Getting Started

```sh git clone https://github.com/lh3/minimap2 cd minimap2 && make

long sequences against a reference genome

./minimap2 -a test/MT-human.fa test/MT-orang.fa > test.sam

create an index first and then map

./minimap2 -x map-ont -d MT-human-ont.mmi test/MT-human.fa ./minimap2 -a MT-human-ont.mmi test/MT-orang.fa > test.sam

use presets (no test data)

./minimap2 -ax map-pb ref.fa pacbio.fq.gz > aln.sam # PacBio CLR genomic reads ./minimap2 -ax map-ont ref.fa ont.fq.gz > aln.sam # Oxford Nanopore genomic reads ./minimap2 -ax map-hifi ref.fa pacbio-ccs.fq.gz > aln.sam # PacBio HiFi/CCS genomic reads (v2.19+) ./minimap2 -ax lr:hq ref.fa ont-Q20.fq.gz > aln.sam # Nanopore Q20 genomic reads (v2.27+) ./minimap2 -ax sr ref.fa read1.fa read2.fa > aln.sam # short genomic paired-end reads ./minimap2 -ax splice ref.fa rna-reads.fa > aln.sam # spliced long reads (strand unknown) ./minimap2 -ax splice -uf -k14 ref.fa reads.fa > aln.sam # noisy Nanopore direct RNA-seq ./minimap2 -ax splice:hq -uf ref.fa query.fa > aln.sam # PacBio Kinnex/Iso-seq (RNA-seq) ./minimap2 -ax splice --junc-bed=anno.bed12 ref.fa query.fa > aln.sam # use annotated junctions ./minimap2 -ax splice:sr ref.fa r1.fq r2.fq > aln.sam # short-read RNA-seq (v2.29+) ./minimap2 -ax splice:sr -j anno.bed12 ref.fa r1.fq r2.fq > aln.sam ./minimap2 -cx asm5 asm1.fa asm2.fa > aln.paf # intra-species asm-to-asm alignment ./minimap2 -x ava-pb reads.fa reads.fa > overlaps.paf # PacBio read overlap ./minimap2 -x ava-ont reads.fa reads.fa > overlaps.paf # Nanopore read overlap

man page for detailed command line options

man ./minimap2.1 ```

Table of Contents

• Getting Started
• Users' Guide
  • Installation
  • General usage
  • Use cases
  • Map long noisy genomic reads
  • Map long mRNA/cDNA reads
  • Find overlaps between long reads
  • Map short genomic reads
  • Map short RNA-seq reads
  • Full genome/assembly alignment
  • Advanced features
  • Working with >65535 CIGAR operations
  • The cs optional tag
  • Working with the PAF format
  • Algorithm overview
  • Getting help
  • Citing minimap2
• Developers' Guide
• Limitations

Users' Guide

Minimap2 is a versatile sequence alignment program that aligns DNA or mRNA sequences against a large reference database. Typical use cases include: (1) mapping PacBio or Oxford Nanopore genomic reads to the human genome; (2) finding overlaps between long reads with error rate up to ~15%; (3) splice-aware alignment of PacBio Iso-Seq or Nanopore cDNA or Direct RNA reads against a reference genome; (4) aligning Illumina single- or paired-end reads; (5) assembly-to-assembly alignment; (6) full-genome alignment between two closely related species with divergence below ~15%.

For ~10kb noisy reads sequences, minimap2 is tens of times faster than mainstream long-read mappers such as BLASR, BWA-MEM, NGMLR and GMAP. It is more accurate on simulated long reads and produces biologically meaningful alignment ready for downstream analyses. For >100bp Illumina short reads, minimap2 is three times as fast as BWA-MEM and Bowtie2, and as accurate on simulated data. Detailed evaluations are available from the minimap2 paper or the preprint.

Installation

Minimap2 is optimized for x86-64 CPUs. You can acquire precompiled binaries from the release page with: sh curl -L https://github.com/lh3/minimap2/releases/download/v2.30/minimap2-2.30_x64-linux.tar.bz2 | tar -jxvf - ./minimap2-2.30_x64-linux/minimap2 If you want to compile from the source, you need to have a C compiler, GNU make and zlib development files installed. Then type make in the source code directory to compile. If you see compilation errors, try make sse2only=1 to disable SSE4 code, which will make minimap2 slightly slower.

Minimap2 also works with ARM CPUs supporting the NEON instruction sets. To compile for 32 bit ARM architectures (such as ARMv7), use make arm_neon=1. To compile for for 64 bit ARM architectures (such as ARMv8), use make arm_neon=1 aarch64=1.

Minimap2 can use SIMD Everywhere (SIMDe) library for porting implementation to the different SIMD instruction sets. To compile using SIMDe, use make -f Makefile.simde. To compile for ARM CPUs, use Makefile.simde with the ARM related command lines given above.

General usage

Without any options, minimap2 takes a reference database and a query sequence file as input and produce approximate mapping, without base-level alignment (i.e. coordinates are only approximate and no CIGAR in output), in the PAF format: sh minimap2 ref.fa query.fq > approx-mapping.paf You can ask minimap2 to generate CIGAR at the cg tag of PAF with: sh minimap2 -c ref.fa query.fq > alignment.paf or to output alignments in the SAM format: sh minimap2 -a ref.fa query.fq > alignment.sam Minimap2 seamlessly works with gzip'd FASTA and FASTQ formats as input. You don't need to convert between FASTA and FASTQ or decompress gzip'd files first.

For the human reference genome, minimap2 takes a few minutes to generate a minimizer index for the reference before mapping. To reduce indexing time, you can optionally save the index with option -d and replace the reference sequence file with the index file on the minimap2 command line: sh minimap2 -d ref.mmi ref.fa # indexing minimap2 -a ref.mmi reads.fq > alignment.sam # alignment Importantly, it should be noted that once you build the index, indexing parameters such as -k, -w, -H and -I can't be changed during mapping. If you are running minimap2 for different data types, you will probably need to keep multiple indexes generated with different parameters. This makes minimap2 different from BWA which always uses the same index regardless of query data types.

