Restricting search to CURRENT branch. (
wip/fastqc | | Quality control tool for high throughput sequence data |
wip/py-dnaio | | Read and write FASTQ and FASTA files |
wip/readseq | | Read and reformat biosequences, Java command-line version |
wip/pkg-dev | | Scripts to automate common tasks in pkgsrc development |
biology/biolibc | | Low-level high-performance bioinformatics library |
biology/plink | | Whole-genome association analysis toolset |
biology/gffread | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
biology/bedtools | | Swiss army knife for genome arithmetic |
biology/vcf-split | | Split a multi-sample VCF into single-sample VCFs |
archivers/libaec | | Adaptive entropy coding library |
biology/biolibc-tools | | High-performance bioinformatics tools based on biolibc |
wip/canu | | Single molecule sequence assembler for genomes large and small |
biology/fastp | | Ultra-fast all-in-one FASTQ preprocessor |
biology/canu | | Single molecule sequence assembler for genomes large and small |
security/munge | | Authentication service for creating and validating credentials |
biology/samtools | | Tools for manipulating sequence alignment maps |
biology/atac-seq | | Core tools needed for ATAC-Seq analysis |
www/webbrowser | | Proxy script for launching best available web browser |
devel/simde | | Header-only library for SIMD intrinsics |
wip/libgtextutils | | Gordon text utilities |
devel/libgtextutils | | Gordon text utilities |
math/basic-stats | | Command-line tool to perform basic statistics on tabular data |
biology/kallisto | | Quantify abundances of transcripts from RNA-Seq data |
biology/htslib | | C library for high-throughput sequencing data formats |
wip/vcf2hap | | Generate .hap file from VCF for haplohseq |
wip/plasm | | Portable Assembler |
wip/fasda | | Fast and simple differential analysis |
biology/generand | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/hisat2 | | Alignment program for mapping next-generation sequencing reads |
biology/fastx-toolkit | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
biology/cdhit | | Clustering and comparing protein or nucleotide sequences |
biology/vsearch | | Versatile open-source tool for metagenomics |
devel/libxtend | | Miscellaneous functions to extend libc |
wip/stacks | | Software pipeline for building loci from short-read sequences |
wip/brain-mesh-builder | | Surface mesh building based on 3-dimensional image stacks |
wip/py-macs2 | | Algorithm for identifying transcription factor binding sites |
wip/samtools | | Tools for manipulating sequence alignment maps |
wip/vcf-split | | Split a multi-sample VCF into single-sample VCFs |
wip/cut-and-run | | Split a text file into segments and process in parallel |
wip/ncbi-blast+ | | NCBI implementation of Basic Local Alignment Search Tool |
wip/py-dna-features-viewer | | Python library to visualize DNA features, e.g. GenBank or Gff files |
wip/py-bcbio-gff | | Read and write Generic Feature Format (GFF) with Biopython integration |
wip/auto-admin | | Portable tools for automating systems management |
wip/libpare | | Pointer Array Regular Expressions |
wip/fastq-trim | | Lightening fast sequence read trimmer |
wip/py-macs3 | | Peak caller aimed at transcription factor binding sites |
wip/microsynteny-tools | | Tools for exploring microsyntenic differences among species |
wip/fastp | | Ultra-fast all-in-one FASTQ preprocessor |
wip/atac-seq | | Core tools needed for ATAC-Seq analysis |
wip/hisat2 | | Alignment program for mapping next-generation sequencing reads |
wip/spcm | | Simple, portable cluster management |
wip/wip-tools | | Tools for developing wip packages |
wip/fbsd2pkg | | Convert a FreeBSD port framework to a pkgsrc package |
wip/py-pysam | | Python module for reading, manipulating and writing genomic data sets |
wip/bio-mocha | | Bcftools plugin for mosaic chromosomal alteration analysis |
wip/mst-bench | | Maximum sustainable throughput benchmark |
wip/vsearch | | Versatile open-source tool for metagenomics |
wip/lpjs | | Lightweight, Portable Job Scheduler |
wip/twintk | | Terminal Windows Toolkit |
wip/fastx-toolkit | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
wip/seqtk | | Tool for processing sequences in FASTA/FASTQ format |
wip/py-htseq | | Python library to facilitate programmatic analysis of sequence data |
wip/webbrowser | | Proxy script for launching best available web browser |
wip/rna-seq | | Core tools needed for RNA-Seq analysis |
wip/peak-classifier | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
wip/gffread | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
wip/basic-stats | | Command-line tool to perform basic statistics on tabular data |
wip/htslib | | C library for high-throughput sequencing data formats |
wip/auto-dev | | Tools for automating code development and documentation |
wip/libxtend | | Miscellaneous functions to extend libc |
