minimap2 0.2.23.0 → 0.2.23.1

data/ext/minimap2/README.md

@@ -0,0 +1,403 @@
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+[![Build Status](https://github.com/lh3/minimap2/actions/workflows/ci.yaml/badge.svg)](https://github.com/lh3/minimap2/actions)
+## <a name="started"></a>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 or later)
+./minimap2 -ax asm20 ref.fa pacbio-ccs.fq.gz > aln.sam    # PacBio HiFi/CCS genomic reads (v2.18 or earlier)
+./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    # Final PacBio Iso-seq or traditional cDNA
+./minimap2 -ax splice --junc-bed anno.bed12 ref.fa query.fa > aln.sam  # prioritize on annotated junctions
+./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](#started)
+- [Users' Guide](#uguide)
+  - [Installation](#install)
+  - [General usage](#general)
+  - [Use cases](#cases)
+    - [Map long noisy genomic reads](#map-long-genomic)
+    - [Map long mRNA/cDNA reads](#map-long-splice)
+    - [Find overlaps between long reads](#long-overlap)
+    - [Map short accurate genomic reads](#short-genomic)
+    - [Full genome/assembly alignment](#full-genome)
+  - [Advanced features](#advanced)
+    - [Working with >65535 CIGAR operations](#long-cigar)
+    - [The cs optional tag](#cs)
+    - [Working with the PAF format](#paftools)
+  - [Algorithm overview](#algo)
+  - [Getting help](#help)
+  - [Citing minimap2](#cite)
+- [Developers' Guide](#dguide)
+- [Limitations](#limit)
+
+## <a name="uguide"></a>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][doi] or the
+[preprint][preprint].
+
+### <a name="install"></a>Installation
+
+Minimap2 is optimized for x86-64 CPUs. You can acquire precompiled binaries from
+the [release page][release] with:
+```sh
+curl -L https://github.com/lh3/minimap2/releases/download/v2.23/minimap2-2.23_x64-linux.tar.bz2 | tar -jxvf -
+./minimap2-2.23_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)][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.
+
+### <a name="general"></a>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][paf]:
+```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][sam]:
+```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.
+
+### <a name="cases"></a>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`.
+
+#### <a name="map-long-genomic"></a>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
+```
+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. Emperical evaluation suggests HPC minimizers improve
+performance and sensitivity when aligning PacBio CLR reads, but hurt when aligning
+Nanopore reads.
+
+#### <a name="map-long-splice"></a>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 does not intentionally
+prefer spliced alignment, though in practice it more often marks the spliced
+alignment as the primary. 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.
+
+#### <a name="long-overlap"></a>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.
+
+#### <a name="short-genomic"></a>Map short accurate 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.
+
+Minimap2 does not work well with short spliced reads. There are many capable
+RNA-seq mappers for short reads.
+
+#### <a name="full-genome"></a>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.
+
+### <a name="advanced"></a>Advanced features
+
+#### <a name="long-cigar"></a>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`.
+
+#### <a name="cs"></a>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][manpage-cs] for
+details).
+
+#### <a name="paftools"></a>Working with the PAF format
+
+Minimap2 also comes with a (java)script [paftools.js](misc/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](misc/README.md).
+
+### <a name="algo"></a>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.
+
+### <a name="help"></a>Getting help
+
+Manpage [minimap2.1][manpage] provides detailed description of minimap2
+command line options and optional tags. The [FAQ](FAQ.md) 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][issue].  There is not a
+specific mailing list for the time being.
+
+### <a name="cite"></a>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][doi]
+
+## <a name="dguide"></a>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](example.c) demonstrates typical uses of C APIs. Header
+file [minimap.h](minimap.h) gives more detailed API documentation. Minimap2
+aims to keep APIs in this header stable. File [mmpriv.h](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](python/README.rst) gives the full documentation;
+[python/minimap2.py](python/minimap2.py) shows an example. This Python
+extension, mappy, is also [available from PyPI][mappypypi] via `pip install
+mappy` or [from BioConda][mappyconda] via `conda install -c bioconda mappy`.
+
+## <a name="limit"></a>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.
+
+
+
+[paf]: https://github.com/lh3/miniasm/blob/master/PAF.md
+[sam]: https://samtools.github.io/hts-specs/SAMv1.pdf
+[minimap]: https://github.com/lh3/minimap
+[smartdenovo]: https://github.com/ruanjue/smartdenovo
+[longislnd]: https://www.ncbi.nlm.nih.gov/pubmed/27667791
+[gaba]: https://github.com/ocxtal/libgaba
+[ksw2]: https://github.com/lh3/ksw2
+[preprint]: https://arxiv.org/abs/1708.01492
+[release]: https://github.com/lh3/minimap2/releases
+[mappypypi]: https://pypi.python.org/pypi/mappy
+[mappyconda]: https://anaconda.org/bioconda/mappy
+[issue]: https://github.com/lh3/minimap2/issues
+[k8]: https://github.com/attractivechaos/k8
+[manpage]: https://lh3.github.io/minimap2/minimap2.html
+[manpage-cs]: https://lh3.github.io/minimap2/minimap2.html#10
+[doi]: https://doi.org/10.1093/bioinformatics/bty191
+[smide]: https://github.com/nemequ/simde
+[unimap]: https://github.com/lh3/unimap