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R-geepack-devel-1.2.1-2.lbn25.x86_64
Development files for R-geepack.
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R-geepack-devel-1.3.2-5.fc36.x86_64
Development files for R-geepack.
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BastionLinux 36
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R-GeneR-2.24.0-11.lbn19.x86_64
Package manipulating nucleotidic sequences (Embl, Fasta, GenBank).
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BastionLinux 19
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R-GenomeInfoDb-1.8.7-1.lbn19.noarch
The Seqnames package contains data and functions that define and allow
translation between different chromosome sequence naming conventions (e.g.,
"chr1" versus "1"), including a function that attempts to place sequence
names in their natural, rather than lexicographic, order.
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R-GenomeInfoDb-1.14.0-1.lbn25.noarch
The Seqnames package contains data and functions that define and allow
translation between different chromosome sequence naming conventions (e.g.,
"chr1" versus "1"), including a function that attempts to place sequence
names in their natural, rather than lexicographic, order.
Located in
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BastionLinux 25
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R-GenomeInfoDb-1.28.0-3.fc36.noarch
The Seqnames package contains data and functions that define and allow
translation between different chromosome sequence naming conventions (e.g.,
"chr1" versus "1"), including a function that attempts to place sequence
names in their natural, rather than lexicographic, order.
Located in
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BastionLinux 36
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R-GenomeInfoDbData-1.0.0-1.lbn25.noarch
Files for mapping between NCBI taxonomy ID and species. Used by functions
in the GenomeInfoDb package.
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BastionLinux 25
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R-GenomeInfoDbData-1.2.6-3.fc36.noarch
Files for mapping between NCBI taxonomy ID and species. Used by functions
in the GenomeInfoDb package.
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BastionLinux 36
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R-GenomicAlignments-1.28.0-3.fc36.x86_64
Provides efficient containers for storing and manipulating short genomic
alignments (typically obtained by aligning short reads to a reference genome).
This includes read counting, computing the coverage, junction detection, and
working with the nucleotide content of the alignments.
Located in
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BastionLinux 36
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R-GenomicAlignments-1.14.1-1.lbn25.x86_64
Provides efficient containers for storing and manipulating short genomic
alignments (typically obtained by aligning short reads to a reference genome).
This includes read counting, computing the coverage, junction detection, and
working with the nucleotide content of the alignments.
Located in
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BastionLinux 25
