Merge pull request #402 from ksahlin/release

Version 0.13.0

Author: marcelm

CHANGES.md

@@ -1,7 +1,11 @@
 # Strobealign Changelog
 
-## development version
+## v0.13.0 (2024-03-04)
 
+* #394: Added option `--aemb` (abundance estimation for metagenomic binning),
+  which makes strobealign output a table with estimated abundance values for
+  each contig (instead of SAM or PAF). This was contributed by Shaojun Pan
+  (@psj1997).
 * #386: Parallelize indexing even more by using @alugowski’s
   [poolSTL](https://github.com/alugowski/) `pluggable_sort`.
   Indexing a human reference (measured on CHM13) now takes only ~45 s on a

CMakeLists.txt

@@ -1,6 +1,6 @@
 cmake_minimum_required(VERSION 3.16)
 
-project(strobealign VERSION 0.12.0)
+project(strobealign VERSION 0.13.0)
 include(FetchContent)
 
 option(ENABLE_AVX "Enable AVX2 support" OFF)

CONTRIBUTING.md

@@ -24,7 +24,7 @@ If needed, run `make` with `VERBOSE=1` to get more logging output.
 After CMake has been run, you can use this one-liner to compile strobealign and
 run the tests:
 ```
-make -j -C build && tests/run.sh
+make -s -j -C build && tests/run.sh
 ```
 
 Whenever you make changes that could potentially affect mapping results, you can

README.md

@@ -77,47 +77,68 @@ as a developer.
 
 ### Python bindings
 
-Experimental and incomplete Python bindings can be installed with
+Experimental Python bindings can be installed with
 `pip install .`. The only documentation for the moment are the tests in
 `tests/*.py`.
 
 ## Usage
 
+To align paired-reads against a reference FASTA and produce a sorted BAM file,
+using eight threads:
 ```
-strobealign ref.fa reads.fq > output.sam                # Single-end reads
-strobealign ref.fa reads1.fq reads2.fq > output.sam     # Paired-end reads
-
-strobealign -x ref.fa reads.fq > output.paf             # Single-end reads mapping only (PAF)
-strobealign -x ref.fa reads1.fq reads2.fq > output.paf  # Paired-end reads mapping only (PAF)
+strobealign -t 8 ref.fa reads.1.fastq.gz reads.2.fastq.gz | samtools sort -o sorted.bam
 ```
 
-To use interleaved files, use the `--interleaved` flag:
-
+For single-end reads:
 ```
-strobealign ref.fa reads.fq --interleaved > output.sam  # Single and/or paired-end reads
+strobealign -t 8 ref.fa reads.fastq.gz | samtools sort -o sorted.bam
 ```
 
-To report secondary alignments, set parameter `-N [INT]` for a maximum of `[INT]` secondary alignments.
-
-The above commands are suitable for interactive use and test runs.
-For normal use, avoid creating SAM files on disk as they get very large compared
-to their compressed BAM counterparts. Instead, either pipe strobealign’s output
-into `samtools view` to create unsorted BAM files:
+For mixed reads (the input file can contain both single and paired-end reads):
 ```
-strobealign ref.fa reads.1.fastq.gz reads.2.fastq.gz | samtools view -o mapped.bam
+strobealign -t 8 ref.fa --interleaved reads.fastq.gz | samtools sort -o sorted.bam
 ```
-Or use `samtools sort` to create a sorted BAM file:
+
+In alignment mode, strobealign produces SAM output. By piping the output
+directly into `samtools`, the above commands avoid creating potentially large
+intermediate SAM files and also reduce disk I/O.
+
+To produce unsorted BAM, use `samtools view` instead of `samtools sort`.
+
+
+### Mapping-only mode
+
+The command-line option `-x` switches strobealign into mapping-only mode,
+in which it will output [PAF](https://github.com/lh3/miniasm/blob/master/PAF.md)
+files instead of SAM. For example:
 ```
-strobealign ref.fa reads.1.fastq.gz reads.2.fastq.gz | samtools sort -o sorted.bam
+strobealign -x -t 8 ref.fa reads.1.fastq.gz reads.2.fastq.gz | igzip > output.paf.gz
 ```
-This is usually faster than doing the two steps separately because fewer
-intermediate files are created.
+`igzip` is a faster version of gzip that is part of
+[ISA-L](https://github.com/intel/isa-l/).
+If it is not available, replace it with `pigz` or regular `gzip` in the
+command.
+
+
+## Abundance estimation mode (for metagenomic binning)
+
+The command-line option `--aemb` switches strobealign into abundance estimation
+mode, intended for metagenomic binning.
+In this mode, strobealign outputs a single table with abundance values in
+tab-separated value format instead of SAM or PAF.
 
