TopHat is a fast splice junction mapper for RNA-Seq
reads. It aligns RNA-Seq reads to mammalian-sized genomes using the
ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons.
TopHat is a collaborative effort among Daehwan Kim and Steven Salzberg in the Center for Computational Biology at Johns Hopkins University, and Cole Trapnell in the Genome Sciences Department at the University of Washington. TopHat was originally developed by Cole Trapnell at the Center for Bioinformatics and Computational Biology at the University of Maryland, College Park.
News and updates
|New releases and related tools will be announced through the Bowtie mailing list.|
Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biology 10:R25.
Kim D and Salzberg SL. TopHat-Fusion: an algorithm for discovery of novel fusion transcripts. Genome Biology 2011, 12:R72
Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, Salzberg SL. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. . Genome Biology 2013, 14:R36
TopHat2 source is available in a public GitHub repository (3/31/2015).
TopHat 2.0.14 release 3/24/2015Version 2.0.14 is a maintenance release with the following changes:
- pipeline speed improvements thanks to contributions from Véronique Legrand and Michaël Pressigout of Institut Pasteur
- added support for xz compressed read files (thanks to a patch submitted by Ashton Trey Belew)
- applied a couple of Python fixes to prevent potential issues with package handling and some file operations
- fixed a potential linking issue where the wrong libbam.a library could have been linked when building from source
TopHat 2.0.13 release 10/2/2014Version 2.0.13 is a maintenance release with the following changes:
- removed SAMtools as an external dependency in order to avoid incompatibility issues with recent and future changes of SAMtools and its code library (an older, stable SAMtools version is now packaged with TopHat)
- fixed a few code compatibility issues when compiling on OSX 10.9
TopHat 2.0.12 release 6/24/2014
Version 2.0.12 is a maintenance release with the following simple fix:
- This version is compatible with Bowtie2 v2.2.3.
TopHat 2.0.11 release 3/4/2014
Version 2.0.11 is a maintenance release with the following simple fix:
- This version is compatible with Bowtie2 v2.2.1, although it does not support a 64-bit Bowtie2 index yet.
TopHat 2.0.10 release 11/13/2013
Version 2.0.10 is a maintenance release with the following fixes and changes:
- Improved support for adding unpaired reads to PE reads in the same TopHat2 run (please see the manual entry for this usage). This includes reporting separate counts for the additional unpaired reads and making sure that the SAM flags in the output files reflect the paired or unpaired origin of the reads.
- Added the possibility to run TopHat just for the purpose of preparing the transcriptome index files (please see the manual entry for this special usage).
- The input read files can have different file formats, as TopHat now autodetects the FASTA/FASTQ format of each input file.
- Fixed a bug that could sometimes incorrectly rename the reads in the output alignments.
- The stats in
align_summary.txtnow reflect the reported mappings under the constraints of the provided Tophat options, instead of reflecting the internally detected alignments. As such, the number of reads with multiple mappings may appear to be incorrectly reported if the user provided options that directly affect the reporting of such multiple mapppings.
- Fixed a bug that caused TopHat to fail when bowtie1 and pre-filtering options were used together.
TopHat 2.0.9 release 6/28/2013
Note (6/29/2013): this version is slightly updated to handle 1-bp exons when using --GTF option.
Version 2.0.9 is a maintenance release providing better management of the transcriptome data files and fixes a few problems found in earlier releases:
- Solved parsing issues with some GFF3 files that could produce a crash with previous versions.
- Starting with this version TopHat2 will automatically check for consistency and, if needed, rebuild the existing transcriptome data files after critical updates of the GFF parser or a detected change of the underlying annotation data (GFF file).
- The output file
unmapped.bamno longer contains multi-mapped reads (reads with too many alignments found), but only reads for which a suitable alignment could not be found under the current alignment constraints.
- A new output file:
align_summary.txtis now generated in the output directory, containing read (pair) input and mapping counts.
- Fixed a bug that added an extra XS tag in the output BAM file.
- Fixed a reporting bug that caused paired reads with a read containing its mate to be reported as unpaired.
- Fixed a bug in bam2fastx utility that caused the -M/--mapped-only option to be ignored (Note: this option is not used within TopHat).
- In tophat-fusion-post: fixed a bug that caused two genes of a fusion gene to sometimes be incorrectly ordered and reported.
