Minimizer Revolution Continues with KMC-2 K-mer Counter

Minimizer Revolution Continues with KMC-2 K-mer Counter

This paper had been quite expected from either the KMC or DSK group, based on the success of minimizers so far (check

  • 2014 The Year of Minimizers in Bioinformatics”). The issue is how to choose the minimizer, because alphabetical ordering creates a number of problems. Firstly, the sizes of partitions are unbalanced and low-entropy sequences like AAAAAA get too many hits. Rayan Chikhi et al. showed that choosing minimizers based on relative frequency of presence worked better, but that would require knowing all k-mers, whereas in k-mer counting one attempts to find the k-mers in the first place. Wood and Salzberg came up with another clever approach based on randomizing the bits using XOR.

This paper proposes two novel ideas -

There are two main ideas behind these improvements. The first is the use of signatures of k-mers that are a generalization of the idea of minimizers (Roberts et al., 2004a,b). Signatures allow significant reduction of temporary disk space. The minimizers were used for the first time for the k-mer counting in MSPKmerCounter, but our modification significantly reduces the main memory requirements (up to 35 times) as well as disk space (about 5 times) as compared to MSPKmerCounter. The second main novelty is the use of (k, x)-mers (x > 0) for reduction of the amount of data to sort. Simply speaking, instead of sorting some amount of k-mers we sort a much smaller portion of (k + x)-mers and then obtain the statistics for k-mers in the postprocessing phase.

We are still in the middle of going through the paper, but presume the second idea possibly came from their earlier paper on compression mentioned in our earlier blog post - Minimizer Success Disk-based Genome Sequencing Data Compression. In the meanwhile, please feel free to comment on -

KMC 2: Fast and resource-frugal k-mer counting

Motivation: Building the histogram of occurrences of every k-symbol long substring of nucleotide data is a standard step in many bioinformatics applications, known under the name of k-mer counting. Its applications include developing de Bruijn graph genome assemblers, fast multiple sequence alignment and repeat detection. The tremendous amounts of NGS data require fast algorithms for k-mer counting, preferably using moderate amounts of memory.

Results: We present a novel method for k-mer counting, on large datasets at least twice faster than the strongest competitors (Jellyfish~2, KMC~1), using about 12\,GB (or less) of RAM memory. Our disk-based method bears some resemblance to MSPKmerCounter, yet replacing the original minimizers with signatures (a carefully selected subset of all minimizers) and using (k,x)-mers allows to significantly reduce the I/O, and a highly parallel overall architecture allows to achieve unprecedented processing speeds. For example, KMC~2 allows to count the 28-mers of a human reads collection with 44-fold coverage (106\,GB of compressed size) in about 20 minutes, on a 6-core Intel i7 PC with an SSD.

And the world cup goes to Gliwice and Lodz, Poland !

The presented KMC 2 algorithm is currently the fastest k-mer counter, with modest resource (memory and disk) requirements. Although the used approach is similar to the one from MSPKmerCounter, we obtain an order of magnitude faster processing, due to the following KMC features: replacing the original minimizers with signatures (a carefully selected subset of all minimizers), using (k, x)-mers and a highly parallel overall architecture. As opposed to most competitors, KMC 2 worked stably across a large range of datasets and test settings.

Written by M. //