Use cases

Minimap2 uses the same base algorithm for all applications. However, due to the different data types it supports (e.g. short vs long reads; DNA vs mRNA reads), minimap2 needs to be tuned for optimal performance and accuracy. It is usually recommended to choose a preset with option -x, which sets multiple parameters at the same time. The default setting is the same as map-ont.

Map long noisy genomic reads

sh minimap2 -ax map-pb ref.fa pacbio-reads.fq > aln.sam # for PacBio CLR reads minimap2 -ax map-ont ref.fa ont-reads.fq > aln.sam # for Oxford Nanopore reads minimap2 -ax map-iclr ref.fa iclr-reads.fq > aln.sam # for Illumina Complete Long Reads The difference between map-pb and map-ont is that map-pb uses homopolymer-compressed (HPC) minimizers as seeds, while map-ont uses ordinary minimizers as seeds. Empirical evaluation suggests HPC minimizers improve performance and sensitivity when aligning PacBio CLR reads, but hurt when aligning Nanopore reads. map-iclr uses an adjusted alignment scoring matrix that accounts for the low overall error rate in the reads, with transversion errors being less frequent than transitions.

Map long mRNA/cDNA reads

sh minimap2 -ax splice:hq -uf ref.fa iso-seq.fq > aln.sam # PacBio Iso-seq/traditional cDNA minimap2 -ax splice ref.fa nanopore-cdna.fa > aln.sam # Nanopore 2D cDNA-seq minimap2 -ax splice -uf -k14 ref.fa direct-rna.fq > aln.sam # Nanopore Direct RNA-seq minimap2 -ax splice --splice-flank=no SIRV.fa SIRV-seq.fa # mapping against SIRV control There are different long-read RNA-seq technologies, including tranditional full-length cDNA, EST, PacBio Iso-seq, Nanopore 2D cDNA-seq and Direct RNA-seq. They produce data of varying quality and properties. By default, -x splice assumes the read orientation relative to the transcript strand is unknown. It tries two rounds of alignment to infer the orientation and write the strand to the ts SAM/PAF tag if possible. For Iso-seq, Direct RNA-seq and tranditional full-length cDNAs, it would be desired to apply -u f to force minimap2 to consider the forward transcript strand only. This speeds up alignment with slight improvement to accuracy. For noisy Nanopore Direct RNA-seq reads, it is recommended to use a smaller k-mer size for increased sensitivity to the first or the last exons.

Minimap2 rates an alignment by the score of the max-scoring sub-segment, excluding introns, and marks the best alignment as primary in SAM. When a spliced gene also has unspliced pseudogenes, minimap2 slightly prefers the spliced alignment. By default, minimap2 outputs up to five secondary alignments (i.e. likely pseudogenes in the context of RNA-seq mapping). This can be tuned with option -N.

For long RNA-seq reads, minimap2 may produce chimeric alignments potentially caused by gene fusions/structural variations or by an intron longer than the max intron length -G (200k by default). For now, it is not recommended to apply an excessively large -G as this slows down minimap2 and sometimes leads to false alignments.

It is worth noting that by default -x splice prefers GT[A/G]..[C/T]AG over GT[C/T]..[A/G]AG, and then over other splicing signals. Considering one additional base improves the junction accuracy for noisy reads, but reduces the accuracy when aligning against the widely used SIRV control data. This is because SIRV does not honor the evolutionarily conservative splicing signal. If you are studying SIRV, you may apply --splice-flank=no to let minimap2 only model GT..AG, ignoring the additional base.

Since v2.17, minimap2 can optionally take annotated genes as input and prioritize on annotated splice junctions. To use this feature, you can sh paftools.js gff2bed anno.gff > anno.bed minimap2 -ax splice --junc-bed anno.bed ref.fa query.fa > aln.sam Here, anno.gff is the gene annotation in the GTF or GFF3 format (gff2bed automatically tests the format). The output of gff2bed is in the 12-column BED format, or the BED12 format. With the --junc-bed option, minimap2 adds a bonus score (tuned by --junc-bonus) if an aligned junction matches a junction in the annotation. Option --junc-bed also takes 5-column BED, including the strand field. In this case, each line indicates an oriented junction.

Note: --junc-bed is intended for long noisy RNA-seq reads only. Applying the option to short RNA-seq reads would increase run time with little improvement to junction accuracy.

Find overlaps between long reads

sh minimap2 -x ava-pb reads.fq reads.fq > ovlp.paf # PacBio CLR read overlap minimap2 -x ava-ont reads.fq reads.fq > ovlp.paf # Oxford Nanopore read overlap Similarly, ava-pb uses HPC minimizers while ava-ont uses ordinary minimizers. It is usually not recommended to perform base-level alignment in the overlapping mode because it is slow and may produce false positive overlaps. However, if performance is not a concern, you may try to add -a or -c anyway.

Map short genomic reads

sh minimap2 -ax sr ref.fa reads-se.fq > aln.sam # single-end alignment minimap2 -ax sr ref.fa read1.fq read2.fq > aln.sam # paired-end alignment minimap2 -ax sr ref.fa reads-interleaved.fq > aln.sam # paired-end alignment When two read files are specified, minimap2 reads from each file in turn and merge them into an interleaved stream internally. Two reads are considered to be paired if they are adjacent in the input stream and have the same name (with the /[0-9] suffix trimmed if present). Single- and paired-end reads can be mixed.

Map short RNA-seq reads

