pyfastx 0.4.1

pyfastx is a python module for fast random access to sequences from plain and gzipped FASTA/Q file

a robust python module for fast random access to sequences from plain and gzipped FASTA/Q file

Table of Contents

• Introduction

• Features

• Installation

• FASTA

  • Read FASTA file

  • Get FASTA information

  • Get longest and shortest sequence

  • Calculate N50 and L50

  • Get sequence mean and median length

  • Get sequence counts

  • Get subsequences

• Sequence

  • Get a sequence from FASTA

  • Get sequence information

  • Sequence slice

  • Reverse and complement sequence

  • Read sequence line by line

  • Search for subsequence

• FASTQ

  • Read FASTQ file

  • Get FASTQ information

• Read

  • Get read from FASTQ

  • Get read information

• Identifiers

• Testing

• Acknowledgements

Introduction

The pyfastx is a lightweight Python C extension that enables users to randomly access to sequences from plain and gzipped FASTA/Q files. This module aims to provide simple APIs for users to extract seqeunce from FASTA and reads from FASTQ by identifier and index number. The pyfastx will build indexes stored in a sqlite3 database file for random access to avoid consuming excessive amount of memory. In addition, the pyfastx can parse standard (sequence is spread into multiple lines with same length) and nonstandard (sequence is spread into one or more lines with different length) FASTA format. This module used kseq.h written by @attractivechaos in klib project to parse plain FASTA/Q file and zran.c written by @pauldmccarthy in project indexed_gzip to index gzipped file for random access.

This project was heavily inspired by @mdshw5’s project pyfaidx and @brentp’s project pyfasta.

Features

• Single file for the Python extension

• Lightweight, memory efficient for parsing FASTA file

• Fast random access to sequences from gzipped FASTA file

• Read sequences from FASTA file line by line

• Calculate assembly N50 and L50

• Calculate GC content and nucleotides composition

• Extract reverse, complement and antisense sequence

• Excellent compatibility, support for parsing nonstandard FASTA file

• Support for random access reads from FASTQ file

Installation

Make sure you have both pip and at least version 3.5 of Python before starting.

You can install pyfastx via the Python Package Index (PyPI)

pip install pyfastx

Update pyfastx module

pip install -U pyfastx

FASTA

Read FASTA file

The fastest way to parse flat or gzipped FASTA file without building index.

>>> import pyfastx
>>> for name, seq in pyfastx.Fasta('test/data/test.fa.gz', build_index=False):
>>>     print(name, seq)

Read flat or gzipped FASTA file and build index, support for random access to FASTA.

>>> import pyfastx
>>> fa = pyfastx.Fasta('test/data/test.fa.gz')
>>> fa
<Fasta> test/data/test.fa.gz contains 211 seqs

Note

Building index may take some times. The time required to build index depends on the size of FASTA file. If index built, you can randomly access to any sequences in FASTA file.

Get FASTA information

>>> # get sequence counts in FASTA
>>> len(fa)
211

>>> # get total sequence length of FASTA
>>> fa.size
86262

>>> # get GC content of DNA sequence of FASTA
>>> fa.gc_content
43.529014587402344

>>> # get GC skew of DNA sequences in FASTA
>>> # New in pyfastx 0.3.8
>>> fa.gc_skews
0.004287730902433395

>>> # get composition of nucleotides in FASTA
>>> fa.composition
{'A': 24534, 'C': 18694, 'G': 18855, 'T': 24179, 'N': 0}

Get longest and shortest sequence

New in pyfastx 0.3.0

>>> # get longest sequence (name, length)
>>> fa.longest
('JZ822609.1', 821)

>>> # get shortest sequence (name, length)
>>> fa.shortest
('JZ822617.1', 118)

Calculate N50 and L50

New in pyfastx 0.3.0

Calculate assembly N50 and L50, return (N50, L50), learn more about N50,L50

>>> # get FASTA N50 and L50
>>> fa.nl(50)
(516, 66)

>>> # get FASTA N90 and L90
>>> fa.nl(90)
(231, 161)

>>> # get FASTA N75 and L75
>>> fa.nl(75)
(365, 117)

Get sequence mean and median length

New in pyfastx 0.3.0

>>> # get sequence average length
>>> fa.mean
408

>>> # get seqeunce median length
>>> fa.median
430

Get sequence counts

New in pyfastx 0.3.0

Get counts of sequences whose length >= specified length

>>> # get counts of sequences with length >= 200 bp
>>> fa.count(200)
173

>>> # get counts of sequences with length >= 500 bp
>>> fa.count(500)
70

Get subsequences

Subseuqneces can be retrieved from FASTA file by using a list of [start, end] coordinates

