be imported as long as the data can be reduced to a "perturbation A", "perturbation B", "score" format and true positives are relatively rare in comparison to true negatives which is a necessity due to the nature of normalization of the in-built analysis. We have included two analysis pipelines based on different methods to demonstrate the versatility of TOPS. We have also included two importers for Luminex xMAP data and for pre-processed screening data that makes these two technologies particularly easy to use with the software.

## Availability and requirements

**Project name:** TOPS.

**Project home page:** https://sourceforge.net/p/topscemm/wiki/Home/.

**Operating system(s):** Win32/OSX/Linux.

**Programming language:** Java and R.

**Other requirements:** Java 6 or newer. R 2.14 or newer.

**License:** Creative Commons Attribution ShareAlike License V3.0.

**Any restrictions to use by non-academics:** Only those imposed by the license.

## Notes

## Declarations

### Acknowledgements

We would like to thank Luminex Corp. for support with the Luminex assay, Helen Pickersgill for help in the preparation of this manuscript, and colleagues from CeMM who acted as beta-testers for the software.

## Authors’ Affiliations

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