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SPRING

Build Status

SPRING is a compression tool for Fastq files (containing up to 4.29 Billion reads):

  • Near-optimal compression ratios for single-end and paired-end datasets
  • Fast and memory-efficient decompression
  • Supports variable length short reads of length upto 511 bases (without -l flag)
  • Supports variable length long reads of arbitrary length (upto 4.29 Billion) (with -l flag). This mode directly applies general purpose compression (BSC) to reads and so compression gains might be lower than those without -l flag.
  • Supports lossless compression of reads, quality scores and read identifiers
  • Supports reordering of reads (while preserving read pairing information) to boost compression
  • Supports quantization of quality values using QVZ, Illumina 8-level binning and binary thresholding
  • Supports decompression of a subset of reads (random access)
  • Supports gzipped fastq files as input (output) during (de)compression
  • Tested on Linux and macOS

Note: If you want to use SPRING only as a tool for reordering reads (approximately according to genome position), take a look at the reorder-only branch.

Install with conda on Linux

To install directly from source or to install on OSX, follow the instructions in the next section.

Spring is now available on conda via the bioconda channel. See this page for installation instructions for conda. Once conda is installed, do the following to install spring.

conda config --add channels defaults
conda config --add channels bioconda
conda config --add channels conda-forge
conda install spring

Note that if spring is installed this way, it should be invoked with the command spring rather than ./spring. The bioconda help page shows the commands if you wish to install spring in an environment.

Download

git clone https://github.com/shubhamchandak94/SPRING.git

Install

The instructions below will create the spring executable in the build directory inside SPRING. If you plan to build and run SPRING on separate architectures, then you might need to remove/comment the line set(FLAGS "${FLAGS} -march=native") in CMakeLists.txt (or use flags based on the target architecture).

On Linux with cmake installed and version at least 3.9 (check using cmake --version):

cd SPRING
mkdir build
cd build
cmake ..
make

On Linux with cmake not installed or with version older than 3.9:

cd SPRING
mkdir build
cd build
wget https://cmake.org/files/v3.10/cmake-3.10.3.tar.gz
tar -xzf cmake-3.10.3.tar.gz
cd cmake-3.10.3
./configure
make
cd ..
./cmake-3.10.3/bin/cmake ..
make

On macOS, install GCC compiler since Clang has issues with OpenMP library:

  • Install HomeBrew (https://brew.sh/)
  • Install GCC (this step will be faster if Xcode command line tools are already installed using xcode-select --install):
brew update
brew install gcc@9
  • Set environment variables:
export CC=gcc-9
export CXX=g++-9
  • Delete CMakeCache.txt (if present) from the build directory
  • Follow the steps above for Linux

Usage

Run the spring executable /PATH/TO/spring (or just spring if installed with conda) with the options below:

Allowed options:
  -h [ --help ]                   produce help message
  -c [ --compress ]               compress
  -d [ --decompress ]             decompress
  --decompress-range arg          --decompress-range start end
                                  (optional) decompress only reads (or read
                                  pairs for PE datasets) from start to end
                                  (both inclusive) (1 <= start <= end <=
                                  num_reads (or num_read_pairs for PE)). If -r
                                  was specified during compression, the range
                                  of reads does not correspond to the original
                                  order of reads in the FASTQ file.
  -i [ --input-file ] arg         input file name (two files for paired end)
  -o [ --output-file ] arg        output file name (for paired end
                                  decompression, if only one file is specified,
                                  two output files will be created by suffixing
                                  .1 and .2.)
  -w [ --working-dir ] arg (=.)   directory to create temporary files (default
                                  current directory)
  -t [ --num-threads ] arg (=8)   number of threads (default 8)
  -r [ --allow-read-reordering ]  do not retain read order during compression
                                  (paired reads still remain paired)
  --no-quality                    do not retain quality values during
                                  compression
  --no-ids                        do not retain read identifiers during
                                  compression
  -q [ --quality-opts ] arg       quality mode: possible modes are
                                  1. -q lossless (default)
                                  2. -q qvz qv_ratio (QVZ lossy compression,
                                  parameter qv_ratio roughly corresponds to
                                  bits used per quality value)
                                  3. -q ill_bin (Illumina 8-level binning)
                                  4. -q binary thr high low (binary (2-level)
                                  thresholding, quality binned to high if >=
                                  thr and to low if < thr)
  -l [ --long ]                   Use for compression of arbitrarily long read
                                  lengths. Can also provide better compression
                                  for reads with significant number of indels.
                                  -r disabled in this mode. For Illumina short
                                  reads, compression is better without -l flag.
  -g [ --gzipped_fastq ]          enable if compression input is gzipped fastq
                                  or to output gzipped fastq during
                                  decompression
  --fasta-input                   enable if compression input is fasta file
                                  (i.e., no qualities)                                

Note that the SPRING compressed files are tar archives consisting of the different compressed streams, although we recommend using the .spring extension as in the examples shown below.