>>> # get subsequence with start and end position
>>> interval = (1, 10)
>>> fa.fetch('JZ822577.1', interval)
'CTCTAGAGAT'

>>> # get subsequences with a list of start and end position
>>> intervals = [(1, 10), (50, 60)]
>>> fa.fetch('JZ822577.1', intervals)
'CTCTAGAGATTTTAGTTTGAC'

>>> # get subsequences with reverse strand
>>> fa.fetch('JZ822577.1', (1, 10), strand='-')
'ATCTCTAGAG'

Sequence

Get a sequence from FASTA

>>> # get sequence like a dictionary by identifier
>>> s1 = fa['JZ822577.1']
>>> s1
<Sequence> JZ822577.1 with length of 333

>>> # get sequence like a list by index
>>> s2 = fa[2]
>>> s2
<Sequence> JZ822579.1 with length of 176

>>> # get last sequence
>>> s3 = fa[-1]
>>> s3
<Sequence> JZ840318.1 with length of 134

>>> # check a sequence name weather in FASTA file
>>> 'JZ822577.1' in fa
True

Get sequence information

>>> s = fa[-1]
>>> s
<Sequence> JZ840318.1 with length of 134

>>> # get sequence order number in FASTA file
>>> # New in pyfastx 0.3.7
>>> s.id
211

>>> # get sequence name
>>> s.name
'JZ840318.1'

>>> # get sequence description
>>> # New in pyfastx 0.3.1
>>> s.description
'R283 cDNA library of flower petals in tree peony by suppression subtractive hybridization Paeonia suffruticosa cDNA, mRNA sequence'

>>> # get sequence string
>>> s.seq
'ACTGGAGGTTCTTCTTCCTGTGGAAAGTAACTTGTTTTGCCTTCACCTGCCTGTTCTTCACATCAACCTTGTTCCCACACAAAACAATGGGAATGTTCTCACACACCCTGCAGAGATCACGATGCCATGTTGGT'

>>> # get sequence length
>>> len(s)
134

>>> # get GC content if dna sequence
>>> s.gc_content
46.26865768432617

>>> # get nucleotide composition if dna sequence
>>> s.composition
{'A': 31, 'C': 37, 'G': 25, 'T': 41, 'N': 0}

Sequence slice

Sequence object can be sliced like a python string

>>> # get a sub seq from sequence
>>> s = fa[-1]
>>> ss = s[10:30]
>>> ss
<Sequence> JZ840318.1 from 11 to 30

>>> ss.name
'JZ840318.1:11-30'

>>> ss.seq
'CTTCTTCCTGTGGAAAGTAA'

>>> ss = s[-10:]
>>> ss
<Sequence> JZ840318.1 from 125 to 134

>>> ss.name
'JZ840318.1:125-134'

>>> ss.seq
'CCATGTTGGT'

Note

Slicing start and end coordinates are 0-based. Currently, pyfastx does not support an optional third step or stride argument. For example ss[::-1]

Reverse and complement sequence

>>> # get sliced sequence
>>> fa[0][10:20].seq
'GTCAATTTCC'

>>> # get reverse of sliced sequence
>>> fa[0][10:20].reverse
'CCTTTAACTG'

>>> # get complement of sliced sequence
>>> fa[0][10:20].complement
'CAGTTAAAGG'

>>> # get reversed complement sequence, corresponding to sequence in antisense strand
>>> fa[0][10:20].antisense
'GGAAATTGAC'

Read sequence line by line

New in pyfastx 0.3.0

The sequence object can be iterated line by line as they appear in FASTA file.

>>> for line in fa[0]:
...     print(line)
...
CTCTAGAGATTACTTCTTCACATTCCAGATCACTCAGGCTCTTTGTCATTTTAGTTTGACTAGGATATCG
AGTATTCAAGCTCATCGCTTTTGGTAATCTTTGCGGTGCATGCCTTTGCATGCTGTATTGCTGCTTCATC
ATCCCCTTTGACTTGTGTGGCGGTGGCAAGACATCCGAAGAGTTAAGCGATGCTTGTCTAGTCAATTTCC
CCATGTACAGAATCATTGTTGTCAATTGGTTGTTTCCTTGATGGTGAAGGGGCTTCAATACATGAGTTCC
AAACTAACATTTCTTGACTAACACTTGAGGAAGAAGGACAAGGGTCCCCATGT