wip/papp | | Assembly Preprocessor |
wip/bowtie2 | | Ultrafast, memory-efficient short read aligner |
wip/biolibc | | Low-level high-performance bioinformatics library |
wip/docviewer | | Generic command to automatically select a document viewer |
wip/biolibc-tools | | High-performance bioinformatics tools based on biolibc |
biology/fastqc | | Quality control tool for high throughput sequence data |
biology/fasda | | Fast and simple differential analysis |
biology/ad2vcf | | Add allelic depth info from a SAM stream to a VCF file |
biology/bwa | | Map low-divergent sequences against a large reference genome |
biology/igv | | Visualization tool for genomic datasets |
biology/py-macs2 | | Algorithm for identifying transcription factor binding sites |
biology/vcf2hap | | Generate .hap file from VCF for haplohseq |
biology/peak-classifier | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
wip/ape | | Another Programmers Editor |
biology/ncbi-blast+ | | NCBI implementation of Basic Local Alignment Search Tool |
biology/stacks | | Software pipeline for building loci from short-read sequences |
biology/plinkseq | | C/C++ library for working with human genetic variation data |
biology/bowtie2 | | Ultrafast, memory-efficient short read aligner |
biology/fastq-trim | | Lightening fast sequence read trimmer |
wip/kallisto | | Quantify abundances of transcripts from RNA-Seq data |
wip/bwa | | Map low-divergent sequences against a large reference genome |
biology/seqtk | | Tool for processing sequences in FASTA/FASTQ format |
sysutils/auto-admin | | Portable tools for automating systems management |
wip/npmount | | Command line tool for non-privileged [un]mount |
wip/qmediamanager | | GUI tool for managing removable media |
wip/desktop-installer | | Quickly configure a NetBSD desktop system |
sysutils/devpub-mount | | NetBSD devpubd-based automounter |
sysutils/desktop-installer | | Quickly configure a NetBSD desktop system |
wip/devpub-mount | | NetBSD devpubd-based automounter |
biology/chip-seq | | Core tools needed for ChIP-Seq analysis |
sysutils/npmount | | Command line tool for non-privileged [un]mount |
sysutils/qmediamanager | | GUI tool for managing removable media |
wip/py-multiqc | | Aggregate bioinformatics analysis reports across samples and tools |
wip/stringtie | | Transcript assembly and quantification for RNA-seq |
devel/py-rich-click | | Format click help output nicely with rich |
graphics/py-spectra | | Color scales and color conversion made easy for Python |
archivers/py-lzstring | | LZ-based in-memory string compression |
biology/py-multiqc | | Aggregate bioinformatics analysis reports across samples and tools |
devel/py-capturer | | Easily capture stdout/stderr of the current process and subprocesses |
devel/py-verboselogs | | Extend Python logging module to add the log levels |
devel/py-coloredlogs | | Colored terminal output for Pythons logging module |
math/py-colormath | | Module that spares the user from directly dealing with color math |
wip/rna-star | | Spliced Transcripts Alignment to a Reference |
biology/rna-star | | Spliced Transcripts Alignment to a Reference |
textproc/py-humanfriendly | | Human friendly output for text interfaces using Python |
biology/stringtie | | Transcript assembly and quantification for RNA-seq |
wip/sra-tools | | NCBIs toolkit for handling data in INSDC Sequence Read Archives |
biology/bcftools | | Tools for manipulating BCF and VCF variant call files |
biology/rna-seq | | Core tools needed for RNA-Seq analysis |
biology/sra-tools | | NCBIs toolkit for handling data in INSDC Sequence Read Archives |
sysutils/runas | | Wrapper around su for running a command as another user |
wip/gcta | | Genome-wide Complex Trait Analysis |
wip/bifrost | | Parallel construction, indexing and querying of de Bruijn graphs |
biology/py-bcbio-gff | | Read and write Generic Feature Format (GFF) with Biopython integration |
biology/microsynteny-tools | | Tools for exploring microsyntenic differences among species |
biology/py-dna-features-viewer | | Python library to visualize DNA features, e.g. GenBank or Gff files |
wip/py-cython-legacy | | C-Extensions for Python |
wip/py-pybigwig | | Python access to bigWig files using libBigWig |
wip/chip-seq | | Core tools needed for ChIP-Seq analysis |
math/armadillo | | C++ linear algebra library |
devel/py-cykhash | | Cython equivalent to khash-sets/maps |
biology/py-macs3 | | Peak caller aimed at transcription factor binding sites |
wip/biostar-tools | | Meta-package for Biostar Handbook tools |
wip/bedtools | | Swiss army knife for genome arithmetic |
wip/runas | | Wrapper around su for running a command as another user |
wip/munge | | Authentication service for creating and validating credentials |
wip/ad2vcf | | Add allelic depth info from a SAM stream to a VCF file |
biology/trimmomatic | | Flexible read trimming tool for Illumina NGS data |