artfastqgenerator 0.0.20150519-5 source package in Ubuntu

Changelog

artfastqgenerator (0.0.20150519-5) unstable; urgency=medium

  * Enable build with default Java 21
    Closes: #1053009
  * Enable build twice in a row
    Closes: #1043960
  * Standards-Version: 4.6.2 (routine-update)
  * Apply multi-arch hints.
     + artfastqgenerator-doc, artfastqgenerator-examples: Add Multi-Arch:
       foreign.
  * Lintian-overrides (see lintian bug #1017966)

 -- Andreas Tille <email address hidden>  Fri, 29 Sep 2023 14:28:38 +0200

Upload details

Uploaded by:
Debian Med
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
all
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Oracular release universe misc
Noble release universe misc

Builds

Noble: [FULLYBUILT] amd64

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artfastqgenerator_0.0.20150519-5.dsc 2.2 KiB bbf6d046fc64e47ad36de7057375d597ab10e5cdc38efa0276fa8e7175b075ec
artfastqgenerator_0.0.20150519.orig.tar.xz 1.1 MiB cbc41b9bf4f702c56fdec089482a9fd1cc606aeae91666f8d10569fdb23a53eb
artfastqgenerator_0.0.20150519-5.debian.tar.xz 6.3 KiB cd3905694ce164d44b1315266778fdcc399f2a97222ced5be9dd73de5c81b8e3

Available diffs

No changes file available.

Binary packages built by this source

artfastqgenerator: outputs artificial FASTQ files derived from a reference genome

 ArtificialFastqGenerator takes the reference genome (in FASTA format) as
 input and outputs artificial FASTQ files in the Sanger format. It can
 accept Phred base quality scores from existing FASTQ files, and use them
 to simulate sequencing errors. Since the artificial FASTQs are derived
 from the reference genome, the reference genome provides a gold-standard
 for calling variants (Single Nucleotide Polymorphisms (SNPs) and
 insertions and deletions (indels)). This enables evaluation of a Next
 Generation Sequencing (NGS) analysis pipeline which aligns reads to the
 reference genome and then calls the variants.

artfastqgenerator-doc: outputs artificial FASTQ files derived from a reference genome (doc)

 ArtificialFastqGenerator takes the reference genome (in FASTA format) as
 input and outputs artificial FASTQ files in the Sanger format. It can
 accept Phred base quality scores from existing FASTQ files, and use them
 to simulate sequencing errors. Since the artificial FASTQs are derived
 from the reference genome, the reference genome provides a gold-standard
 for calling variants (Single Nucleotide Polymorphisms (SNPs) and
 insertions and deletions (indels)). This enables evaluation of a Next
 Generation Sequencing (NGS) analysis pipeline which aligns reads to the
 reference genome and then calls the variants.
 .
 This package contains the Java API documentation for artfastqgenerator.

artfastqgenerator-examples: outputs artificial FASTQ files derived from a reference genome (examples)

 ArtificialFastqGenerator takes the reference genome (in FASTA format) as
 input and outputs artificial FASTQ files in the Sanger format. It can
 accept Phred base quality scores from existing FASTQ files, and use them
 to simulate sequencing errors. Since the artificial FASTQs are derived
 from the reference genome, the reference genome provides a gold-standard
 for calling variants (Single Nucleotide Polymorphisms (SNPs) and
 insertions and deletions (indels)). This enables evaluation of a Next
 Generation Sequencing (NGS) analysis pipeline which aligns reads to the
 reference genome and then calls the variants.
 .
 This package contains example data for artfastqgenerator.