Note

Sliced sequence (e.g. fa[0][10:50]) cannot be read line by line

Search for subsequence

New in pyfastx 0.3.6

Search for subsequence from given sequence and get one-based start position of the first occurrence

>>> # search subsequence in sense strand
>>> fa[0].search('GCTTCAATACA')
262

>>> # check subsequence weather in sequence
>>> 'GCTTCAATACA' in fa[0]
True

>>> # search subsequence in antisense strand
>>> fa[0].search('CCTCAAGT', '-')
301

FASTQ

New in pyfastx 0.4.0

Read FASTQ file

The fastest way to parse plain or gzipped FASTQ file without building index.

>>> import pyfastx
>>> for read in pyfastx.Fastq('tests/data/test.fq.gz', build_index=False):
>>>     print(read.name, read.seq, read.qual)

Read plain or gzipped file and build index, support for random access to reads from FASTQ.

>>> import pyfastx
>>> fq = pyfastx.Fastq('tests/data/test.fq.gz')
>>> fq
<Fastq> tests/data/test.fq.gz contains 100 reads

Get FASTQ information

>>> # get read counts in FASTQ
>>> len(fq)
800

>>> # get total bases
>>> fq.size
120000

>>> # get GC content of FASTQ file
>>> fq.gc_content
66.17471313476562

>>> # get composition of bases in FASTQ
>>> fq.composition
{'A': 20501, 'C': 39705, 'G': 39704, 'T': 20089, 'N': 1}

>>> # get phred which affects the quality score conversion
>>> fq.phred
33

>>> # Guess fastq quality encoding system
>>> # New in pyfastx 0.4.1
>>> fq.guess
['Sanger Phred+33', 'Illumina 1.8+ Phred+33']

Read

Get read from FASTQ

>>> #get read like a dict by read name
>>> r1 = fq['A00129:183:H77K2DMXX:1:1101:4752:1047']
>>> r1
<Read> A00129:183:H77K2DMXX:1:1101:4752:1047 with length of 150

>>> # get read like a list by index
>>> r2 = fq[10]
>>> r2
<Read> A00129:183:H77K2DMXX:1:1101:18041:1078 with length of 150

>>> # get the last read
>>> r3 = fq[-1]
>>> r3
<Read> A00129:183:H77K2DMXX:1:1101:31575:4726 with length of 150

>>> # check a read weather in FASTQ file
>>> 'A00129:183:H77K2DMXX:1:1101:4752:1047' in fq
True

Get read information

>>> r = fq[-10]
>>> r
<Read> A00129:183:H77K2DMXX:1:1101:1750:4711 with length of 150

>>> # get read order number in FASTQ file
>>> r.id
791

>>> # get read name
>>> r.name
'A00129:183:H77K2DMXX:1:1101:1750:4711'

>>> # get read length
>>> len(r)
150

>>> # get read sequence
>>> r.seq
'CGAGGAAATCGACGTCACCGATCTGGAAGCCCTGCGCGCCCATCTCAACCAGAAATGGGGTGGCCAGCGCGGCAAGCTGACCCTGCTGCCGTTCCTGGTCCGCGCCATGGTCGTGGCGCTGCGCGACTTCCCGCAGTTGAACGCGCGCTA'

>>> # get read quality ascii string
>>> r.qual
'FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FF,FFFFFFFFFFFFFFFFFFFFFFFFFF,F:FFFFFFFFF:'

>>> # get read quality integer value, ascii - 33 or 64
>>> r.quali
[37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 25, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 25, 37, 37, 11, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 37, 11, 37, 25, 37, 37, 37, 37, 37, 37, 37, 37, 37, 25]

>>> # get read length
>>> len(r)
150

Identifiers

Get all identifiers of sequence as a list-like object.

>>> ids = fa.keys()
>>> ids
<Identifier> contains 211 identifiers

>>> # get count of sequence
>>> len(ids)
211

>>> # get identifier by index
>>> ids[0]
'JZ822577.1'

>>> # check identifier where in fasta
>>> 'JZ822577.1' in ids
True

>>> # iter identifiers
>>> for name in ids:
>>>     print(name)

>>> # convert to a list
>>> list(ids)

Testing

The pyfaidx module was used to test pyfastx. To run the tests:

$ python setup.py test

Acknowledgements

kseq.h and zlib was used to parse FASTA format. Sqlite3 was used to store built indexes. pyfastx can randomly access to sequences from gzipped FASTA file mainly attributed to indexed_gzip.