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Project Description

pRESTO - The REpertoire Sequencing TOolkit

pRESTO is a toolkit for processing raw reads from high-throughput sequencing of lymphocyte repertoires.

Dramatic improvements in high-throughput sequencing technologies now enable large-scale characterization of immunoglobulin repertoires, defined as the collection of trans-membrane antigen-receptor proteins located on the surface of T and B lymphocytes. The REpertoire Sequencing TOolkit (pRESTO) is composed of a suite of utilities to handle all stages of sequence processing prior to germline segment assignment. pRESTO is designed to handle either single reads or paired-end reads. It includes features for quality control, primer masking, annotation of reads with sequence embedded barcodes, generation of unique molecular identifier (UMI) consensus sequences, assembly of paired-end reads and identification of duplicate sequences. Numerous options for sequence sorting, sampling and conversion operations are also included.

Installation

The latest stable release of pRESTO may be downloaded from PyPI or Bitbucket. The simplest way to install the latest stable release of pRESTO is via pip:

> pip3 install presto

Linux

  1. The simplest way to install all Python dependencies is to install the full SciPy stack using the instructions, then install Biopython according to its instructions.

  2. Download the pRESTO bundle and run:

    > pip3 install presto-x.y.z.tar.gz --user
    

Mac OS X

  1. Install Xcode. Available from the Apple store or developer downloads.

  2. Older versions Mac OS X will require you to install XQuartz 2.7.5. Available from the XQuartz project.

  3. Install Homebrew following the installation and post-installation instructions.

  4. Install Python 3.4.0+ and set the path to the python3 executable:

    > brew install python3
    > echo 'export PATH=/usr/local/bin:$PATH' >> ~/.profile
    
  5. Exit and reopen the terminal application so the PATH setting takes effect.

  6. You may, or may not, need to install gfortran (required for SciPy). Try without first, as this can take an hour to install and is not needed on newer releases. If you do need gfortran to install SciPy, you can install it using Homebrew:

    > brew install gfortran
    

    If the above fails run this instead:

    > brew install --env=std gfortran
    
  7. Install NumPy, SciPy, pandas and Biopyton using the Python package manager:

    > pip3 install numpy scipy pandas biopython
    
  8. Download the pRESTO bundle, open a terminal window, change directories to the download folder, and run:

    > pip3 install presto-x.y.z.tar.gz
    

Windows

  1. Install Python 3.4.0+ from Python, selecting both the options ‘pip’ and ‘Add python.exe to Path’.

  2. Install NumPy, SciPy, pandas and Biopython using the packages available from the Unofficial Windows binary collection.

  3. Download the pRESTO bundle, open a Command Prompt, change directories to the download folder, and run:

    > pip install presto-x.y.z.tar.gz
    
  4. For a default installation of Python 3.4, the pRESTO scripts will be installed into C:\Python34\Scripts and should be directly executable from the Command Prompt. If this is not the case, then follow step 5 below.

  5. Add both the C:\Python34 and C:\Python34\Scripts directories to your %Path%. On Windows 7 the %Path% setting is located under Control Panel -> System and Security -> System -> Advanced System Settings -> Environment variables -> System variables -> Path.

Release Notes

Version 0.5.2: March 8, 2016

Fixed a bug with installation on Windows due to old file paths lingering in presto.egg-info/SOURCES.txt.

Improvements to commandline usage help messages.

Updated license from CC BY-NC-SA 3.0 to CC BY-NC-SA 4.0.

AssemblePairs:

  • Added the flag --fill to the reference subcommand to allow insertion of the reference sequence into the non-overlapping region of assembled sequences. Use caution when using this flag, as this may lead to chimeric sequences.
  • Changed default --minlen to 8 in align subcommand.

Version 0.5.1: December 4, 2015

ClusterSets:

  • Fixed bug wherein --failed flag did not work.

Version 0.5.0: September 7, 2015

Conversion to a proper Python package which uses pip and setuptools for installation.

The package now requires Python 3.4. Python 2.7 is not longer supported.

The required dependency versions have been bumped to numpy 1.8, scipy 0.14, pandas 0.15, and biopython 1.65.

IgCore:

  • Divided IgCore functionality into the separate modules: Annotation, Commandline, Defaults, IO, Multiprocessing and Sequence.