TopHat2 paper published 4/25/2013
- The simulation data set (error-free) is available here.
TopHat 2.0.8 release 2/26/2013
Note (4/12/2013): patched version 2.0.8b was released in order to provide compatibility with Bowtie v1.0.0
Version 2.0.8 is a quick fix release addressing the following issues:
- This version correctly handles the newest version of Bowtie2 v2.1.0.
- The segment mapping slow-down introduced by some Bowtie2 parameter changes in version 2.0.7 is now corrected.
TopHat 2.0.7 release 1/23/2013
Version 2.0.7 is a maintenance release addressing some issues found in the earlier releases:
- Please update Bowtie1 or Bowtie2 to the latest released versions (0.12.9 and 2.0.5, respectively). It may be necessary to download the latest Bowtie genome indexes and it is strongly recommended to remove&rebuild the transcriptome indexes.
-i/--min-intron-lenoption now allows introns of length less than 50
--no-mixedoption is now correctly handled. TopHat no longer produces singleton alignments when this option is used.
- Explicit mate pairing information (/1 or /2 suffix) in the read name in unmapped.bam is removed. The SAM flag provides the pairing information.
- TopHat spawned processes which sometimes showed the warning message like "[main_samview] truncated file" are now properly terminated.
- With a large number of reads and --fusion-search enabled, TopHat consumed a huge amount of memory, in particular, in long_spanning_reads program, which is now fixed.
TopHat 2.0.6 release 11/02/2012
Version 2.0.6 is a maintenance release addressing some issues found in the 2.0.5 release:
- corrected the indel finding algorithm that caused segmentation fault in certain cases (long_spanning_reads and tophat_reports)
- fixed the Bowtie version checking code, adding support for newer, non-beta Bowtie2 versions
- several minor fixes in the fusion alignment algorithm
- fixed an incompatibility issue with Python versions older than 2.6 (restoring Python 2.4 compatibility)
- fixed and improved the resuming option (-R/--resume) to better handle various failure/resume situations
- added a warning about Bowtie1 and Bowtie2 index files in the same
directory (causing trouble if they were built for different genomic
TopHat 2.0.5 release 9/18/2012
Version 2.0.5 adds new options to better control the read alignment
and to improve mapping accuracy, and the ability to resume partial
- along with -N/--read-mismatches, TopHat introduces new options for finer
control of the read alignment process by limiting the number of mismatches,
indels and indel length.
Please check new options --read-gap-length and --read-edit-dist.
- the new --read-realign-edit-dist option can be used to greatly improve spliced-mapping accuracy
(especially in the absence of annotation data) by forcing the
re-mapping of some or all reads regardless of them being already mapped
in earlier steps of the pipeline.
- we added the option to resume a TopHat run which was prematurely terminated:-R/--resume <tophat_out>
- --transcriptome-mismatches and --genome-mismatches are now deprecated
TopHat 2.0.4 release 6/21/2012
Version 2.0.4 is a maintenance release addressing some issues found in the 2.0.3 release:
- Fixed a bug that caused the last stage of TopHat (tophat_reports) to occasionally crash for large data sets.
- For paired reads found to be incorrectly paired in the input
files TopHat now outputs a warning message instead of terminating with
- Alignments of paired reads mapped discordantly (e.g. on different
chromosomes) are now reported by default. To disable this behavior,
--no-discordant option can be used. Also please check --no-mixed option
in the manual, which we borrow from Bowtie2 options.
- --fusion-search with Bowtie2 is still in developmental stage, it may require much memory space and produce many spurious fusions. You may want to try a combination of --bowtie1 and --fusion-search if it does not work.
- Environment variables such as BOWTIE_INDEXES and BOWTIE2_INDEXES are handled properly - please refer to the Bowtie website for more details about the variables.
- Prebuilt transcriptome indexes built by older versions of TopHat may not be compatible with this version due to some internal changes in parsing gtf files. It is strongly recommended to build a new transcriptome index.
TopHat 2.0.3 release 5/26/2012
Users are strongly recommended to upgrade to this release as the source distribution and the binary versions of TopHat2.0.2 have some serious issues that cause runtime failure.
iGenomes index and annotation have been updated to include Bowtie2 indexes (in addition to Bowtie1 indexes) - 5/23/2012
TopHat 2.0.2 release 5/23/2012
Version 2.0.2 is a maintenance release:
Note (9:50pm EST - 5/23): this version is slightly updated to remove some debugging code, which caused TopHat to exit abnormally.