```sh minimap2 -ax splice:sr ref.fa reads-se.fq.gz > aln.sam # single-end minimap2 -ax splice:sr ref.fa r1.fq.gz r2.fq.gz > aln.sam # paired-end minimap2 -ax splice:sr -j anno.bed ref.fa r1.fq r2.fq > aln.sam # use annotation

2-pass alignment

minimap2 -x splice:sr -j anno.bed --write-junc ref.fa r1.fq r2.fq > junc.bed minimap2 -ax splice:sr -j anno.bed --pass1=junc.bed ref.fa r1.fq r2.fq > aln.sam `` The new presetsplice:srwas added in v2.29. It functions similarly tosr` except that it performs spliced alignment.

Full genome/assembly alignment

sh minimap2 -ax asm5 ref.fa asm.fa > aln.sam # assembly to assembly/ref alignment For cross-species full-genome alignment, the scoring system needs to be tuned according to the sequence divergence.

Advanced features

Working with >65535 CIGAR operations

Due to a design flaw, BAM does not work with CIGAR strings with >65535 operations (SAM and CRAM work). However, for ultra-long nanopore reads minimap2 may align ~1% of read bases with long CIGARs beyond the capability of BAM. If you convert such SAM/CRAM to BAM, Picard and recent samtools will throw an error and abort. Older samtools and other tools may create corrupted BAM.

To avoid this issue, you can add option -L at the minimap2 command line. This option moves a long CIGAR to the CG tag and leaves a fully clipped CIGAR at the SAM CIGAR column. Current tools that don't read CIGAR (e.g. merging and sorting) still work with such BAM records; tools that read CIGAR will effectively ignore these records. It has been decided that future tools will seamlessly recognize long-cigar records generated by option -L.

TL;DR: if you work with ultra-long reads and use tools that only process BAM files, please add option -L.

The cs optional tag

The cs SAM/PAF tag encodes bases at mismatches and INDELs. It matches regular expression /(:[0-9]+|\*[a-z][a-z]|[=\+\-][A-Za-z]+)+/. Like CIGAR, cs consists of series of operations. Each leading character specifies the operation; the following sequence is the one involved in the operation.