Version 0.4.8: September 7, 2015

Added support for additional input FASTA (.fna, .fa), FASTQ (.fq) and tab-delimited (.tsv) file extensions.

ParseHeaders:

  • Fixed a bug in the rename subcommand wherein renaming to an existing field deleted the old annotation, but did not merge the renamed annotation into the existing field.
  • Added the copy subcommand which will copy annotations into new field names or merge the annotations of existing fields.
  • Added the --act argument to the copy and rename subcommands allowing collapse following the copy or rename operation.
  • Added a commandline check to ensure that the -f, -k and --act arguments contain the same number of fields for both the rename and copy subcommands.

Version 0.4.7: June 5, 2015

IgCore:

  • Modified scoring functions to permit asymmetrical scores for N and gap characters.

AssemblePairs:

  • Added support for SRA style coordinate information where the where the read number has been appended to the spot number.
  • Altered scoring so gap characters are counted as mismatches in the error rate and identity calculations.

BuildConsensus:

  • Altered scoring so gap characters are counted as mismatches in the diversity and error rate calculations.

ConvertHeaders:

  • Added support for SRA style sequence headers where the read number has been appended to the spot number; eg, output from fastq-dump -I --split-files file.sra.

ClusterSets:

  • Added missing OUTPUT console log field.
  • Changed --bf and --cf arguments to -f and -k, respectively.

MaskPrimers:

  • Altering scoring behavior for N characters such that Ns in the input sequence are always counted as a mismatch, while Ns in the primer sequence are counted as a match, with priority given to the input sequence score.
  • Added --gap argument to the align subcommand which allows users to specify the gap open and gap extension penalties for aligning primers. Note: gap penalties reduce the match count for purposes of calculating ERROR.

PairSeq:

  • Added support for SRA style coordinate information where the where the read number has been appended to the spot number.

Version 0.4.6: May 13, 2015

BuildConsensus:

  • Changed --maxmiss argument to --maxgap and altered the behavior to only perform deletion of positions based on gap characters (only “-” or “.” and not “N” characters).
  • Added an error rate (--maxerror) calculation based on mismatches from consensus. The --maxerror argument is mutually exclusive with the --maxdiv argument and provides similar functionality. However, the calculations are not equivalent, and --maxerror should be considerably faster than --maxdiv.
  • Added exclusion of positions from the error rate calculation that are deleted due to exceeding the --maxgap threshold .
  • Fixed misalignment of consensus sequence against input sequences when positions are deleted due to exceeding the --maxgap threshold.

ClusterSets:

  • New script to cluster read groups by barcode field (eg, UID barcodes) into clustering within the read group.

ConvertHeaders:

  • New script to handle conversion of different sequence description formats to the pRESTO format.

FilterSeq:

  • Added count of masked characters to log output of maskqual subcommand.
  • Changed repeats subcommand log field REPEAT to REPEATS.

PairSeq:

  • Changed -f argument to --1f argument.
  • Added --2f argument to copy file 2 annotations to file 1.

ParseHeaders:

  • Moved convert subcommand to the generic subcommand of the new ConvertHeaders script and modified the conversion behavior.

Version 0.4.5: March 20, 2015

Added details to the usage documentation for each tool which describes both the output files and annotation fields.

Renamed --clean argument to --failed argument with opposite behavior, such that the default behavior of all scripts is now clean output.

IgCore:

  • Features added for Change-O compatibility.
  • Features added for PairSeq performance improvements.
  • Added custom help formatter.
  • Modifications to internals of multiprocessing code.
  • Fixed a few typos in error messages.

AssemblePairs:

  • Added reference subcommand which uses V-region germline alignments from ublast to assemble paired-ends.
  • Removed mate-pair matching operation to increase performance. Now requires both input files to contain matched and uniformly ordered reads. If files are not synchronized then PairSeq must be run first. AssemblePairs will check that coordinate info matches and error if the files are not synchronized. Unpaired reads are no longer output.
  • Added support for cases where one mate pair is the subsequence of the other.
  • Added --scanrev argument to allow for head sequence to overhang end of tail.
  • Removed truncated (quick) error calculation in align subcommand.
  • Changed default values of the --maxerror and --alpha arguments of the align subcommand to better tuned parameters.
  • Changed internal selection of top scoring alignment to use Z-score approximation rather than a combination of error rate and binomial mid-p value.
  • Internal changes to multiprocessing structure.
  • Changed inserted gap character from - to N in join subcommand for better compatibility with the behavior of IMGT/HighV-QUEST.
  • Changed PVAL log field to PVALUE.
  • Changed HEADSEQ and TAILSEQ log fields to SEQ1 and SEQ2.
  • Changed HEADFIELDS and TAILFIELDS log fields to FIELDS1 and FIELDS2.
  • Changed precision of ERROR and PVALUE log fields.
  • Added more verbose logging.