- Fixed a bug TopHat2 aborts while reads overlapping with introns are being re-aligned, giving an error message like
./SeqAn-1.3/seqan/sequence/segment_infix.h:81 Assertion failed : data_begin_position <= data_end_position was: 18446744073709551607 > 31
- Some unique alignments were set as secondary alignments using 0x100 SAM flag, which is now fixed.
TopHat 2.0.1 maintenance release 5/17/2012
Version 2.0.1 is a maintenance release addressing some issues found in the 2.0.0 release:
- Fixed the problem with some alignments in the BAM output (accepted_hits.bam) missing quality values.
- The Read Group tag "RG" is now properly written for each alignment when using --rg-id and related options.
- More strict checking for genomic coordinates is performed when retrieving spliced sequences.
- Colorspace reads are now correctly handled (--color option).
- Paired-end input reads are now checked for consistency (proper ordering in the input files).
- Restored the functionality of options --no-sort-bam and --no-convert-bam.
- --transcriptome-only option is correctly processed.
- Some of alignments that overlap with introns are realigned against those corresponding splice sites. If those new alignments are better than the previous alignments, they will be reported.
- If the reference genome and the transcriptome files have the same prefix like genome (genome.fa and genome.gtf), it caused some naming problems for chromosomes, which is now fixed.
- Some of reads not present in neither accepted_hits.bam nor unmapped.bam are now reported correctly.
TopHat 2.0.0 release 4/09/2012
Version 2.0.0 is a major release adding Bowtie 2 support, better parallelization and the ability to align RNA-Seq reads across potential fusion points.
- TopHat now uses Bowtie2 by default (if found in the system)
although it can also fall back on Bowtie 1 (which is still required for
- Bowtie 2 integration features:
- most of the optional SAM fields (AS, MD, NM, and etc.) generated by Bowtie 2 are now reported by TopHat as well (reconstructed as necessary)
- many of the Bowtie 2 options can now be directly given as TopHat options using --b2-<bowtie option name>. These apply to initial read mappings, not to segment mappings - please see the corresponding manual section.
- Most of the time-consuming steps in the TopHat 2 pipeline are
now parallelized, reducing the total running time substantially on
- In addition to mapping across splice sites, TopHat 2 can now
align reads across fusion points,
which usually occur due to genomic translocations, read-through
transcription, or trans-splicing; Tophat 2 integrates the fusion
discovery engine previously found in TopHat-Fusion
(fusion mapping is optional, please see the separate page for fusion mapping and the --fusion-... options in the manual).
- Colorspace (SOLiD) reads require the older version of Bowtie, since Bowtie 2 does not provide support for this kind of reads.
- --closure-search and --butterfly-search options have been deprecated
- In addition to reporting the best (or primary) alignments (the original TopHat behavior), TopHat 2 can report the secondary alignments up to 20 (the default) paired or single alignments (see --report-secondary-alignments and -g/--max-multihits)
- The installation of the Boost package is now required in order to build TopHat 2 from source (see Installation).
- New options affecting TopHat's output:
- --keep-fasta-order (for those who prefer the order of
reference sequences in the SAM output to match the order of the
sequences in the genome fasta file)
- If you had some older versions of TopHat and TopHat-Fusion installed on your system, we suggest that you remove both programs before installing the new version and make sure that your system PATH includes the new version but does not include the other ones.
Important notes - 3/26/2012
For those who want to follow our Nature Protocols, we suggest users use TopHat 1.3.2 (see the download links below) because TopHat 1.4.1 has some problems with running the protocols when mapping some of the simulated reads (e.g., C2_R2). These problems do not happen with real data, so reverting back to TopHat 1.3.2 is not necessary.
- Source code (version 1.3.2)
- Linux x86_64 binary (version 1.3.2)
- Mac OS X x86_64 binary (version 1.3.2)
TopHat and Cufflinks protocol published at Nature Protocols - 3/12/2012
A complete bioinformatic protocol for analysis of RNA-Seq data using our tools has been published at Nature Protocols. The protocol covers read alignment with TopHat, gene and transcript discovery with Cufflinks, annotation analysis with Cuffmerge and Cuffcompare, differential expression analysis with Cuffdiff, and visualization with CummeRbund. Several variants of the protocol are included for those who wish to forgo certain analysis steps, such as gene discovery.
