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SDG Paper Datasets
This resource contains dataset used in the paper describing the SDG software framework: "A Sequence Distance Graph framework for genome assembly and analysis".... -
Mapping data: two point linkage estimates and standard errors.
Composite two point linkage estimates and standard errors for each linkage group in the Culex pipiens genetic map. -
Next-generation sequencing read statistics and sequencing coverage for the sa...
Next-generation sequencing read statistics and sequencing coverage for the sample datasets. -
r37980778c78--b339d08c132b9790545d072a0af001db
Prokaryote genomes containing at least 2 kbp of likely human originated (LHO) sequence. -
Non-mammal vertebrate genomes containing at least 2 kbp of likely human origi...
Non-mammal vertebrate genomes containing at least 2 kbp of likely human originated (LHO) sequence. -
Mammalian genomes containing at least 2 kbp of likely human originated (LHO) ...
Mammalian genomes containing at least 2 kbp of likely human originated (LHO) sequence. -
Non-vertebrate eukaryote genomes containing at least 2 kbp of likely human or...
Non-vertebrate eukaryote genomes containing at least 2 kbp of likely human originated (LHO) sequence. -
dedup_wf_001--98455ac5dfa7764a6c73f7b07bdb595e
CamDro2 genome gzipped (www.gzip.org/ ) FASTA file, chromosomes are identified by >1,>2,...,>36,>X (for chromosomes 1,2,...,36,X). There is no Y chromosome as the... -
r37980778c78--89287807c0558934d6d495a01f92839e
Contamination in genome assembly can lead to wrong or confusing results when using such genome as reference in sequence comparison. Although bacterial contamination is well... -
r37980778c78--94546267b40558d3bbb1db4e32329c1a
This is the version of riboSeed referenced in the bioRxiv manuscript and in journal submission. Future releases will be linked directly with Zenodo, but because this was set up... -
gapFinisher: A reliable gap filling pipeline for SSPACE-LongRead scaffolder o...
Unknown sequences, or gaps, are present in many published genomes across public databases. Gap filling is an important finishing step in de novo genome assembly, especially in...