BuildConsensus:

  • Fixed bug where low quality positions where not being masked in single sequence barcode groups.
  • Added copy field (--cf) and copy action (--act) arguments to generate consensus annotations for barcode read groups.
  • Changed maximum consensus quality score from 93 to 90.

CollapseSeq:

  • Added --keep argument to allow retention of sequences with high missing character counts in unique sequence output file.
  • Removed case insensitivity for performance reasons. Now requires all sequences to have matching case.
  • Removed first and last from --act choices to avoid unexpected behavior.

MaskPrimers:

  • Changed behavior of N characters in primer identification. Ns now count as a match against any character, rather than a mismatch.
  • Changed behavior of mask mode such that positions masked with Ns are now assigned quality scores of 0, rather than retaining their previous scores.
  • Fixed a bug with the align subcommand where deletions within the input sequence (gaps in the alignment) were causing an incorrect barcode start position.

PairSeq:

  • Performance improvements. The tool should now be considerably faster on very large files.
  • Specifying the --failed argument to request output of sequences which do not have a mate pair will increase run time and memory usage.

ParseHeaders:

  • Add ‘cat’ action to collapse subcommand which concatenates strings into a single annotation.

SplitSeq:

  • Removed --clean (and --failed) flag from all subcommands.
  • Added progress updates to sample and samplepair subcommands.
  • Performance improvements to samplepair subcommand.

Version 0.4.4: June 10, 2014

SplitSeq:

  • Removed a linux-specific dependency, allowing SplitSeq to work on Windows.

Version 0.4.3: April 7, 2014

CollapseSeq:

  • Fixed bug that occurs with Python 2.7.5 on OS X.

SplitSeq:

  • Fixed bug in samplepairs subcommand that occurs with Python 2.7.5 on OS X.

Version 0.4.2: March 20, 2014

Increased verbosity of exception reporting.

IgCore:

  • Updates to consensus functions to support changes to BuildConsensus.

AssemblePairs:

  • Set default alpha to 0.01.

BuildConsensus:

  • Added support for --freq value parameter to quality consensus method and set default value to 0.6.
  • Fixed a bug in the frequency consensus method where missing values were contributing to the total character count at each position.
  • Added the parameter --maxmiss value which provides a cut-off for removal of positions with too many N or gap characters .

MaskPrimers:

  • Renamed the --reverse parameter to --revpr.

SplitSeq:

  • Removed convert subcommand.

Version 0.4.1: January 27, 2014

Changes to the internals of multiple tools to provide support for multiprocessing in Windows environments.

Changes to the internals of multiple tools to provide clean exit of child processes upon kill signal or exception in sibling process.

Fixed unexpected behavior of --outname and --log arguments with multiple input files.

IgCore:

  • Added reporting of unknown exceptions when reading sequence files
  • Fixed scoring of lowercase sequences.

AlignSets:

  • Fixed a typo in the log output.

BuildConsensus:

  • Fixed a typo in the log output.

EstimateError:

  • Fixed bug where tool would improperly exit if no sets passed threshold criteria.
  • Fixed typo in console output.

MaskPrimers:

  • Added trim mode which will cut the region before primer alignment, but leave primer region unmodified.
  • Fixed a bug with lowercase sequence data.
  • Fixed bug in the console and log output.
  • Added support for primer matching when setting --maxerr 1.0.

ParseHeaders:

  • Added count of sequences without any valid fields (FAIL) to console output.

ParseLog:

  • Added count of records without any valid fields (FAIL) to console output.

SplitSeq:

  • Fixed typo in console output of samplepair subcommand.
  • Added increase of the open file limit to the group subcommand to allow for a large number of groups.