TopHat 1.4.1 release 2/2/2012
Version 1.4.1 is a maintenance release addressing some issues found in the 1.4.0 release:
- fixed a bug that prevented the correct functionality of the new transcriptome mapping option for paired reads in cases where the user only wanted to map to the transcriptome (-T option) or there were no unmapped reads
- fixed the -N/--initial-read-mismatches option to support values larger than 3 (e.g. for mapping on a genome from a different species).
- added basic file checks for extreme cases when there are no initially unmapped reads
TopHat 1.4.0 release 1/5/2012
Version 1.4.0 includes the following new features and fixes:
- when a set of known transcripts is provided (-G/--GTF option) Tophat now takes the approach of mapping the reads on the transcriptome first, with only the unmapped reads being further aligned to the whole genome and going through the novel junction discovery process like before. This new approach was implemented by Harold Pimentel.
- new command line options have been added for the new mapping-to-transcriptome approach; please check their documentation which includes important notes about the new --transcriptome-index option for efficient use of this approach
- the unmapped reads are now reported in the output directory as unmapped_left.fq.z (and unmapped_right.fq.z for paired reads)
- the --initial-read-mismatches value now also applies to final alignments resulted from joining segment mappings
- we adjusted the selection of hits to be reported in case of multi-mapped segments, reads and read pairs
- enhancements in junction discovery for the segment-search method in the case of paired-end reads
- the reported running time now includes days
- fixed the non-deterministic behavior that could cause some differences in the output of repeated Tophat runs
- fixed a regression bug that prevented the use of SOLiD reads with certain length of quality values
TopHat 1.3.3 release 10/16/2011
Version 1.3.3 is primarily a bug-fix release:
- fixed a bug that prevented coverage search from being activated on short reads (with fewer than 3 segments, e.g. reads shorter than 75)
- fixed a samtools path inconsistency that in some system configurations caused tophat to exit with an error in the final stage, when sorting the "accepted_hits.bam" file
- for SOLiD reads, quality value strings should now be accepted with or without a primer value
TopHat 1.3.2 release 9/5/2011
Version 1.3.2 includes the following fixes and improvements:
- Deprecated -r as a required parameter (defaults to 50)
- Tophat no longer requires named pipes (mkfifo) to work, which were used in the previous version to compress some of the temporary files, but was not supported on some file/systems; for systems supporting mkfifo the new -X option can be used to re-enable this functionality
- coverage-search is now working for a short read (e.g., <40-bp) where a read is split into only one segment.
iGenomes index and annotation packages available for download - 7/31/2011
Illumina has generously provided a set of freely downloadable packages that contain everything you need to get started working with TopHat and Cufflinks. These packages contain Bowtie indexes for the human, mouse, and fly genomes as well as many others. The packages also contain annotation files (in GTF format) from UCSC, Ensembl, NCBI, and other sources. These files are augmented with the special attributes Cufflinks needs to perform differential splicing and promoter analysis. We strongly encourage users to download and try these packages!
TopHat 1.3.1 release 6/23/2011
Version 1.3.1 includes the following bug fixes and changes.
- Quality value strings beginning or ending with "*" are no longer truncated to a single quality value "*" in accepted_hits.bam
- SOLiD reads that have "!" (or 0) as the first quality value caused a runtime error, which is now fixed
- --closure-search is compatible with internal file compression
- --max-deletion-length option is correctly handled
- A new option --initial-read-mismatch option is introduced that users specify the number of mismatches allowed in the initial read mapping
- For short reads (usually <45-bp), it is recommended that users decrease segment length (--segment-length) to about half the read length and segment mismatches (--segment-mismatches) to 0 or 1
- TLEN field in SAM format is correctly output
- Indel search has been turned on (by default) since TopHat 1.3.0 - users can disable the functionality using --no-novel-indels
TopHat 1.3.0 release 6/2/2011
Note (10:30 EST): the binary packages for 1.3.0 have been updated to correct a hardcoded python path.