-To output the estimated abundance of every contig, the format of output file is: contig_id \t abundance_value:
+Paired-end example:
 ```
-strobealign ref.fa reads.fq --aemb > abundance.txt                # Single-end reads
-strobealign ref.fa reads1.fq reads2.fq --aemb > abundance.txt     # Paired-end reads
+strobealign -t 8 --aemb ref.fa reads.1.fastq.gz reads.2.fastq.gz > abundances.tsv
 ```
+The output table contains one row for each contig of the reference.
+The first column is the reference/contig id and the second its abundance.
+
+The abundance is the number of bases mapped to a contig, divided by the length
+of the contig. Reads mapping to *n* different locations are weighted 1/*n*.
+
+Further columns may be added to this table in future versions of strobealign.
+
 
 ## Command-line options
 
@@ -127,12 +148,11 @@ options. Some important ones are:
 * `-r`: Mean read length. If given, this overrides the read length estimated
   from the input file(s). This is usually only required in combination with
   `--create-index`, see [index files](#index-files).
-* `-t N`, `--threads=N`: Use N threads. This mainly applies to the mapping step
-  as the indexing step is only partially parallelized.
+* `-t N`, `--threads=N`: Use N threads (both for mapping and indexing).
 * `--eqx`: Emit `=` and `X` CIGAR operations instead of `M`.
 * `-x`: Only map reads, do not do no base-level alignment. This switches the
   output format from SAM to [PAF](https://github.com/lh3/miniasm/blob/master/PAF.md).
-* `--aemb`: Output the estimated abundance value of every contig, the format of output file is: contig_id \t abundance_value.
+* `--aemb`: Output estimated abundance value of each contig, see section above.
 * `--rg-id=ID`: Add RG tag to each SAM record.
 * `--rg=TAG:VALUE`: Add read group metadata to the SAM header. This can be
   specified multiple times. Example: `--rg-id=1 --rg=SM:mysamle --rg=LB:mylibrary`.
@@ -172,19 +192,19 @@ To create an index, use the `--create-index` option.
 Since strobealign needs to know the read length, either provide it with
 read file(s) as if you wanted to map them:
 
-    strobealign --create-index ref.fa reads.1.fastq.gz reads.2.fastq.gz
+    strobealign --create-index -t 8 ref.fa reads.1.fastq.gz reads.2.fastq.gz
 
 Or set the read length explicitly with `-r`:
 
-    strobealign --create-index ref.fa -r 150
+    strobealign --create-index -t 8 ref.fa -r 150
 
 This creates a file named `ref.fa.rX.sti` containing the strobemer index,
 where `X` is the canonical read length that the index is optimized for (see
 above).
 To use the index when mapping, provide option `--use-index` when doing the
 actual mapping:
 
-    strobealign --use-index ref.fa reads.1.fastq.gz reads.2.fastq.gz | samtools ...
+    strobealign --use-index -t 8 ref.fa reads.1.fastq.gz reads.2.fastq.gz | samtools ...
 
 - Note that the `.sti` files are usually tied to a specific strobealign version.
   That is, when upgrading strobealign, the `.sti` files need to be regenerated.

setup.py

@@ -5,7 +5,7 @@
     name="strobealign",
     description="Python bindings for strobealign",
     license="MIT",
-    version="0.12.0",
+    version="0.13.0",
     packages=["strobealign"],
     package_dir={"": "src/python"},
     cmake_install_dir="src/python",