Version 0.4.0: September 30, 2013

Minor name changes were made to multiple scripts, functions, parameters, and output files.

AlignSets, AssemblePairs, BuildConsensus, EstimateError, FilterSeq, and MaskPrimers are now multithreaded. The number of simultaneous processes may be specified using --nproc value. Note this means file ordering is no longer preserved between the input and output sequence files.

Performance improvements were made to several tools.

The universal --verbose parameter was replaced with --log file_name which specifies a log file for verbose output, and disables verbose logging if not specified.

The report of input parameters and sequence counts is now separate from the log and is always printed to standard output.

Added a progress bar to the standard output of most tools.

Added a universal --outname file_prefix parameter which changes the leading portion of the output file name. If not specified, the current file name is used (excluding the file extension, as per the previous behavior).

Added a universal --clean parameter which if specified forces the tool not to create an output file of sequences which failed processing.

IgCore:

  • Changes to parameters and internals of multiple functions.
  • Added functions to support multithreading for single-end reads, paired-end reads, and barcode sets.
  • Added safe annotation field renaming.
  • Added progress bar, logging and output file name conversion support.
  • Moved reusable AssemblePairs, BuildConsensus, PairSeq, and SplitSeq. operations into IgCore.

AssemblePairs:

  • Coordinate information is now specified by a coordinate type, rather than a delimiter, using the --coord header_type parameter, where the header type may be one of illumina, solexa, sra, 454, presto.

CollapseSeq:

  • Sequences with a missing character count exceeding the user limit defined by -n maximum_missing_count are now exported to a separate collapse-undetermined output file, rather than included in the collapse-unique sequence output.

EstimateError:

  • Now outputs error estimations for positions, quality scores, nucleotide pairs, and annotation sets.
  • Machine reported quality scores and empirical quality scores have been added to all output tables.

FilterSeq:

  • Added length subcommand to filter sequences by minimum length.

PairSeq:

  • Coordinate information has been redefined as per AssemblePairs.

ParseHeaders:

  • Added new subcommand convert which attempts to reformat sequence headers into the pRESTO format.
  • The rename subcommand will now append entries if the new field name already exists in the sequence header, rather than replace the entry.

Version 0.3 (prerelease 6): August 13, 2013

Toolkit is now dependent upon pandas 0.12 for the estimateError tool.

alignSets:

  • Changed MUSCLE execution to faster settings (-diags, -maxiters 2).

filterQuality:

  • Added repeat subcommand to filter sequences with -n (value) repetitions of a single character and.
  • Changed -n parameter of ambig subcommand from fractional value to a raw count.

estimateError:

  • New tool which estimates error of sequence sets by comparison to a consensus.

maskPrimers:

  • Bug fixes to alignment position calculation of align subcommand when primer alignment begins before start of sequence.
  • Removed --ann parameter.

Version 0.3 (prerelease 5): August 7, 2013

License changed to Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License.

IgPipeline Core:

  • Bug fixes to diversity calculation.
  • Added support for files where all sequences do not share the same annotation fields.
  • Added support for alternate scoring of gap and N-valued nucleotides.

alignSets:

  • Added --mode parameter with options of pad and cut to specify whether to extend or trim read groups to the same start position.
  • Fixed intermittent ‘muscle’ subcommand stdout pipe deadlock when executing MUSCLE.

assemblePairs:

  • Added join subcommand to support library preps where paired-end reads do not overlap.
  • Speed improvements to p-value calculations.

buildConsensus:

  • --div parameter converted to --maxdiv value to allow filtering of read groups by diversity.
  • Bug fixes to nucleotide frequency consensus method.
  • -q parameter renamed to --qual.

collapseSequences:

  • Added support for files where all sequences do not share the same annotation fields.

splitSeqFile:

  • samplepair subcommand added to allow random sampling from paired-end file sets.
  • The behavior of the -c parameter of the sample and samplepair subcommands changed to allow multiple samplings with the same command.

Version 0.3 (prerelease 4): May 18, 2013

Initial public prerelease

Release History

Release History

0.5.2

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File Name & Checksum SHA256 Checksum Help Version File Type Upload Date
presto-0.5.2.tar.gz (85.2 kB) Copy SHA256 Checksum SHA256 Source Mar 8, 2016

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