This release includes some very substantial performance improvements, bug fixes, and enhancements.
- Geo Pertea has restructured the internal workflow of TopHat so that nearly all temporary data is compressed during a run. This greatly reduces the on-disk footprint of TopHat runs, and also reduces the amount of disk I/O. These enhancements should improve running time on networked filesystems.
- Thanks to contributions from the Picard team (notably Alec Wysoker at the Broad Institute), TopHat has some needed SAM compliance fixes and some additional command line options that make it easier to incorporate TopHat into sequencing core workflows and automated processing pipelines.
- TopHat can optionally use Bowtie's -n flag as an alternative to the read mapping protocol. The default is still to use -v, which can result in better spliced alignment accuracy when reads contain relatively few sequencing errors (particularly at the 3' end)
- TopHat now supports both GTF2 and GFF3
- TopHat can take gzip or bzip2 compressed FASTQ or FASTA files as input, decompressing them on the fly (the decompression program is determined based on the file name suffix)
- The initial read inspection stage, used to determine the format, read length and other parameters needed for the run, is now significantly faster.
- A bug in the installer caused the tophat script to be duplicated (apparently without causing further problems). Thanks to John Marshall for the fix to this and several other issues.
- Numerous other minor bug fixes
TopHat-Fusion 0.1.0 (Beta) release 5/09/2011
TopHat-Fusion is released, mainly developed by Daehwan Kim and Steven Salzberg. TopHat-Fusion is an enhanced version of TopHat with the ability to align reads across fusion points, which results from the breakage and re-joining of two different chromosomes, or from rearrangements within a chromosome. For more information, please visit the TopHat-Fusion website.
New "Getting Help" email address for TopHat and Cufflinks
In order to more effectively answer user help requests and improve usability and documentation, we have created an email address to which users can send messages for technical support. If you have questions about Cufflinks or TopHat, please send them to firstname.lastname@example.org. We will do our best to answer your question in a timely fashion, although please read the manual carefully before sending your email. We have very limited time to answer questions, and most questions require careful, technical answers.
If you believe you have found a bug in the software, please include a small package of test data with your email so that we can reproduce your problem locally. A test example makes it much easier to correct the issue.
TopHat 1.2.0 release 1/18/2011
Version 1.2.0 includes some important bug fixes as well as a major new feature. Thanks to the efforts of Ryan Kelley from Illumina, TopHat now supports detection of insertions and deletions using RNA-Seq data. TopHat will report reads aligned across discovered indels by taking advantage of I and D CIGAR operators as specified by the SAM format. For convenience, the indels discovered during each run are also reported in BED files, similar to the junctions.bed file that TopHat reports for splice junctions.
Version 1.2.0 also addresses the following issues:
- A problem with alignment of reads of mixed length has been fixed. Users with a wide range of read lengths, such as trimmed 454 data sets, are strongly encouraged to upgrade.
- A compatibility issue with samtools version 0.1.12a has been fixed.
- Runtime validation of input files (e.g. raw junctions files) has been improved.
TopHat and Cufflinks now supported through Galaxy
We are very pleased to announce that you can now run TopHat and Cufflinks through Galaxy. The Galaxy project aims to make informatics tools accessible through the web, and allows you to experiment with parameter settings and create sophisticated analysis workflows easily. Galaxy is developed by researchers at Emory University and Penn State in the Taylor and Nekrutenko labs, respectively. We are extremely grateful for the Galaxy team's work, and proud to have TopHat and Cufflinks offered through their platform.
TopHat 1.1.4 release 11/16/2010
Version 1.1.4 includes three important bug fixes:
- Another issue related to strand assignment in strand specific libraries has been fixed
- A limitation in aligning long reads has been overcome, substantially improving overall alignment sensitivity
- The --gtf-annotations was throwing an error during prep_reads due to a bug in internal command line parsing.
Several users pointed out that the recently released version 1.1.3 had "1.1.0" listed in the version number on running TopHat. This has been corrected in the 1.1.4 build.
TopHat 1.1.3 release 11/13/2010
This is a strongly recommend fix release of TopHat. Version 1.1.2 suffered from a bug related to the addition of strand specific read processing that could result in some reads being incorrectly assigned to the wrong strand. This bug affected users of unstranded RNA-Seq data as well as users of stranded reads, so 1.1.3 is a recommended update for all users.
