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Releases: cbg-ethz/V-pipe

V-pipe 3.0 - prerelease 1

10 Jun 17:56
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Peer-review for publication

V-pipe 3.0 - prerelease 0

14 Oct 13:27
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Prerelease for publication.

2.99.3 Primers

02 Nov 16:03
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New features:

  • primer trimming using iVar (by default) or samtools

  • per sample primer protocol using new 4-column sample.tsv format (e.g.: for long running projects where protocols change to adapt to new variants)

    see: config/README.md#amplicon-protocols

  • frameshift_deletions_checks: report on stop codons

Bug fixes:

  • correctly compute runtime requirement within groups

Preview feature:

Documentation:

  • Improved tutorial available inside subdirectory docs/

⚠️ Breaking changes:

  • V-pipe now relies on snakemake 7.11 to properly handle 'runtime' resource. Consider upgrading !
  • by default the samples' tables coverage.tsv.gz and basecnt.tsv.gz are now 1-based: the first position of the genome is named '1' (as standard with genome notations, as in tools like samtools, and as used in formats like VCF)
    This can be switched back to 0-based (numbering starts at 0, as in python tools like PySAM, and as in the BED format) in config file, in section general option tsvbased

2.99.2 - Reports and uploads

30 Mar 16:18
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New features:

  • Mass-importer tools to assist building samples/ directory structure from .fastq.gz files.
    (see: utils/README.md)

  • Dehuman: V-pipe can now generate compressed .cram files from the raw reads that have been depleted from host (human) reads to assist upload to public databases such as, e.g, SRA.
    (see config manual, sections "output" and "dehuman")

  • Diversity: Computation of various diversity indices for the underlying samples following the review:
    doi:10.1016/j.coviro.2021.06.002
    (see config manual, sections "output" and "diversity")

Bugfixes:

  • frameshift_deletions_checks: English language reports now correctly covers insertions.

Preview features:

  • a series of tools and features that can be customized to assist in uploading results and raw reads to public databases such as ENA.
    (see config manual, sections "output" and "upload",
    see: workflow/scripts/prepare_upload_symlinks.sh)

2.99.1 Standardized usage

14 Oct 11:24
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New features

For legacy V-pipe 1.x/2.x users:

  • the new directory structure requires adapting old INI files
    please refer to config/README.md

NOTE:

  • currently only the analysis of NGS viral data is fully tested and
    guaranteed stable.
  • For other more advanced functionality (e.g., benchmarking) you might
    want to wait until a future release.

Toward a new gen V-pipe

14 Oct 10:39
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New features

This release incorporate numerous upgrades:

  • Visualisation
  • frameshift_deletions_checks
  • sample consensus fasta generated by bcftools
  • predicthaplo as an additional global haplotype engine
  • support for extremely large cohorts
    (e.g., stats computed per-sample and merged, instead of all BAMs)
  • snakemake resources
  • Automatic testing
  • Automatic Docker generation
  • Snakemake standard JSON/YAML configuration
  • virus_base_config instead of separate branches (like 'sars-cov2')

Legacy users

This is the last version that:

  • uses a working directory structure that is still similar to…
  • and can directly import configurations verbatim from…

…legacy versions of V-pipe 1.x/2.x and virus-branches (sars-cov2)

Working functionnality

  • currently only the analysis of NGS viral data is fully tested and
    guaranteed stable.
  • For other more advanced functionality (e.g., benchmarking) you might
    want to wait until a future release.

V-pipe 2.0: Benchmark functionalities

05 Jun 16:35
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  • simBench and testBench modules added to simulated reads from virus populations and evaluate read alignment bias and SNV calls, respectively
  • vpipeBench allows automated execution of the benchmark, from the generation of the in silico virus population to the evaluation of SNV calls
  • vpipeBenchRunner enables simultaneous execution of multiple pipeline configurations

This version of V-pipe was used to run computations reported in Posada-Céspedes et al (doi:10.1101/2020.06.09.142919)

NOTE: During the Gibbs sampling performed by ShoRAH, several clusters may generate the same haplotype representative. Such collisions result in inflated posterior values. Also, the averaging of the haplotype abundances across iterations can be affected by floating-point precision problems. Fortunately, ShoRAH also reports the number of reads assigned to each haplotype per iteration which we use to correct the aforementioned quantities in post-processing. We are currently implementing the changes required to resolve these issues in future releases of ShoRAH.

V-pipe 1.0

05 Jun 16:13
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  • Downgrade LoFreq version to 2.1.3 due to a reported issue (CSB5/lofreq#89) and build the reference sequence index as a separate rule
  • To build consensus sequences, report ambiguous base (N) when coverage is below 2 reads
  • Generalize module to detect flow-cell cross-contamimation
  • Basic report on number of reads after QC and alignment
  • Allow to call SNVs with respect to a reference sequence, instead of the consensus sequences built from all data sets analysed within a single run of the pipeline

V-pipe 1.0 release candidate

13 Apr 14:28
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This is a release candidate of Vpipe 1.0.

  • It has been tested on linux and macOS, using python 3.8 and snakemake 5.14.0. There are known limitations with executing SAVAGE for haplotype reconstruction on macOS.

  • Apart from VICUNA, all dependencies are managed by conda, and we strongly recommend to use --use-conda. VICUNA is only needed when reads are aligned with ngshmmalign and a references/initial_consensus.fasta file is not provided.

V-pipe pre-release

06 Apr 13:57
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V-pipe pre-release Pre-release
Pre-release

Changes:

  • Split rules into separate files to modularize pipeline code