kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads. It is based on the novel idea of pseudoalignment for rapidly determining the compatibility of reads with targets, without the need for alignment. On benchmarks with standard RNA-Seq data, kallisto can quantify 30 million human reads in less than 3 minutes on a Mac desktop computer using only the read sequences and a transcriptome index that itself takes less than 10 minutes to build. Pseudoalignment of reads preserves the key information needed for quantification, and kallisto is therefore not only fast, but also as accurate than existing quantification tools. In fact, because the pseudoalignment procedure is robust to errors in the reads, in many benchmarks kallisto significantly outperforms existing tools.
kallisto quantified RNA-Seq can be analyzed with sleuth.
Please visit http://pachterlab.github.io/kallisto/manual.html for the manual.
Please read the license before using kallisto. The license is distributed with kallisto in the file license.txt also viewable here.
There is a low traffic Google Group, kallisto-sleuth-announcements where we make announcements about new releases. This is a read-only mailing list.
For help running kallisto, please post to the kallisto-sleuth-users Google Group.
Please report bugs to the Github issues page
We typically develop on separate branches, then merge into devel once features
have been sufficiently tested. devel is the latest, stable, development
branch. master is used only for official releases and is considered to be
stable. If you submit a pull request (thanks!) please make sure to request to
merge into devel and NOT master. Merges usually only go into master, but
not out.