TopHat 1.1.2 release 10/26/2010
This release of TopHat adds support for strand-specific RNA-Seq alignment for reads produced by a number of strand-specific protocols. Please see the manual for details. This release also supports variable-length reads. Version 1.1.2 also fixes several bugs
- A sorting issue for pairs that align in multiple places has been fixed.
- Some portability issues, which resulted in segfaults on some systems, have been fixed in the precompiled binaries.
TopHat 1.1.1 release 10/11/2010
This release of TopHat includes some fixes related to Colorspace read mapping.
- Negative quality values are now handled correctly.
- Comments at the beginning of csfasta files no longer trigger an error.
- --integer-quals no longer conflicts with -i
- The header in TopHat BAM files now correctly lists the sort order as coordinate, with group order reference
Update - TopHat 1.1.0 packages
The build of 1.1.0 released yesterday was throwing an exception with single end reads. This has been corrected and the packages have been updated.
New developers - Daehwan Kim and Geo Pertea
The TopHat team has been joined by Daehwan Kim and Geo Pertea. Daehwan is a Ph.D. student at the Center for Bioinformatics and Computational Biology (CBCB), working with Steven Salzberg. He is principally responsible for extending TopHat to support SOLiD sequencing reads. Geo is an informatics engineer at CBCB, and has made numerous contributions to Cufflinks along with a number of other tools built at CBCB.
TopHat 1.1.0 release 10/03/2010
This release of TopHat includes some major enhancements:
- TopHat now supports Colorspace reads from Life Technologies' SOLiD sequencer, thanks to the efforts of Daehwan Kim and Geo Pertea. Note that you will need to download a Colorspace Bowtie index to use TopHat with SOLiD reads. Colorspace Bowtie indices typically have "_c" in their name to distinguish them from nucleotide space indices.
- Alignments are now reported in BAM instead of SAM. This requires installation of the SAM tools.
- GFF3 support has been dropped in favor of GTF. If you are working with an organism that is well annotated, we recommend supplying a GTF from Ensembl or UCSC to maximize spliced alignment sensitivity. TopHat will augment the annotated junctions with those it finds during each run.
- TopHat no longer outputs the wigglegram after each run, as browsers such as IGV, IGB and UCSC can display BAM files directly.
TopHat 1.0.14 (BETA) release 6/30/2010
This fix release includes a new FASTQ parser (written by Geo Pertea) and generally improves error checking and reliability.
TopHat 1.0.13 (BETA) release 2/5/2010
This is a fix release that addresses several bugs. Notably:
- SAM quality strings are now reported on the Phred scale, regardless of whether the input reads were in Phred or Solexa scaling, as require by the SAM spec. The conversion code in qual.h/.cpp was written by Ben Langmead and is borrowed from Bowtie.
Bowtie index update 11/14/2009
In response to user requests, Ben Langmead was kind enough to rebuild the Bowtie indexes for human and mouse from UCSC assembly fasta files. Because UCSC fasta files have simple record names, such as "chrX", TopHat runs against them are easier to visualize with the UCSC genome browser or the Integrative Genomics Viewer. We recommend that users who need indexes other than human or mouse build them from UCSC fasta files.
TopHat 1.0.12 (BETA) release 10/28/2009
This release includes both critical fixes and new features, including:
- A serious bug that hurts sensitivity for short (~36bp) reads that was introduced in 1.0.11 has been fixed
- TopHat now automatically deletes the intermediate files it produces during each run, which can be very large. You can preserve them by specifying --keep-tmp at the beginning of a run.
- A new optional search algorithm for short (~36bp) reads, designed to improve junction detection sensitivity, is now available with --butterfly-search.
- TopHat no longer calculates gene expression. Users interested in expression calculations should consider using Cufflinks for gene- and isoform-level expression calculations.
- Numerous performance enhancements and reductions in memory usage. For reads 75bp or longer, memory usage is dramatically lower, and should scale much for runs with hundreds of millions of reads.
- The manual has been updated to better describe the types of reads TopHat expects. The manual also incorrectly stated that TopHat doesn't look for "GC-AG" and "AT-AC" introns, and this has been corrected.