Resource usage

For the memory and CPU performance for SPRING, please see the paper and the associated supplementary material. Note that SPRING uses some temporary disk space, and can fail if the disk space is not sufficient. Assuming that qualities and ids are not being discarded and SPRING is operating in the short read mode, the additional temporary disk usage is around 10-30% of the original uncompressed file (on the lower end when quality values are from newer Illumina machines and are more compressible) when -r flag is not specified (i.e., default lossless mode). When -r flag is specified, SPRING writes all the quality values and read ids to a temporary file leading to significantly higher temporary disk usage - closer to 70-80% of the original file size. Note that these figures are approximate and include the space needed for the final compressed file.

Example Usage of SPRING

This section contains several examples for SPRING compression and decompression with various modes and options. The compressed SPRING file uses the .spring extension as a convention. If installed using conda, use the command spring instead of ./spring.

For compressing file_1.fastq and file_2.fastq losslessly using default 8 threads (Lossless).

./spring -c -i file_1.fastq file_2.fastq -o file.spring

For compressing file_1.fastq.gz and file_2.fastq.gz (gzipped fastq files) losslessly using default 8 threads (Lossless).

./spring -c -i file_1.fastq.gz file_2.fastq.gz -o file.spring -g

Using 16 threads (Lossless).

./spring -c -i file_1.fastq file_2.fastq -o file.spring -t 16

Compressing with only paired end info preserved, ids not stored, qualities compressed after Illumina binning (Recommended lossy mode for older Illumina machines. For Novaseq files, lossless quality compression is recommmended).

./spring -c -i file_1.fastq file_2.fastq -r --no-ids -q ill_bin -o file.spring

Compressing with only paired end info preserved, ids not stored, qualities binary thresholded (qv < 20 binned to 6 and qv >= 20 binned to 40).

./spring -c -i file_1.fastq file_2.fastq -r --no-ids -q binary 20 40 6 -o file.spring

Compressing with only paired end info preserved, ids not stored, qualities quantized using qvz with approximately 1 bit used per quality value.

./spring -c -i file_1.fastq file_2.fastq -r --no-ids -q qvz 1.0 -o file.spring

Compressing only reads and ids.

./spring -c -i file_1.fastq file_2.fastq --no-quality -o file.spring

Compressing single-end long read Fastq losslessly.

./spring -c -l -i file.fastq  -o file.spring

For single end file, compressing without order preserved.

./spring -c -i file.fastq -r -o file.spring

For single end file, compressing with order preserved (lossless).

./spring -c -i file.fastq -o file.spring

Decompressing (single end) to file.fastq.

./spring -d -i file.spring -o file.fastq

Decompressing (single end) to file.fastq, only decompress reads from 400 to 10000000.

./spring -d -i file.spring -o file.fastq --decompress-range 400 1000000

Decompressing (paired end) to file.fastq.1 and file.fastq.2.

./spring -d -i file.spring -o file.fastq

Decompressing (paired end) to file_1.fastq and file_2.fastq.

./spring -d -i file.spring -o file_1.fastq file_2.fastq

Decompressing (paired end) to file_1.fastq.gz and file_2.fastq.gz.

./spring -d -i file.spring -o file_1.fastq.gz file_2.fastq.gz -g

Decompressing (paired end) to file_1.fastq and file_2.fastq, only decompress pairs from 4000000 to 8000000.

./spring -d -i file.spring -o file_1.fastq file_2.fastq --decompress-range 4000000 8000000

Compressing file_1.fasta and file_2.fasta (fasta files without qualities) losslessly using default 8 threads (Lossless).

./spring -c -i file_1.fasta file_2.fasta -o file.spring --fasta-input

Compressing (paired end) to file_1.fasta and file_2.fasta (previous example contd.).

./spring -d -i file.spring -o file_1.fasta file_2.fasta

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