The cs tag is enabled by command line option --cs. The following alignment, for example: txt CGATCGATAAATAGAGTAG---GAATAGCA |||||| |||||||||| |||| ||| CGATCG---AATAGAGTAGGTCGAATtGCA is represented as :6-ata:10+gtc:4*at:3, where :[0-9]+ represents an identical block, -ata represents a deletion, +gtc an insertion and *at indicates reference base a is substituted with a query base t. It is similar to the MD SAM tag but is standalone and easier to parse.

If --cs=long is used, the cs string also contains identical sequences in the alignment. The above example will become =CGATCG-ata=AATAGAGTAG+gtc=GAAT*at=GCA. The long form of cs encodes both reference and query sequences in one string. The cs tag also encodes intron positions and splicing signals (see the minimap2 manpage for details).

Working with the PAF format

Minimap2 also comes with a (java)script paftools.js that processes alignments in the PAF format. It calls variants from assembly-to-reference alignment, lifts over BED files based on alignment, converts between formats and provides utilities for various evaluations. For details, please see misc/README.md.

Algorithm overview

In the following, minimap2 command line options have a dash ahead and are highlighted in bold. The description may help to tune minimap2 parameters.

1. Read -I [=4G] reference bases, extract (-k,-w)-minimizers and index them in a hash table.

2. Read -K [=200M] query bases. For each query sequence, do step 3 through 7:

3. For each (-k,-w)-minimizer on the query, check against the reference index. If a reference minimizer is not among the top -f [=2e-4] most frequent, collect its the occurrences in the reference, which are called seeds.

4. Sort seeds by position in the reference. Chain them with dynamic programming. Each chain represents a potential mapping. For read overlapping, report all chains and then go to step 8. For reference mapping, do step 5 through 7:

5. Let P be the set of primary mappings, which is an empty set initially. For each chain from the best to the worst according to their chaining scores: if on the query, the chain overlaps with a chain in P by --mask-level [=0.5] or higher fraction of the shorter chain, mark the chain as secondary to the chain in P; otherwise, add the chain to P.

6. Retain all primary mappings. Also retain up to -N [=5] top secondary mappings if their chaining scores are higher than -p [=0.8] of their corresponding primary mappings.

7. If alignment is requested, filter out an internal seed if it potentially leads to both a long insertion and a long deletion. Extend from the left-most seed. Perform global alignments between internal seeds. Split the chain if the accumulative score along the global alignment drops by -z [=400], disregarding long gaps. Extend from the right-most seed. Output chains and their alignments.

8. If there are more query sequences in the input, go to step 2 until no more queries are left.

9. If there are more reference sequences, reopen the query file from the start and go to step 1; otherwise stop.

Getting help

Manpage minimap2.1 provides detailed description of minimap2 command line options and optional tags. The FAQ page answers several frequently asked questions. If you encounter bugs or have further questions or requests, you can raise an issue at the issue page. There is not a specific mailing list for the time being.

Citing minimap2

If you use minimap2 in your work, please cite:

Li, H. (2018). Minimap2: pairwise alignment for nucleotide sequences. Bioinformatics, 34:3094-3100. doi:10.1093/bioinformatics/bty191

and/or:

Li, H. (2021). New strategies to improve minimap2 alignment accuracy. Bioinformatics, 37:4572-4574. doi:10.1093/bioinformatics/btab705

Developers' Guide

Minimap2 is not only a command line tool, but also a programming library. It provides C APIs to build/load index and to align sequences against the index. File example.c demonstrates typical uses of C APIs. Header file minimap.h gives more detailed API documentation. Minimap2 aims to keep APIs in this header stable. File mmpriv.h contains additional private APIs which may be subjected to changes frequently.

This repository also provides Python bindings to a subset of C APIs. File python/README.rst gives the full documentation; python/minimap2.py shows an example. This Python extension, mappy, is also available from PyPI via pip install mappy or from BioConda via conda install -c bioconda mappy.

Limitations

• Minimap2 may produce suboptimal alignments through long low-complexity regions where seed positions may be suboptimal. This should not be a big concern because even the optimal alignment may be wrong in such regions.

• Minimap2 requires SSE2 instructions on x86 CPUs or NEON on ARM CPUs. It is possible to add non-SIMD support, but it would make minimap2 slower by several times.

• Minimap2 does not work with a single query or database sequence ~2 billion bases or longer (2,147,483,647 to be exact). The total length of all sequences can well exceed this threshold.

• Minimap2 often misses small exons.