IMPORTANT - Bowtie update 10/13/2009
Until recently, there was a bug that could cause TopHat to report no alignments or junctions with some Bowtie indexes (including) some indexes downloadable from this site. All users are strongly encouraged to upgrade to Bowtie 0.11.0 or later, and the next update to TopHat will force this upgrade.
TopHat 1.0.11 (BETA) and Cufflinks release 9/26/2009
We're pleased to announce the release of a sister tool to TopHat, called Cufflinks. TopHat aligns your RNA-Seq reads; Cufflinks assembles those alignments into transcripts and also calculates isoform and gene level expression in your samples.
This TopHat release contains a number of stability improvements, fixes, and some substantial performance increases. The disk footprint is also reduced, though it's still large, and further reductions are coming in future releases.
We advise all users to adopt Cufflinks to compute expression values. Cufflinks contains a sophisticated algorithm for this calculation, that is far more accurate than TopHat's method. In an upcoming release of TopHat, the RPKM calculation in TopHat will be removed to simplify maintenance.
1.0.10 (BETA) release 7/30/2009
This is a fix release. Notable changes:
- More SAM compliance fixes.
- Reduced the frequency of certain types of false junctions through improved spliced alignment filtering
Minor update to 1.0.9 7/10/2009
Version 1.0.9 of TopHat released on 7/8/09 had an incorrect default value for --max-intron length. It is now 500,000, as intended.
1.0.9 (BETA) release - 7/8/2009
This release includes both fixes and new features. This upgrade requires Bowtie 0.10.0.0 or later. Other changes including:
- Substantially improved sensitivity for reads shorter than 75bp
- An optional "gap-filling" phase to map multireads from transcribed repeats
- Fixed some SAM compliance issues
- Optional (limited) search for alignments that involve microexons
- Complex index record names no longer crash the pipeline.
- The command line options have been overhauled, and the meaning of the -a/--min-anchor option has changed. Please see the manual for further details.
- Closure search is now off by default for all read types
- Coverage search is off by default for reads 75bp or longer
- Previous version could report spliced alignments with gaps longer than --max-intron, if any were found. The --max-intron and --min-intron limits are now strictly enforced.
Bowtie updated to 0.10.0.0
IMPORTANT: TopHat 1.0.8 is incompatible with Bowtie 0.10.0.0, which was released this week. While the release of TopHat 1.0.9, which is imminent, will fix the incompatibilities, users are encouraged to stick with Bowtie 0.9.9.3 for now.
1.0.8 (BETA) release - 5/25/2009
This is mostly a fix release, but all users are encourage to upgrade, as some of the bugs fixed were fairly major. Other notable improvements include:
- If you have reads 50bp or longer, TopHat will look for GC-AG and AT-AC introns
- Logging has been improved
- Fewer false positives in gene families with tandem copies
- Some users have reported pipeline crashes when using Bowtie indexes with long or complex record names. This will be fixed in the next release, but for now, using an index with simple names (no spaces or pipes) is a workaround. Users are recommended to use names like "chr12" to avoid problems.
1.0 (BETA) release - 5/4/2009
TopHat has been almost entirely redesigned and rewritten to handle "second-generation" RNA-Seq data. Reads longer than 50bp and paired end reads are substantially more powerful for finding splice junctions, and TopHat needed new algorithms to take advantage of them. While this release should be considered a beta, and still contains bugs, it has been under development for several months and has been tested by several groups on both first- and second-generation RNA-Seq data in multiple organisms. Longer and/or paired end reads provide a dramatic leap in sensitivity and specificity. Notable improvements include:
- Paired-end RNA-Seq read support
- Long read support
- Improved SAM output
- No longer depends on Maq
- Mismatches near splicing anchors now allowed
- Much more of the pipeline is multithreaded, yielding a massive performance boost
- Compiles under GCC 4.3
TopHat paper published - 3/16/2009
0.8.3 release - 3/12/2009
This release contains the following enhancements and fixes:
- Reporting now has a smaller memory footprint
- A possible source of erroneous alignments due to hashing collisions has been eliminated
- The install scripts now correctly detects whether to build TopHat with 64-bit compiler flags.
TopHat paper accepted - 3/1/2009
Our paper on discovering splice junctions has been accepted at Bioinformatics, and should appear soon.
0.8.2 release - 3/1/2009
This release contains the following enhancements and fixes:
- TopHat now reports the alignments it finds in the SAM format. The SAM tools were written primarily by Heng Li at Sanger, and will allow TopHat users to call expressed SNPs from their RNA-Seq reads. The SAM tools themselves are still under development, so TopHat's SAM support should be considered experimental.
- You can now specify a list of junctions for TopHat to check in a raw format, without using a GFF file of genes
- The new -o option allows you to change where TopHat puts its output, instead of always writing to "./tophat_out"
0.8.1 release - 1/30/2009
This release contains the following enhancements and fixes:
- New experimental support for user-supplied annotations. TopHat will accept a GFF file, and will look for junctions contained in the GFF file. TopHat will also perform a basic RPKM calculation on the regions in the annotation, normalized to those annotations only (rather than the whole map). The file must contain "gene", "exon" and "mRNA" records, in the normal record ID, Parent heirarchy. Users are encouraged to treat GFF support as unstable and interpret their results with caution.
- Several minor bugfixes.
0.8.0 release - 1/19/2009
This release contains the following enhancements and fixes:
- Dramatic reduction in false positives.
- TopHat now estimates a minor isoform frequency for each splice junction, and filters infrequent events to cut down dramatically on the false positives. By default, minor isoforms must occur at at least 15 percent of the major isoform.
- The new output file coverage.wig is a UCSC wigglegram of alignment coverage.
- TopHat supports multithreading, though not all stages of the pipeline use multiple threads.
- TopHat now allows reads to have multiple alignments, and it suppresses alignments for reads that have more than a user-specified number (10, by default).
- The memory exhaustion problem associated with converting Bowtie alignments to Maq has been fixed.
- You are no longer required to concatenate your reads into a single input file.
- TopHat will attempt to automatically determine seed length, quality scale, and FASTA/FASTQ format from your input reads.
- If you are missing a Maq binary fasta file for your reference, one will be created in the output directory using bowtie-inspect. You can copy this file to the location of your bowtie index to avoid this step in your next run.
0.7.2 release - 12/05/2008
The following issues have been fixed:
- Bowtie 0.9.8 renamed bowtie-convert to bowtie-maqconvert, and TopHat is now compatible with both the new and old name.
- Minor cosmetic improvements in the TopHat output log.
- Improved checking in the installer to emit sensible error messages when compiling on Solaris. Solaris is currently not supported, but hopefully will be in the next release.
- TopHat can exhaust memory when run with many (> 50 million) reads on some machines. This will be fixed in the next release.
0.7.1 release - 11/08/2008
The following issues have been fixed:
- Maq 0.7.0 changed the Maq map file format. Bowtie 0.9.7 now supports both the new and old mapping format, and thus so now does TopHat. TopHat now checks the version of Maq on the system and uses the correct format.
- Minor command line interface improvements
- The -X option has been added to allow the use of FASTQ files that are scaled on the Solexa quality scale, as opposed to Phred (the default). Note that TopHat doesn't support FASTQ-int, only ASCII-encoded qualities are used.
- The -D option has been added, allowing users to specify when to look for junctions within single islands, as opposed to just between two distinct islands
- The -Q option allows the user to specify a Phred quality character below which the island consensus caller will use the reference base call. That is, TopHat will not allow SNPs to be called where base quality drops below a certain threshold.
- TopHat now includes Heng Li's fq_all2std.pl format conversion script to make installation easier.
0.7.0 release - 10/27/08
The first public release of TopHat is now available for download. To use TopHat, you will need to install Bowtie and Maq. Both are open source and freely available under the Artistic license. When you install Bowtie, you should also install the Bowtie index for the genome in your RNA-Seq experiment, if one is available. If there is no pre-built index for the organism you're interested in, you can follow the Bowtie manual's section on how to build one yourself.
Because this is the first release, the manual is very limited. Only the basic options have been described. However, we will be updating it frequently, so please check back. If you find something unclear, or have questions about how TopHat works, please email Cole Trapnell. We will be posting a list of frequently asked questions soon.
In this release, TopHat does not consider mate pairing between reads. You can analyze paired-end RNA-Seq data with TopHat, but the program won't make use of the mate information. Yet. Use of mate pair information is our top development priority. Check back soon for a release with full paired-end support