The main website for cufflinks is here
NOTE: If you're looking for old releases of Cufflinks, including source, you can find them here.
Cufflinks assembles transcripts, estimates their abundances, and tests for differential expression and regulation in RNA-Seq samples. It accepts aligned RNA-Seq reads and assembles the alignments into a parsimonious set of transcripts. Cufflinks then estimates the relative abundances of these transcripts based on how many reads support each one, taking into account biases in library preparation protocols.
Cufflinks was originally developed as part of a collaborative effort between the Laboratory for Mathematical and Computational Biology, led by Lior Pachter at UC Berkeley, Steven Salzberg's computational genomics group at the Institute of Genetic Medicine at Johns Hopkins University, and Barbara Wold's lab at Caltech. The project is now maintained by Cole Trapnell's lab at the University of Washington.
Cufflinks is provided under the OSI-approved Boost License
To get the latest updates on the Cufflinks project and the rest of the "Tuxedo tools", please subscribe to our mailing list
In order to make it easy to install Cufflinks, we provide a few binary packages here to save users from the occasionally frustrating process of building Cufflinks, which requires that you install the Boost libraries. To use the binary packages, simply download the appropriate one for your machine, untar it, and make sure the cufflinks,cuffdiff and cuffcompare binaries are in a directory in your PATH environment variable.
In order to build Cufflinks, you must have the Boost C++ libraries (version 1.47 or higher) installed on your system. See below for instructions on installing Boost.
If you are on Mac OS X, type (all on one line):
bjam --prefix=<YOUR_BOOST_INSTALL_DIRECTORY> --toolset=darwin architecture=x86 address_model=32_64 link=static runtime-link=static --layout=versioned stage installIf you are on a 32-bit Linux system, type (all on one line):
bjam --prefix=<YOUR_BOOST_INSTALL_DIRECTORY> --toolset=gcc architecture=x86 address_model=32 link=static runtime-link=static stage installIf you are on a 64-bit Linux system, type (all on one line):
bjam --prefix=<YOUR_BOOST_INSTALL_DIRECTORY> --toolset=gcc architecture=x86 address_model=64 link=static runtime-link=static stage installUnpack the Cufflinks source tarball (in this example for version 2.2.1):
tar zxvf cufflinks-2.2.1.tar.gzChange to the Cufflinks directory:
cd cufflinks-2.2.1git clone https://github.com/cole-trapnell-lab/cufflinks.git
cd cufflinks
autoreconf --installThe above will generate the configure script.
If Boost is installed somewhere other than /usr/local, you will need to tell the installer where to find it using the --with-boost option. Specify where to install Cufflinks using the --prefix option.
./configure --prefix=/path/to/cufflinks/install --with-boost=/path/to/boost --with-eigen=/path/to/eigenIf you see any errors during configuration, verify that you are using Boost version 1.47 or higher, and that the directory you specified via --with-boost contains the boost header files and libraries. See the Boost Getting started page for more details. If you copied the SAM tools binaries to someplace other than /usr/local/, you may need to supply the --with-bam configuration option. Finally, make and install Cufflinks.
make
make installcufflinks ./test_data.samYou should see the following output:
[bam_header_read] EOF marker is absent. The input is probably truncated. [bam_header_read] invalid BAM binary header (this is not a BAM file). File ./test_data.sam doesn't appear to be a valid BAM file, trying SAM... [13:23:15] Inspecting reads and determining fragment length distribution. > Processed 1 loci. [*************************] 100% Warning: Using default Gaussian distribution due to insufficient paired-end reads in open ranges. It is recommended that correct paramaters (--frag-len-mean and --frag-len-std-dev) be provided. > Map Properties: > Total Map Mass: 102.50 > Read Type: 75bp x 75bp > Fragment Length Distribution: Truncated Gaussian (default) > Estimated Mean: 200 > Estimated Std Dev: 80 [13:23:15] Assembling transcripts and estimating abundances. > Processed 1 loci. [*************************] 100%
Verify that the file transcripts.gtf is in the current directory and looks like this (your file will have GTF attributes, omitted here for clarity)
test_chromosome Cufflinks exon 53 250 1000 + . test_chromosome Cufflinks exon 351 400 1000 + . test_chromosome Cufflinks exon 501 550 1000 + .
Cufflinks includes a number of tools for analyzing RNA-Seq experiments. Some of these tools can be run on their own, while others are pieces of a larger workflow. The complexity of your workflow depends on what you want to achieve with your analysis. For a complete discussion of how Cufflinks can help you with your analysis, please see our protocol paper. The paper includes a diagram (Figure 2) describing how the various parts of the Cufflinks package (and its companion tool TopHat) fit together. As of version 2.2.0, you can also run Cuffquant and Cuffnorm to make large scale analyses easier to handle. The figure below is an updated version of Figure 2 showing how the two utilities released after the protocol paper appeared fit into the workflow:
You can use Cuffquant to pre-compute gene expression levels for each of your samples, which can save time if you have to re-run part of your analysis. Using Cuffquant also makes it easier to spread the load of computation for lots of samples across multiple computers. If you don't want to perform differential expression analysis, you can run Cuffnorm instead of Cuffdiff. Cuffnorm produces simple tables of expression values that you can look at in R (for example) to cluster samples and perform other follow up analysis.
A number of steps in the Tuxedo package work better if you have pre-existing gene annotations. How you can use these annotations is detailed in our protocol paper. Illumina has kindly provided a large number of annotation packages for commonly used model organisms and humans. You can find these packages [here]({{ site.url }}/igenome_table/index.html).
Cufflinks is an ongoing research project as well as a suite of tools. Here are the papers that describe the science behind the programs. If you use Cufflinks, please cite these papers in your work!
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation Cole Trapnell, Brian Williams, Geo Pertea, Ali Mortazavi, Gordon Kwan, Jeltje van Baren, Steven Salzberg, Barbara Wold, Lior Pachter. Nature Biotechnology, 2010, doi:10.1038/nbt.1621 Note: This is the original Cufflinks paper. Please cite this paper if you use Cufflinks in your work.
Improving RNA-Seq expression estimates by correcting for fragment bias Adam Roberts, Cole Trapnell, Julie Donaghey, John L. Rinn, Lior Pachter. Genome Biology, 2011, doi:10.1186/gb-2011-12-3-r22 Note: This paper describes improvements made to Cufflinks to handle bias in RNA-Seq read coverage. Please cite this paper if you use Cufflinks with the -b option in your work.
Identification of novel transcripts in annotated genomes using RNA-Seq Adam Roberts, Harold Pimentel, Cole Trapnell, Lior Pachter. Bioinformatics, 2011, doi:10.1093/bioinformatics/btr355 Note: This paper describes the RABT assembly algorithm. Please cite this paper if you use Cufflinks in RABT mode in your work.
Differential analysis of gene regulation at transcript resolution with RNA-seq Cole Trapnell, David Hendrickson, Martin Sauvageau, Loyal Goff, John L. Rinn, Lior Pachter Nature Biotechnology, 2012, doi:10.1038/nbt.2450 Note: This paper describes Cuffdiff 2. Please cite this paper if you use Cuffdiff in your work.
Cufflinks builds on many ideas, including some proposed in the following papers: