sysutils/qmediamanager [CURRENT] | | GUI tool for managing removable media |
wip/py-multiqc [CURRENT] | | Aggregate bioinformatics analysis reports across samples and tools |
devel/py-verboselogs [CURRENT] | | Extend Python logging module to add the log levels |
biology/rna-star [CURRENT] | | Spliced Transcripts Alignment to a Reference |
graphics/py-spectra [CURRENT] | | Color scales and color conversion made easy for Python |
devel/py-coloredlogs [CURRENT] | | Colored terminal output for Pythons logging module |
wip/gcta [CURRENT] | | Genome-wide Complex Trait Analysis |
wip/fastaunique [CURRENT] | | Sort and uniq fasta files |
devel/py-rich-click [CURRENT] | | Format click help output nicely with rich |
biology/py-multiqc [CURRENT] | | Aggregate bioinformatics analysis reports across samples and tools |
math/py-colormath [CURRENT] | | Module that spares the user from directly dealing with color math |
devel/py-capturer [CURRENT] | | Easily capture stdout/stderr of the current process and subprocesses |
archivers/py-lzstring [CURRENT] | | LZ-based in-memory string compression |
textproc/py-humanfriendly [CURRENT] | | Human friendly output for text interfaces using Python |
biology/stringtie [CURRENT] | | Transcript assembly and quantification for RNA-seq |
wip/sra-tools [CURRENT] | | NCBIs toolkit for handling data in INSDC Sequence Read Archives |
biology/bcftools [CURRENT] | | Tools for manipulating BCF and VCF variant call files |
biology/sra-tools [CURRENT] | | NCBIs toolkit for handling data in INSDC Sequence Read Archives |
wip/gemma [CURRENT] | | Genome-wide Efficient Mixed Model Association |
biology/rna-seq [CURRENT] | | Core tools needed for RNA-Seq analysis |
sysutils/runas [CURRENT] | | Wrapper around su for running a command as another user |
devel/simde [CURRENT] | | Header-only library for SIMD intrinsics |
wip/structure [CURRENT] | | Multi-locus genotype data to investigate population structure |
www/webbrowser [CURRENT] | | Proxy script for launching best available web browser |
biology/atac-seq [CURRENT] | | Core tools needed for ATAC-Seq analysis |
security/munge [CURRENT] | | Authentication service for creating and validating credentials |
biology/samtools [CURRENT] | | Tools for manipulating sequence alignment maps |
wip/samtools [CURRENT] | | Tools for manipulating sequence alignment maps |
wip/fastqc [CURRENT] | | Quality control tool for high throughput sequence data |
wip/vcf-split [CURRENT] | | Split a multi-sample VCF into single-sample VCFs |
wip/muscle [CURRENT] | | MUltiple Sequence Comparison by Log-Expectation |
biology/ncbi-blast+ [CURRENT] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/bowtie2 [CURRENT] | | Ultrafast, memory-efficient short read aligner |
wip/kallisto [CURRENT] | | Quantify abundances of transcripts from RNA-Seq data |
wip/bwa [CURRENT] | | Map low-divergent sequences against a large reference genome |
wip/bifrost [CURRENT] | | Parallel construction, indexing and querying of de Bruijn graphs |
biology/mca-calling [CURRENT] | | Core tools for Mosaic Chromosomal Alteration event calling |
biology/bio-mocha [CURRENT] | | Bcftools plugin for mosaic chromosomal alteration analysis |
biology/bcf-score [CURRENT] | | Bcftools plugin for mosaic chromosomal alteration analysis |
wip/trimadap [CURRENT] | | Trim adapter sequences from Illumina data using heuristic rules |
wip/fastool [CURRENT] | | Simple and quick FastQ and FastA tool for file reading and conversion |
wip/detab [CURRENT] | | Replace tabs with spaces in a text file |
wip/pear [CURRENT] | | Memory-efficient and highly accurate pair-end read merger |
biology/trimmomatic [CURRENT] | | Flexible read trimming tool for Illumina NGS data |
wip/biostar-tools [CURRENT] | | Meta-package for Biostar Handbook tools |
biology/seqtk [CURRENT] | | Tool for processing sequences in FASTA/FASTQ format |
devel/py-cykhash [CURRENT] | | Cython equivalent to khash-sets/maps |
biology/py-macs3 [CURRENT] | | Peak caller aimed at transcription factor binding sites |
math/armadillo [CURRENT] | | C++ linear algebra library |
wip/chip-seq [CURRENT] | | Core tools needed for ChIP-Seq analysis |
wip/bedtools [CURRENT] | | Swiss army knife for genome arithmetic |
sysutils/auto-admin [CURRENT] | | Portable tools for automating systems management |
wip/npmount [CURRENT] | | Command line tool for non-privileged [un]mount |
wip/py-cython-legacy [CURRENT] | | C-Extensions for Python |
wip/py-orca [CURRENT] | | Python library for task orchestration |
wip/preseq [CURRENT] | | Predict yield of distinct reads from a genomic library |
wip/qmediamanager [CURRENT] | | GUI tool for managing removable media |
biology/py-bcbio-gff [CURRENT] | | Read and write Generic Feature Format (GFF) with Biopython integration |
devel/py-orca [CURRENT] | | Python library for task orchestration |
sysutils/desktop-installer [CURRENT] | | Quickly configure a NetBSD desktop system |
biology/chip-seq [CURRENT] | | Core tools needed for ChIP-Seq analysis |
biology/microsynteny-tools [CURRENT] | | Tools for exploring microsyntenic differences among species |
sysutils/npmount [CURRENT] | | Command line tool for non-privileged [un]mount |
wip/desktop-installer [CURRENT] | | Quickly configure a NetBSD desktop system |
wip/devpub-mount [CURRENT] | | NetBSD devpubd-based automounter |
sysutils/devpub-mount [CURRENT] | | NetBSD devpubd-based automounter |
biology/py-dna-features-viewer [CURRENT] | | Python library to visualize DNA features, e.g. GenBank or Gff files |
wip/stringtie [CURRENT] | | Transcript assembly and quantification for RNA-seq |
wip/cut-and-run [CURRENT] | | Split a text file into segments and process in parallel |
wip/ncbi-blast+ [CURRENT] | | NCBI implementation of Basic Local Alignment Search Tool |
wip/ti99sim [CURRENT] | | SDL-based TI-99/4a simulator |
wip/py-macs2 [CURRENT] | | Algorithm for identifying transcription factor binding sites |
wip/py-eggnog-mapper [CURRENT] | | Fast functional annotation of novel DNA or protein sequences |
wip/py-htseq [CURRENT] | | Python library to facilitate programmatic analysis of sequence data |
wip/famsa [CURRENT] | | Algorithm for large-scale multiple sequence alignments |
wip/rsem [CURRENT] | | RNA-Seq by Expectation-Maximization |
wip/stacks [CURRENT] | | Software pipeline for building loci from short-read sequences |
devel/libxtend [CURRENT] | | Miscellaneous functions to extend libc |
biology/fastx-toolkit [CURRENT] | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
biology/cdhit [CURRENT] | | Clustering and comparing protein or nucleotide sequences |
biology/hisat2 [CURRENT] | | Alignment program for mapping next-generation sequencing reads |
biology/vsearch [CURRENT] | | Versatile open-source tool for metagenomics |
biology/generand [CURRENT] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
wip/fasda [CURRENT] | | Fast and simple differential analysis |
wip/plasm [CURRENT] | | Portable Assembler |
biology/htslib [CURRENT] | | C library for high-throughput sequencing data formats |
biology/kallisto [CURRENT] | | Quantify abundances of transcripts from RNA-Seq data |
wip/canu [CURRENT] | | Single molecule sequence assembler for genomes large and small |
wip/munge [CURRENT] | | Authentication service for creating and validating credentials |
wip/metal [CURRENT] | | Meta-analysis of genomewide association scans |
wip/auto-admin [CURRENT] | | Portable tools for automating systems management |
wip/centrifuge [CURRENT] | | Novel microbial classification engine |
math/basic-stats [CURRENT] | | Command-line tool to perform basic statistics on tabular data |
wip/py-dna-features-viewer [CURRENT] | | Python library to visualize DNA features, e.g. GenBank or Gff files |
wip/py-bcbio-gff [CURRENT] | | Read and write Generic Feature Format (GFF) with Biopython integration |
biology/fastp [CURRENT] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/canu [CURRENT] | | Single molecule sequence assembler for genomes large and small |
wip/webbrowser [CURRENT] | | Proxy script for launching best available web browser |
devel/libgtextutils [CURRENT] | | Gordon text utilities |
wip/libgtextutils [CURRENT] | | Gordon text utilities |
wip/brain-mesh-builder [CURRENT] | | Surface mesh building based on 3-dimensional image stacks |
wip/libpare [CURRENT] | | Pointer Array Regular Expressions |
wip/fastq-trim [CURRENT] | | Lightening fast sequence read trimmer |
wip/fastp [CURRENT] | | Ultra-fast all-in-one FASTQ preprocessor |
wip/runas [CURRENT] | | Wrapper around su for running a command as another user |
wip/microsynteny-tools [CURRENT] | | Tools for exploring microsyntenic differences among species |
wip/slclust [CURRENT] | | Single-linkage clustering with Jaccard similarity |
wip/tabixpp [CURRENT] | | C++ wrapper to tabix indexer |
biology/biolibc-tools [CURRENT] | | High-performance bioinformatics tools based on biolibc |
wip/atac-seq [CURRENT] | | Core tools needed for ATAC-Seq analysis |
archivers/libaec [CURRENT] | | Adaptive entropy coding library |
wip/hisat2 [CURRENT] | | Alignment program for mapping next-generation sequencing reads |
wip/spcm [CURRENT] | | Simple, portable cluster management |
wip/wip-tools [CURRENT] | | Tools for developing wip packages |
biology/vcf-split [CURRENT] | | Split a multi-sample VCF into single-sample VCFs |
wip/p5-transdecoder [CURRENT] | | Identify candidate coding regions within transcript sequences |
wip/filevercmp [CURRENT] | | Filevercmp function as in sort --version-sort |
biology/bedtools [CURRENT] | | Swiss army knife for genome arithmetic |
wip/fbsd2pkg [CURRENT] | | Convert a FreeBSD port framework to a pkgsrc package |
wip/epacts [CURRENT] | | Efficient and Parallelizable Association Container Toolbox |
wip/py-pysam [CURRENT] | | Python module for reading, manipulating and writing genomic data sets |
wip/mst-bench [CURRENT] | | Maximum sustainable throughput benchmark |
wip/bio-mocha [CURRENT] | | Bcftools plugin for mosaic chromosomal alteration analysis |
wip/vsearch [CURRENT] | | Versatile open-source tool for metagenomics |
wip/lpjs [CURRENT] | | Lightweight, Portable Job Scheduler |
biology/gffread [CURRENT] | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
biology/plink [CURRENT] | | Whole-genome association analysis toolset |
biology/biolibc [CURRENT] | | Low-level high-performance bioinformatics library |
wip/bpcscripts [CURRENT] | | Gast Illumina processing |
wip/pkg-dev [CURRENT] | | Scripts to automate common tasks in pkgsrc development |
wip/twintk [CURRENT] | | Terminal Windows Toolkit |
wip/bcftools [CURRENT] | | Tools for manipulating BCF and VCF variant call files |
wip/vcf2hap [CURRENT] | | Generate .hap file from VCF for haplohseq |
wip/fastx-toolkit [CURRENT] | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
wip/rna-seq [CURRENT] | | Core tools needed for RNA-Seq analysis |
wip/seqtk [CURRENT] | | Tool for processing sequences in FASTA/FASTQ format |
wip/ad2vcf [CURRENT] | | Add allelic depth info from a SAM stream to a VCF file |
wip/peak-classifier [CURRENT] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
wip/readseq [CURRENT] | | Read and reformat biosequences, Java command-line version |
wip/basic-stats [CURRENT] | | Command-line tool to perform basic statistics on tabular data |
wip/htslib [CURRENT] | | C library for high-throughput sequencing data formats |
wip/auto-dev [CURRENT] | | Tools for automating code development and documentation |
wip/gffread [CURRENT] | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
wip/papp [CURRENT] | | Assembly Preprocessor |
wip/libxtend [CURRENT] | | Miscellaneous functions to extend libc |
wip/biolibc [CURRENT] | | Low-level high-performance bioinformatics library |
wip/bowtie2 [CURRENT] | | Ultrafast, memory-efficient short read aligner |
wip/docviewer [CURRENT] | | Generic command to automatically select a document viewer |
wip/biolibc-tools [CURRENT] | | High-performance bioinformatics tools based on biolibc |
wip/generand [CURRENT] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/ad2vcf [CURRENT] | | Add allelic depth info from a SAM stream to a VCF file |
wip/fastahack [CURRENT] | | Utilities for indexing and sequence extraction from FASTA files |
biology/vcf2hap [CURRENT] | | Generate .hap file from VCF for haplohseq |
biology/fasda [CURRENT] | | Fast and simple differential analysis |
wip/py-macs3 [CURRENT] | | Peak caller aimed at transcription factor binding sites |
wip/bolt-lmm [CURRENT] | | Statistics for testing association between phenotype and genotypes |
wip/rna-star [CURRENT] | | Spliced Transcripts Alignment to a Reference |
wip/fasttree [CURRENT] | | Approximately-maximum-likelihood phylogenetic trees from alignments |
wip/subread [CURRENT] | | High-performance read alignment, quantification and mutation discovery |
wip/py-pybigwig [CURRENT] | | Python access to bigWig files using libBigWig |
wip/igv [CURRENT] | | Visualization tool for genomic datasets |
wip/gmap [CURRENT] | | Genomic Mapping and Alignment Program for mRNA and EST Sequences |
biology/fastqc [CURRENT] | | Quality control tool for high throughput sequence data |
biology/peak-classifier [CURRENT] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/igv [CURRENT] | | Visualization tool for genomic datasets |
biology/bwa [CURRENT] | | Map low-divergent sequences against a large reference genome |
biology/py-macs2 [CURRENT] | | Algorithm for identifying transcription factor binding sites |
wip/rainbow [CURRENT] | | Short reads clustering and local assembly |
wip/bcf-score [CURRENT] | | Bcftools plugin for mosaic chromosomal alteration analysis |
wip/ape [CURRENT] | | Another Programmers Editor |
biology/fastq-trim [CURRENT] | | Lightening fast sequence read trimmer |
biology/haplohseq [CURRENT] | | Identify regions of allelic imbalance |
wip/py-dnaio [CURRENT] | | Read and write FASTQ and FASTA files |
biology/plinkseq [CURRENT] | | C/C++ library for working with human genetic variation data |
biology/stacks [CURRENT] | | Software pipeline for building loci from short-read sequences |
biology/bwa [pkgsrc-2017Q4] | | Map low-divergent sequences against a large reference genome |
devel/py-xopen [pkgsrc-2017Q4] | | Open compressed files transparently |
security/munge [pkgsrc-2018Q1] | | Authentication service for creating and validating credentials |
parallel/slurm [pkgsrc-2018Q1] | | Simple Linux Utility for Resource Management |
textproc/man2html [pkgsrc-2018Q1] | | Convert nroff(1) man pages to HTML |
biology/bwa [pkgsrc-2018Q1] | | Map low-divergent sequences against a large reference genome |
devel/py-xopen [pkgsrc-2018Q1] | | Open compressed files transparently |
biology/htslib [pkgsrc-2018Q2] | | C library for high-throughput sequencing data formats |
biology/samtools [pkgsrc-2018Q2] | | Tools for manipulating next-generation sequencing data |
biology/bwa [pkgsrc-2018Q2] | | Map low-divergent sequences against a large reference genome |
security/munge [pkgsrc-2018Q2] | | Authentication service for creating and validating credentials |
biology/ncbi-blast+ [pkgsrc-2018Q2] | | NCBI implementation of Basic Local Alignment Search Tool |
parallel/slurm-wlm [pkgsrc-2018Q2] | | Simple Linux Utility for Resource Management |
parallel/ganglia-monitor-core [pkgsrc-2018Q2] | | Ganglia cluster monitor, monitoring daemon |
textproc/man2html [pkgsrc-2018Q2] | | Convert nroff(1) man pages to HTML |
devel/py-xopen [pkgsrc-2018Q2] | | Open compressed files transparently |
security/munge [pkgsrc-2018Q3] | | Authentication service for creating and validating credentials |
textproc/man2html [pkgsrc-2018Q3] | | Convert nroff(1) man pages to HTML |
parallel/ganglia-monitor-core [pkgsrc-2018Q3] | | Ganglia cluster monitor, monitoring daemon |
biology/ncbi-blast+ [pkgsrc-2018Q3] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/samtools [pkgsrc-2018Q3] | | Tools for manipulating next-generation sequencing data |
biology/htslib [pkgsrc-2018Q3] | | C library for high-throughput sequencing data formats |
devel/py-xopen [pkgsrc-2018Q3] | | Open compressed files transparently |
biology/bwa [pkgsrc-2018Q3] | | Map low-divergent sequences against a large reference genome |
biology/trimmomatic [pkgsrc-2018Q3] | | Flexible read trimming tool for Illumina NGS data |
parallel/slurm-wlm [pkgsrc-2018Q3] | | Simple Linux Utility for Resource Management |
security/munge [pkgsrc-2018Q4] | | Authentication service for creating and validating credentials |
textproc/man2html [pkgsrc-2018Q4] | | Convert nroff(1) man pages to HTML |
biology/kallisto [pkgsrc-2018Q4] | | Quantify abundances of transcripts from RNA-Seq data |
biology/ncbi-blast+ [pkgsrc-2018Q4] | | NCBI implementation of Basic Local Alignment Search Tool |
parallel/ganglia-monitor-core [pkgsrc-2018Q4] | | Ganglia cluster monitor, monitoring daemon |
biology/htslib [pkgsrc-2018Q4] | | C library for high-throughput sequencing data formats |
parallel/slurm-wlm [pkgsrc-2018Q4] | | Simple Linux Utility for Resource Management |
biology/samtools [pkgsrc-2018Q4] | | Tools for manipulating next-generation sequencing data |
biology/trimmomatic [pkgsrc-2018Q4] | | Flexible read trimming tool for Illumina NGS data |
devel/py-xopen [pkgsrc-2018Q4] | | Open compressed files transparently |
biology/stacks [pkgsrc-2018Q4] | | Software pipeline for building loci from short-read sequences |
biology/bwa [pkgsrc-2018Q4] | | Map low-divergent sequences against a large reference genome |
devel/libctl [pkgsrc-2019Q1] | | Guile-based flexible control file library for scientific simulations |
textproc/man2html [pkgsrc-2019Q1] | | Convert nroff(1) man pages to HTML |
biology/cdhit [pkgsrc-2019Q1] | | Clustering and comparing protein or nucleotide sequences |
biology/hisat2 [pkgsrc-2019Q1] | | Alignment program for mapping next-generation sequencing reads |
biology/kallisto [pkgsrc-2019Q1] | | Quantify abundances of transcripts from RNA-Seq data |
biology/trimmomatic [pkgsrc-2019Q1] | | Flexible read trimming tool for Illumina NGS data |
biology/stacks [pkgsrc-2019Q1] | | Software pipeline for building loci from short-read sequences |
biology/bwa [pkgsrc-2019Q1] | | Map low-divergent sequences against a large reference genome |
biology/canu [pkgsrc-2019Q1] | | Single molecule sequence assembler for genomes large and small |
biology/plink [pkgsrc-2019Q1] | | Whole-genome association analysis toolset |
biology/plinkseq [pkgsrc-2019Q1] | | C/C++ library for working with human genetic variation data |
biology/samtools [pkgsrc-2019Q1] | | Tools for manipulating next-generation sequencing data |
biology/htslib [pkgsrc-2019Q1] | | C library for high-throughput sequencing data formats |
biology/ncbi-blast+ [pkgsrc-2019Q1] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/bcftools [pkgsrc-2019Q1] | | Calling and manipulating files VCF and BCF formats |
devel/swig2 [pkgsrc-2019Q1] | | Simplified Wrapper and Interface Generator (version 2) |
security/munge [pkgsrc-2019Q1] | | Authentication service for creating and validating credentials |
parallel/ganglia-monitor-core [pkgsrc-2019Q1] | | Ganglia cluster monitor, monitoring daemon |
parallel/slurm-wlm [pkgsrc-2019Q1] | | Simple Linux Utility for Resource Management |
math/arpack [pkgsrc-2019Q1] | | Library of subroutines to solve eigenvalue problems |
devel/py-xopen [pkgsrc-2019Q1] | | Open compressed files transparently |
biology/samtools [pkgsrc-2019Q2] | | Tools for manipulating next-generation sequencing data |
biology/plinkseq [pkgsrc-2019Q2] | | C/C++ library for working with human genetic variation data |
biology/trimmomatic [pkgsrc-2019Q2] | | Flexible read trimming tool for Illumina NGS data |
biology/fastp [pkgsrc-2019Q2] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/hisat2 [pkgsrc-2019Q2] | | Alignment program for mapping next-generation sequencing reads |
biology/plink [pkgsrc-2019Q2] | | Whole-genome association analysis toolset |
biology/cdhit [pkgsrc-2019Q2] | | Clustering and comparing protein or nucleotide sequences |
devel/libctl [pkgsrc-2019Q2] | | Guile-based flexible control file library for scientific simulations |
biology/ncbi-blast+ [pkgsrc-2019Q2] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/bcftools [pkgsrc-2019Q2] | | Calling and manipulating files VCF and BCF formats |
biology/canu [pkgsrc-2019Q2] | | Single molecule sequence assembler for genomes large and small |
parallel/slurm-wlm [pkgsrc-2019Q2] | | Simple Linux Utility for Resource Management |
biology/stacks [pkgsrc-2019Q2] | | Software pipeline for building loci from short-read sequences |
parallel/ganglia-monitor-core [pkgsrc-2019Q2] | | Ganglia cluster monitor, monitoring daemon |
archivers/libaec [pkgsrc-2019Q2] | | Adaptive entropy coding library |
devel/swig2 [pkgsrc-2019Q2] | | Simplified Wrapper and Interface Generator (version 2) |
biology/bwa [pkgsrc-2019Q2] | | Map low-divergent sequences against a large reference genome |
biology/htslib [pkgsrc-2019Q2] | | C library for high-throughput sequencing data formats |
textproc/man2html [pkgsrc-2019Q2] | | Convert nroff(1) man pages to HTML |
devel/py-xopen [pkgsrc-2019Q2] | | Open compressed files transparently |
biology/vsearch [pkgsrc-2019Q2] | | Versatile open-source tool for metagenomics |
biology/kallisto [pkgsrc-2019Q2] | | Quantify abundances of transcripts from RNA-Seq data |
math/arpack [pkgsrc-2019Q2] | | Library of subroutines to solve eigenvalue problems |
security/munge [pkgsrc-2019Q2] | | Authentication service for creating and validating credentials |
devel/R-rematch [pkgsrc-2019Q3] | | Match regular expressions with a nicer API |
parallel/ganglia-monitor-core [pkgsrc-2019Q3] | | Ganglia cluster monitor, monitoring daemon |
math/arpack [pkgsrc-2019Q3] | | Library of subroutines to solve eigenvalue problems |
devel/swig2 [pkgsrc-2019Q3] | | Simplified Wrapper and Interface Generator (version 2) |
devel/libctl [pkgsrc-2019Q3] | | Guile-based flexible control file library for scientific simulations |
biology/kallisto [pkgsrc-2019Q3] | | Quantify abundances of transcripts from RNA-Seq data |
biology/cdhit [pkgsrc-2019Q3] | | Clustering and comparing protein or nucleotide sequences |
biology/stacks [pkgsrc-2019Q3] | | Software pipeline for building loci from short-read sequences |
biology/plink [pkgsrc-2019Q3] | | Whole-genome association analysis toolset |
biology/bcftools [pkgsrc-2019Q3] | | Calling and manipulating files VCF and BCF formats |
textproc/R-cellranger [pkgsrc-2019Q3] | | Translate spreadsheet cell ranges to rows and columns |
biology/htslib [pkgsrc-2019Q3] | | C library for high-throughput sequencing data formats |
biology/fastp [pkgsrc-2019Q3] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/canu [pkgsrc-2019Q3] | | Single molecule sequence assembler for genomes large and small |
biology/ncbi-blast+ [pkgsrc-2019Q3] | | NCBI implementation of Basic Local Alignment Search Tool |
parallel/slurm-wlm [pkgsrc-2019Q3] | | Simple Linux Utility for Resource Management |
textproc/man2html [pkgsrc-2019Q3] | | Convert nroff(1) man pages to HTML |
textproc/R-data.table [pkgsrc-2019Q3] | | Extension of data.frame |
security/munge [pkgsrc-2019Q3] | | Authentication service for creating and validating credentials |
archivers/libaec [pkgsrc-2019Q3] | | Adaptive entropy coding library |
biology/trimmomatic [pkgsrc-2019Q3] | | Flexible read trimming tool for Illumina NGS data |
biology/samtools [pkgsrc-2019Q3] | | Tools for manipulating next-generation sequencing data |
biology/bwa [pkgsrc-2019Q3] | | Map low-divergent sequences against a large reference genome |
biology/plinkseq [pkgsrc-2019Q3] | | C/C++ library for working with human genetic variation data |
biology/vsearch [pkgsrc-2019Q3] | | Versatile open-source tool for metagenomics |
biology/hisat2 [pkgsrc-2019Q3] | | Alignment program for mapping next-generation sequencing reads |
devel/py-xopen [pkgsrc-2019Q3] | | Open compressed files transparently |
biology/htslib [pkgsrc-2019Q4] | | C library for high-throughput sequencing data formats |
biology/kallisto [pkgsrc-2019Q4] | | Quantify abundances of transcripts from RNA-Seq data |
math/arpack [pkgsrc-2019Q4] | | Library of subroutines to solve eigenvalue problems |
textproc/man2html [pkgsrc-2019Q4] | | Convert nroff(1) man pages to HTML |
biology/stacks [pkgsrc-2019Q4] | | Software pipeline for building loci from short-read sequences |
textproc/R-data.table [pkgsrc-2019Q4] | | Extension of data.frame |
devel/swig2 [pkgsrc-2019Q4] | | Simplified Wrapper and Interface Generator (version 2) |
archivers/libaec [pkgsrc-2019Q4] | | Adaptive entropy coding library |
biology/cdhit [pkgsrc-2019Q4] | | Clustering and comparing protein or nucleotide sequences |
biology/fastp [pkgsrc-2019Q4] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/trimmomatic [pkgsrc-2019Q4] | | Flexible read trimming tool for Illumina NGS data |
devel/libctl [pkgsrc-2019Q4] | | Guile-based flexible control file library for scientific simulations |
devel/py-xopen [pkgsrc-2019Q4] | | Open compressed files transparently |
biology/bcftools [pkgsrc-2019Q4] | | Calling and manipulating files VCF and BCF formats |
biology/canu [pkgsrc-2019Q4] | | Single molecule sequence assembler for genomes large and small |
biology/bwa [pkgsrc-2019Q4] | | Map low-divergent sequences against a large reference genome |
biology/plinkseq [pkgsrc-2019Q4] | | C/C++ library for working with human genetic variation data |
biology/samtools [pkgsrc-2019Q4] | | Tools for manipulating next-generation sequencing data |
devel/R-rematch [pkgsrc-2019Q4] | | Match regular expressions with a nicer API |
security/munge [pkgsrc-2019Q4] | | Authentication service for creating and validating credentials |
biology/ncbi-blast+ [pkgsrc-2019Q4] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/vsearch [pkgsrc-2019Q4] | | Versatile open-source tool for metagenomics |
parallel/slurm-wlm [pkgsrc-2019Q4] | | Simple Linux Utility for Resource Management |
parallel/ganglia-monitor-core [pkgsrc-2019Q4] | | Ganglia cluster monitor, monitoring daemon |
textproc/R-cellranger [pkgsrc-2019Q4] | | Translate spreadsheet cell ranges to rows and columns |
biology/plink [pkgsrc-2019Q4] | | Whole-genome association analysis toolset |
biology/hisat2 [pkgsrc-2019Q4] | | Alignment program for mapping next-generation sequencing reads |
biology/bcftools [pkgsrc-2020Q1] | | Calling and manipulating files VCF and BCF formats |
devel/libctl [pkgsrc-2020Q1] | | Guile-based flexible control file library for scientific simulations |
textproc/R-cellranger [pkgsrc-2020Q1] | | Translate spreadsheet cell ranges to rows and columns |
devel/py-xopen [pkgsrc-2020Q1] | | Open compressed files transparently |
biology/samtools [pkgsrc-2020Q1] | | Tools for manipulating next-generation sequencing data |
biology/hisat2 [pkgsrc-2020Q1] | | Alignment program for mapping next-generation sequencing reads |
biology/cdhit [pkgsrc-2020Q1] | | Clustering and comparing protein or nucleotide sequences |
biology/trimmomatic [pkgsrc-2020Q1] | | Flexible read trimming tool for Illumina NGS data |
biology/stacks [pkgsrc-2020Q1] | | Software pipeline for building loci from short-read sequences |
biology/canu [pkgsrc-2020Q1] | | Single molecule sequence assembler for genomes large and small |
devel/swig2 [pkgsrc-2020Q1] | | Simplified Wrapper and Interface Generator (version 2) |
archivers/libaec [pkgsrc-2020Q1] | | Adaptive entropy coding library |
biology/fastp [pkgsrc-2020Q1] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/plinkseq [pkgsrc-2020Q1] | | C/C++ library for working with human genetic variation data |
security/munge [pkgsrc-2020Q1] | | Authentication service for creating and validating credentials |
biology/kallisto [pkgsrc-2020Q1] | | Quantify abundances of transcripts from RNA-Seq data |
biology/htslib [pkgsrc-2020Q1] | | C library for high-throughput sequencing data formats |
biology/vsearch [pkgsrc-2020Q1] | | Versatile open-source tool for metagenomics |
biology/ncbi-blast+ [pkgsrc-2020Q1] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/plink [pkgsrc-2020Q1] | | Whole-genome association analysis toolset |
biology/bwa [pkgsrc-2020Q1] | | Map low-divergent sequences against a large reference genome |
textproc/R-data.table [pkgsrc-2020Q1] | | Extension of data.frame |
parallel/ganglia-monitor-core [pkgsrc-2020Q1] | | Ganglia cluster monitor, monitoring daemon |
parallel/slurm-wlm [pkgsrc-2020Q1] | | Simple Linux Utility for Resource Management |
devel/R-rematch [pkgsrc-2020Q1] | | Match regular expressions with a nicer API |
textproc/man2html [pkgsrc-2020Q1] | | Convert nroff(1) man pages to HTML |
textproc/man2html [pkgsrc-2020Q2] | | Convert nroff(1) man pages to HTML |
textproc/R-cellranger [pkgsrc-2020Q2] | | Translate spreadsheet cell ranges to rows and columns |
biology/ncbi-blast+ [pkgsrc-2020Q2] | | NCBI implementation of Basic Local Alignment Search Tool |
devel/libctl [pkgsrc-2020Q2] | | Guile-based flexible control file library for scientific simulations |
devel/py-xopen [pkgsrc-2020Q2] | | Open compressed files transparently |
biology/samtools [pkgsrc-2020Q2] | | Tools for manipulating next-generation sequencing data |
biology/plinkseq [pkgsrc-2020Q2] | | C/C++ library for working with human genetic variation data |
biology/fastp [pkgsrc-2020Q2] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/stacks [pkgsrc-2020Q2] | | Software pipeline for building loci from short-read sequences |
biology/cdhit [pkgsrc-2020Q2] | | Clustering and comparing protein or nucleotide sequences |
biology/vsearch [pkgsrc-2020Q2] | | Versatile open-source tool for metagenomics |
biology/plink [pkgsrc-2020Q2] | | Whole-genome association analysis toolset |
biology/bcftools [pkgsrc-2020Q2] | | Calling and manipulating files VCF and BCF formats |
biology/canu [pkgsrc-2020Q2] | | Single molecule sequence assembler for genomes large and small |
archivers/libaec [pkgsrc-2020Q2] | | Adaptive entropy coding library |
parallel/ganglia-monitor-core [pkgsrc-2020Q2] | | Ganglia cluster monitor, monitoring daemon |
parallel/slurm-wlm [pkgsrc-2020Q2] | | Simple Linux Utility for Resource Management |
biology/htslib [pkgsrc-2020Q2] | | C library for high-throughput sequencing data formats |
biology/hisat2 [pkgsrc-2020Q2] | | Alignment program for mapping next-generation sequencing reads |
biology/trimmomatic [pkgsrc-2020Q2] | | Flexible read trimming tool for Illumina NGS data |
biology/kallisto [pkgsrc-2020Q2] | | Quantify abundances of transcripts from RNA-Seq data |
devel/swig2 [pkgsrc-2020Q2] | | Simplified Wrapper and Interface Generator (version 2) |
textproc/R-data.table [pkgsrc-2020Q2] | | Extension of data.frame |
security/munge [pkgsrc-2020Q2] | | Authentication service for creating and validating credentials |
biology/bwa [pkgsrc-2020Q2] | | Map low-divergent sequences against a large reference genome |
devel/R-rematch [pkgsrc-2020Q2] | | Match regular expressions with a nicer API |
devel/R-rematch [pkgsrc-2020Q3] | | Match regular expressions with a nicer API |
math/udunits [pkgsrc-2020Q3] | | Library and program for manipulating units of physical quantities |
parallel/ganglia-monitor-core [pkgsrc-2020Q3] | | Ganglia cluster monitor, monitoring daemon |
biology/plinkseq [pkgsrc-2020Q3] | | C/C++ library for working with human genetic variation data |
archivers/libaec [pkgsrc-2020Q3] | | Adaptive entropy coding library |
parallel/slurm-wlm [pkgsrc-2020Q3] | | Simple Linux Utility for Resource Management |
devel/swig2 [pkgsrc-2020Q3] | | Simplified Wrapper and Interface Generator (version 2) |
textproc/R-data.table [pkgsrc-2020Q3] | | Extension of data.frame |
biology/bcftools [pkgsrc-2020Q3] | | Tools for manipulating BCF and VCF variant call files |
biology/plink [pkgsrc-2020Q3] | | Whole-genome association analysis toolset |
biology/cdhit [pkgsrc-2020Q3] | | Clustering and comparing protein or nucleotide sequences |
biology/bwa [pkgsrc-2020Q3] | | Map low-divergent sequences against a large reference genome |
devel/libctl [pkgsrc-2020Q3] | | Guile-based flexible control file library for scientific simulations |
biology/stacks [pkgsrc-2020Q3] | | Software pipeline for building loci from short-read sequences |
biology/htslib [pkgsrc-2020Q3] | | C library for high-throughput sequencing data formats |
biology/fastp [pkgsrc-2020Q3] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/samtools [pkgsrc-2020Q3] | | Tools for manipulating sequence alignment maps |
biology/kallisto [pkgsrc-2020Q3] | | Quantify abundances of transcripts from RNA-Seq data |
biology/hisat2 [pkgsrc-2020Q3] | | Alignment program for mapping next-generation sequencing reads |
biology/ncbi-blast+ [pkgsrc-2020Q3] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/vsearch [pkgsrc-2020Q3] | | Versatile open-source tool for metagenomics |
textproc/man2html [pkgsrc-2020Q3] | | Convert nroff(1) man pages to HTML |
textproc/R-cellranger [pkgsrc-2020Q3] | | Translate spreadsheet cell ranges to rows and columns |
devel/py-xopen [pkgsrc-2020Q3] | | Open compressed files transparently |
biology/trimmomatic [pkgsrc-2020Q3] | | Flexible read trimming tool for Illumina NGS data |
biology/canu [pkgsrc-2020Q3] | | Single molecule sequence assembler for genomes large and small |
security/munge [pkgsrc-2020Q3] | | Authentication service for creating and validating credentials |
biology/cdhit [pkgsrc-2020Q4] | | Clustering and comparing protein or nucleotide sequences |
biology/samtools [pkgsrc-2020Q4] | | Tools for manipulating sequence alignment maps |
biology/kallisto [pkgsrc-2020Q4] | | Quantify abundances of transcripts from RNA-Seq data |
security/munge [pkgsrc-2020Q4] | | Authentication service for creating and validating credentials |
devel/swig2 [pkgsrc-2020Q4] | | Simplified Wrapper and Interface Generator (version 2) |
biology/stacks [pkgsrc-2020Q4] | | Software pipeline for building loci from short-read sequences |
devel/libctl [pkgsrc-2020Q4] | | Guile-based flexible control file library for scientific simulations |
biology/hisat2 [pkgsrc-2020Q4] | | Alignment program for mapping next-generation sequencing reads |
textproc/R-cellranger [pkgsrc-2020Q4] | | Translate spreadsheet cell ranges to rows and columns |
parallel/slurm-wlm [pkgsrc-2020Q4] | | Simple Linux Utility for Resource Management |
math/udunits [pkgsrc-2020Q4] | | Library and program for manipulating units of physical quantities |
biology/plinkseq [pkgsrc-2020Q4] | | C/C++ library for working with human genetic variation data |
biology/plink [pkgsrc-2020Q4] | | Whole-genome association analysis toolset |
biology/canu [pkgsrc-2020Q4] | | Single molecule sequence assembler for genomes large and small |
biology/bcftools [pkgsrc-2020Q4] | | Tools for manipulating BCF and VCF variant call files |
biology/fastp [pkgsrc-2020Q4] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/ncbi-blast+ [pkgsrc-2020Q4] | | NCBI implementation of Basic Local Alignment Search Tool |
archivers/libaec [pkgsrc-2020Q4] | | Adaptive entropy coding library |
sysutils/auto-admin [pkgsrc-2020Q4] | | Portable tools for automating systems management |
devel/py-xopen [pkgsrc-2020Q4] | | Open compressed files transparently |
parallel/ganglia-monitor-core [pkgsrc-2020Q4] | | Ganglia cluster monitor, monitoring daemon |
biology/bwa [pkgsrc-2020Q4] | | Map low-divergent sequences against a large reference genome |
devel/R-rematch [pkgsrc-2020Q4] | | Match regular expressions with a nicer API |
biology/trimmomatic [pkgsrc-2020Q4] | | Flexible read trimming tool for Illumina NGS data |
biology/htslib [pkgsrc-2020Q4] | | C library for high-throughput sequencing data formats |
biology/vsearch [pkgsrc-2020Q4] | | Versatile open-source tool for metagenomics |
textproc/R-data.table [pkgsrc-2020Q4] | | Extension of data.frame |
textproc/man2html [pkgsrc-2020Q4] | | Convert nroff(1) man pages to HTML |
biology/bowtie2 [pkgsrc-2021Q1] | | Ultrafast, memory-efficient short read aligner |
biology/ad2vcf [pkgsrc-2021Q1] | | Add allelic depth info from a SAM stream to a VCF file |
archivers/libaec [pkgsrc-2021Q1] | | Adaptive entropy coding library |
biology/igv [pkgsrc-2021Q1] | | Visualization tool for genomic datasets |
biology/bcftools [pkgsrc-2021Q1] | | Tools for manipulating BCF and VCF variant call files |
biology/bedtools [pkgsrc-2021Q1] | | Swiss army knife for genome arithmetic |
biology/vcf-split [pkgsrc-2021Q1] | | Split a multi-sample VCF into single-sample VCFs |
biology/cdhit [pkgsrc-2021Q1] | | Clustering and comparing protein or nucleotide sequences |
biology/py-cutadapt [pkgsrc-2021Q1] | | Find and remove adapter sequences, primers, poly-A tails, etc |
devel/libctl [pkgsrc-2021Q1] | | Guile-based flexible control file library for scientific simulations |
biology/vcf2hap [pkgsrc-2021Q1] | | Generate .hap file from VCF for haplohseq |
biology/htslib [pkgsrc-2021Q1] | | C library for high-throughput sequencing data formats |
textproc/R-cellranger [pkgsrc-2021Q1] | | Translate spreadsheet cell ranges to rows and columns |
parallel/ganglia-monitor-core [pkgsrc-2021Q1] | | Ganglia cluster monitor, monitoring daemon |
biology/hisat2 [pkgsrc-2021Q1] | | Alignment program for mapping next-generation sequencing reads |
biology/fastqc [pkgsrc-2021Q1] | | Quality control tool for high throughput sequence data |
biology/stacks [pkgsrc-2021Q1] | | Software pipeline for building loci from short-read sequences |
devel/R-rematch [pkgsrc-2021Q1] | | Match regular expressions with a nicer API |
biology/samtools [pkgsrc-2021Q1] | | Tools for manipulating sequence alignment maps |
biology/canu [pkgsrc-2021Q1] | | Single molecule sequence assembler for genomes large and small |
devel/swig2 [pkgsrc-2021Q1] | | Simplified Wrapper and Interface Generator (version 2) |
math/udunits [pkgsrc-2021Q1] | | Library and program for manipulating units of physical quantities |
devel/py-xopen [pkgsrc-2021Q1] | | Open compressed files transparently |
textproc/man2html [pkgsrc-2021Q1] | | Convert nroff(1) man pages to HTML |
sysutils/auto-admin [pkgsrc-2021Q1] | | Portable tools for automating systems management |
textproc/R-data.table [pkgsrc-2021Q1] | | Extension of data.frame |
biology/generand [pkgsrc-2021Q1] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
security/munge [pkgsrc-2021Q1] | | Authentication service for creating and validating credentials |
biology/kallisto [pkgsrc-2021Q1] | | Quantify abundances of transcripts from RNA-Seq data |
biology/vsearch [pkgsrc-2021Q1] | | Versatile open-source tool for metagenomics |
biology/plink [pkgsrc-2021Q1] | | Whole-genome association analysis toolset |
parallel/slurm-wlm [pkgsrc-2021Q1] | | Simple Linux Utility for Resource Management |
biology/fastp [pkgsrc-2021Q1] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/py-dnaio [pkgsrc-2021Q1] | | Read and write FASTQ and FASTA files |
biology/biolibc [pkgsrc-2021Q1] | | Low-level high-performance bioinformatics library |
biology/bwa [pkgsrc-2021Q1] | | Map low-divergent sequences against a large reference genome |
biology/plinkseq [pkgsrc-2021Q1] | | C/C++ library for working with human genetic variation data |
biology/ncbi-blast+ [pkgsrc-2021Q1] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/trimmomatic [pkgsrc-2021Q1] | | Flexible read trimming tool for Illumina NGS data |
devel/R-rematch [pkgsrc-2021Q2] | | Match regular expressions with a nicer API |
security/munge [pkgsrc-2021Q2] | | Authentication service for creating and validating credentials |
devel/py-xopen [pkgsrc-2021Q2] | | Open compressed files transparently |
devel/libxtend [pkgsrc-2021Q2] | | Miscellaneous functions to extend libc |
biology/vsearch [pkgsrc-2021Q2] | | Versatile open-source tool for metagenomics |
biology/generand [pkgsrc-2021Q2] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/samtools [pkgsrc-2021Q2] | | Tools for manipulating sequence alignment maps |
biology/ad2vcf [pkgsrc-2021Q2] | | Add allelic depth info from a SAM stream to a VCF file |
biology/vcf-split [pkgsrc-2021Q2] | | Split a multi-sample VCF into single-sample VCFs |
biology/bowtie2 [pkgsrc-2021Q2] | | Ultrafast, memory-efficient short read aligner |
biology/vcf2hap [pkgsrc-2021Q2] | | Generate .hap file from VCF for haplohseq |
biology/trimmomatic [pkgsrc-2021Q2] | | Flexible read trimming tool for Illumina NGS data |
biology/py-dnaio [pkgsrc-2021Q2] | | Read and write FASTQ and FASTA files |
biology/plink [pkgsrc-2021Q2] | | Whole-genome association analysis toolset |
biology/peak-classifier [pkgsrc-2021Q2] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/igv [pkgsrc-2021Q2] | | Visualization tool for genomic datasets |
biology/fastqc [pkgsrc-2021Q2] | | Quality control tool for high throughput sequence data |
math/udunits [pkgsrc-2021Q2] | | Library and program for manipulating units of physical quantities |
biology/canu [pkgsrc-2021Q2] | | Single molecule sequence assembler for genomes large and small |
biology/bwa [pkgsrc-2021Q2] | | Map low-divergent sequences against a large reference genome |
biology/ncbi-blast+ [pkgsrc-2021Q2] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/py-cutadapt [pkgsrc-2021Q2] | | Find and remove adapter sequences, primers, poly-A tails, etc |
biology/fastp [pkgsrc-2021Q2] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/cdhit [pkgsrc-2021Q2] | | Clustering and comparing protein or nucleotide sequences |
devel/libctl [pkgsrc-2021Q2] | | Guile-based flexible control file library for scientific simulations |
textproc/R-cellranger [pkgsrc-2021Q2] | | Translate spreadsheet cell ranges to rows and columns |
archivers/libaec [pkgsrc-2021Q2] | | Adaptive entropy coding library |
biology/hisat2 [pkgsrc-2021Q2] | | Alignment program for mapping next-generation sequencing reads |
biology/bedtools [pkgsrc-2021Q2] | | Swiss army knife for genome arithmetic |
biology/biolibc [pkgsrc-2021Q2] | | Low-level high-performance bioinformatics library |
biology/stacks [pkgsrc-2021Q2] | | Software pipeline for building loci from short-read sequences |
biology/bcftools [pkgsrc-2021Q2] | | Tools for manipulating BCF and VCF variant call files |
biology/htslib [pkgsrc-2021Q2] | | C library for high-throughput sequencing data formats |
biology/plinkseq [pkgsrc-2021Q2] | | C/C++ library for working with human genetic variation data |
biology/kallisto [pkgsrc-2021Q2] | | Quantify abundances of transcripts from RNA-Seq data |
sysutils/auto-admin [pkgsrc-2021Q2] | | Portable tools for automating systems management |
parallel/slurm-wlm [pkgsrc-2021Q2] | | Simple Linux Utility for Resource Management |
parallel/ganglia-monitor-core [pkgsrc-2021Q2] | | Ganglia cluster monitor, monitoring daemon |
textproc/R-data.table [pkgsrc-2021Q2] | | Extension of data.frame |
devel/swig2 [pkgsrc-2021Q2] | | Simplified Wrapper and Interface Generator (version 2) |
textproc/man2html [pkgsrc-2021Q2] | | Convert nroff(1) man pages to HTML |
biology/trimmomatic [pkgsrc-2021Q3] | | Flexible read trimming tool for Illumina NGS data |
biology/biolibc [pkgsrc-2021Q3] | | Low-level high-performance bioinformatics library |
biology/cdhit [pkgsrc-2021Q3] | | Clustering and comparing protein or nucleotide sequences |
biology/htslib [pkgsrc-2021Q3] | | C library for high-throughput sequencing data formats |
biology/samtools [pkgsrc-2021Q3] | | Tools for manipulating sequence alignment maps |
biology/bowtie2 [pkgsrc-2021Q3] | | Ultrafast, memory-efficient short read aligner |
biology/biolibc-tools [pkgsrc-2021Q3] | | High-performance bioinformatics tools based on biolibc |
devel/libxtend [pkgsrc-2021Q3] | | Miscellaneous functions to extend libc |
biology/generand [pkgsrc-2021Q3] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/py-cutadapt [pkgsrc-2021Q3] | | Find and remove adapter sequences, primers, poly-A tails, etc |
sysutils/auto-admin [pkgsrc-2021Q3] | | Portable tools for automating systems management |
biology/vcf-split [pkgsrc-2021Q3] | | Split a multi-sample VCF into single-sample VCFs |
biology/peak-classifier [pkgsrc-2021Q3] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/bedtools [pkgsrc-2021Q3] | | Swiss army knife for genome arithmetic |
biology/plink [pkgsrc-2021Q3] | | Whole-genome association analysis toolset |
biology/fastqc [pkgsrc-2021Q3] | | Quality control tool for high throughput sequence data |
biology/bcftools [pkgsrc-2021Q3] | | Tools for manipulating BCF and VCF variant call files |
biology/bwa [pkgsrc-2021Q3] | | Map low-divergent sequences against a large reference genome |
archivers/libaec [pkgsrc-2021Q3] | | Adaptive entropy coding library |
biology/hisat2 [pkgsrc-2021Q3] | | Alignment program for mapping next-generation sequencing reads |
biology/plinkseq [pkgsrc-2021Q3] | | C/C++ library for working with human genetic variation data |
biology/fastp [pkgsrc-2021Q3] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/py-dnaio [pkgsrc-2021Q3] | | Read and write FASTQ and FASTA files |
biology/igv [pkgsrc-2021Q3] | | Visualization tool for genomic datasets |
biology/canu [pkgsrc-2021Q3] | | Single molecule sequence assembler for genomes large and small |
biology/ncbi-blast+ [pkgsrc-2021Q3] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/kallisto [pkgsrc-2021Q3] | | Quantify abundances of transcripts from RNA-Seq data |
devel/py-xopen [pkgsrc-2021Q3] | | Open compressed files transparently |
biology/vsearch [pkgsrc-2021Q3] | | Versatile open-source tool for metagenomics |
biology/stacks [pkgsrc-2021Q3] | | Software pipeline for building loci from short-read sequences |
biology/vcf2hap [pkgsrc-2021Q3] | | Generate .hap file from VCF for haplohseq |
biology/ad2vcf [pkgsrc-2021Q3] | | Add allelic depth info from a SAM stream to a VCF file |
biology/vcf-split [pkgsrc-2021Q4] | | Split a multi-sample VCF into single-sample VCFs |
biology/plinkseq [pkgsrc-2021Q4] | | C/C++ library for working with human genetic variation data |
biology/generand [pkgsrc-2021Q4] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/plink [pkgsrc-2021Q4] | | Whole-genome association analysis toolset |
biology/stacks [pkgsrc-2021Q4] | | Software pipeline for building loci from short-read sequences |
devel/py-xopen [pkgsrc-2021Q4] | | Open compressed files transparently |
devel/libxtend [pkgsrc-2021Q4] | | Miscellaneous functions to extend libc |
biology/bedtools [pkgsrc-2021Q4] | | Swiss army knife for genome arithmetic |
biology/kallisto [pkgsrc-2021Q4] | | Quantify abundances of transcripts from RNA-Seq data |
biology/biolibc [pkgsrc-2021Q4] | | Low-level high-performance bioinformatics library |
biology/fastqc [pkgsrc-2021Q4] | | Quality control tool for high throughput sequence data |
biology/vsearch [pkgsrc-2021Q4] | | Versatile open-source tool for metagenomics |
biology/bcftools [pkgsrc-2021Q4] | | Tools for manipulating BCF and VCF variant call files |
biology/cdhit [pkgsrc-2021Q4] | | Clustering and comparing protein or nucleotide sequences |
biology/ncbi-blast+ [pkgsrc-2021Q4] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/ad2vcf [pkgsrc-2021Q4] | | Add allelic depth info from a SAM stream to a VCF file |
biology/bwa [pkgsrc-2021Q4] | | Map low-divergent sequences against a large reference genome |
biology/biolibc-tools [pkgsrc-2021Q4] | | High-performance bioinformatics tools based on biolibc |
biology/trimmomatic [pkgsrc-2021Q4] | | Flexible read trimming tool for Illumina NGS data |
biology/samtools [pkgsrc-2021Q4] | | Tools for manipulating sequence alignment maps |
biology/peak-classifier [pkgsrc-2021Q4] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/vcf2hap [pkgsrc-2021Q4] | | Generate .hap file from VCF for haplohseq |
biology/bowtie2 [pkgsrc-2021Q4] | | Ultrafast, memory-efficient short read aligner |
sysutils/auto-admin [pkgsrc-2021Q4] | | Portable tools for automating systems management |
archivers/libaec [pkgsrc-2021Q4] | | Adaptive entropy coding library |
biology/py-dnaio [pkgsrc-2021Q4] | | Read and write FASTQ and FASTA files |
biology/hisat2 [pkgsrc-2021Q4] | | Alignment program for mapping next-generation sequencing reads |
biology/canu [pkgsrc-2021Q4] | | Single molecule sequence assembler for genomes large and small |
biology/fastp [pkgsrc-2021Q4] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/igv [pkgsrc-2021Q4] | | Visualization tool for genomic datasets |
biology/py-cutadapt [pkgsrc-2021Q4] | | Find and remove adapter sequences, primers, poly-A tails, etc |
biology/htslib [pkgsrc-2021Q4] | | C library for high-throughput sequencing data formats |
biology/bwa [pkgsrc-2022Q1] | | Map low-divergent sequences against a large reference genome |
biology/vsearch [pkgsrc-2022Q1] | | Versatile open-source tool for metagenomics |
biology/bedtools [pkgsrc-2022Q1] | | Swiss army knife for genome arithmetic |
biology/plink [pkgsrc-2022Q1] | | Whole-genome association analysis toolset |
biology/biolibc-tools [pkgsrc-2022Q1] | | High-performance bioinformatics tools based on biolibc |
biology/fastp [pkgsrc-2022Q1] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/plinkseq [pkgsrc-2022Q1] | | C/C++ library for working with human genetic variation data |
biology/hisat2 [pkgsrc-2022Q1] | | Alignment program for mapping next-generation sequencing reads |
biology/cdhit [pkgsrc-2022Q1] | | Clustering and comparing protein or nucleotide sequences |
biology/peak-classifier [pkgsrc-2022Q1] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/canu [pkgsrc-2022Q1] | | Single molecule sequence assembler for genomes large and small |
biology/igv [pkgsrc-2022Q1] | | Visualization tool for genomic datasets |
biology/vcf-split [pkgsrc-2022Q1] | | Split a multi-sample VCF into single-sample VCFs |
archivers/libaec [pkgsrc-2022Q1] | | Adaptive entropy coding library |
devel/libxtend [pkgsrc-2022Q1] | | Miscellaneous functions to extend libc |
biology/py-dnaio [pkgsrc-2022Q1] | | Read and write FASTQ and FASTA files |
biology/bowtie2 [pkgsrc-2022Q1] | | Ultrafast, memory-efficient short read aligner |
sysutils/auto-admin [pkgsrc-2022Q1] | | Portable tools for automating systems management |
biology/stacks [pkgsrc-2022Q1] | | Software pipeline for building loci from short-read sequences |
biology/vcf2hap [pkgsrc-2022Q1] | | Generate .hap file from VCF for haplohseq |
biology/trimmomatic [pkgsrc-2022Q1] | | Flexible read trimming tool for Illumina NGS data |
biology/py-cutadapt [pkgsrc-2022Q1] | | Find and remove adapter sequences, primers, poly-A tails, etc |
biology/kallisto [pkgsrc-2022Q1] | | Quantify abundances of transcripts from RNA-Seq data |
biology/samtools [pkgsrc-2022Q1] | | Tools for manipulating sequence alignment maps |
devel/py-xopen [pkgsrc-2022Q1] | | Open compressed files transparently |
biology/ncbi-blast+ [pkgsrc-2022Q1] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/bcftools [pkgsrc-2022Q1] | | Tools for manipulating BCF and VCF variant call files |
biology/biolibc [pkgsrc-2022Q1] | | Low-level high-performance bioinformatics library |
biology/ad2vcf [pkgsrc-2022Q1] | | Add allelic depth info from a SAM stream to a VCF file |
biology/htslib [pkgsrc-2022Q1] | | C library for high-throughput sequencing data formats |
biology/fastqc [pkgsrc-2022Q1] | | Quality control tool for high throughput sequence data |
biology/generand [pkgsrc-2022Q1] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/fastp [pkgsrc-2022Q2] | | Ultra-fast all-in-one FASTQ preprocessor |
math/basic-stats [pkgsrc-2022Q2] | | Command-line tool to perform basic statistics on tabular data |
devel/simde [pkgsrc-2022Q2] | | Header-only library for SIMD intrinsics |
biology/bowtie2 [pkgsrc-2022Q2] | | Ultrafast, memory-efficient short read aligner |
biology/htslib [pkgsrc-2022Q2] | | C library for high-throughput sequencing data formats |
biology/peak-classifier [pkgsrc-2022Q2] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/ncbi-blast+ [pkgsrc-2022Q2] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/canu [pkgsrc-2022Q2] | | Single molecule sequence assembler for genomes large and small |
biology/vcf2hap [pkgsrc-2022Q2] | | Generate .hap file from VCF for haplohseq |
biology/generand [pkgsrc-2022Q2] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/cdhit [pkgsrc-2022Q2] | | Clustering and comparing protein or nucleotide sequences |
biology/hisat2 [pkgsrc-2022Q2] | | Alignment program for mapping next-generation sequencing reads |
biology/igv [pkgsrc-2022Q2] | | Visualization tool for genomic datasets |
biology/fastx-toolkit [pkgsrc-2022Q2] | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
biology/bedtools [pkgsrc-2022Q2] | | Swiss army knife for genome arithmetic |
biology/biolibc-tools [pkgsrc-2022Q2] | | High-performance bioinformatics tools based on biolibc |
biology/kallisto [pkgsrc-2022Q2] | | Quantify abundances of transcripts from RNA-Seq data |
biology/plinkseq [pkgsrc-2022Q2] | | C/C++ library for working with human genetic variation data |
biology/ad2vcf [pkgsrc-2022Q2] | | Add allelic depth info from a SAM stream to a VCF file |
biology/vsearch [pkgsrc-2022Q2] | | Versatile open-source tool for metagenomics |
biology/trimmomatic [pkgsrc-2022Q2] | | Flexible read trimming tool for Illumina NGS data |
biology/bwa [pkgsrc-2022Q2] | | Map low-divergent sequences against a large reference genome |
biology/vcf-split [pkgsrc-2022Q2] | | Split a multi-sample VCF into single-sample VCFs |
devel/py-xopen [pkgsrc-2022Q2] | | Open compressed files transparently |
devel/libgtextutils [pkgsrc-2022Q2] | | Gordon text utilities |
biology/py-cutadapt [pkgsrc-2022Q2] | | Find and remove adapter sequences, primers, poly-A tails, etc |
biology/py-dnaio [pkgsrc-2022Q2] | | Read and write FASTQ and FASTA files |
biology/samtools [pkgsrc-2022Q2] | | Tools for manipulating sequence alignment maps |
biology/stacks [pkgsrc-2022Q2] | | Software pipeline for building loci from short-read sequences |
biology/bcftools [pkgsrc-2022Q2] | | Tools for manipulating BCF and VCF variant call files |
biology/biolibc [pkgsrc-2022Q2] | | Low-level high-performance bioinformatics library |
biology/fastqc [pkgsrc-2022Q2] | | Quality control tool for high throughput sequence data |
biology/plink [pkgsrc-2022Q2] | | Whole-genome association analysis toolset |
devel/libxtend [pkgsrc-2022Q2] | | Miscellaneous functions to extend libc |
archivers/libaec [pkgsrc-2022Q2] | | Adaptive entropy coding library |
sysutils/auto-admin [pkgsrc-2022Q2] | | Portable tools for automating systems management |
biology/stacks [pkgsrc-2022Q3] | | Software pipeline for building loci from short-read sequences |
devel/libxtend [pkgsrc-2022Q3] | | Miscellaneous functions to extend libc |
biology/fastx-toolkit [pkgsrc-2022Q3] | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
biology/biolibc [pkgsrc-2022Q3] | | Low-level high-performance bioinformatics library |
biology/trimmomatic [pkgsrc-2022Q3] | | Flexible read trimming tool for Illumina NGS data |
biology/vcf2hap [pkgsrc-2022Q3] | | Generate .hap file from VCF for haplohseq |
biology/biolibc-tools [pkgsrc-2022Q3] | | High-performance bioinformatics tools based on biolibc |
biology/generand [pkgsrc-2022Q3] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/ncbi-blast+ [pkgsrc-2022Q3] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/hisat2 [pkgsrc-2022Q3] | | Alignment program for mapping next-generation sequencing reads |
biology/vsearch [pkgsrc-2022Q3] | | Versatile open-source tool for metagenomics |
biology/samtools [pkgsrc-2022Q3] | | Tools for manipulating sequence alignment maps |
biology/bedtools [pkgsrc-2022Q3] | | Swiss army knife for genome arithmetic |
biology/igv [pkgsrc-2022Q3] | | Visualization tool for genomic datasets |
biology/plink [pkgsrc-2022Q3] | | Whole-genome association analysis toolset |
biology/ad2vcf [pkgsrc-2022Q3] | | Add allelic depth info from a SAM stream to a VCF file |
devel/libgtextutils [pkgsrc-2022Q3] | | Gordon text utilities |
devel/simde [pkgsrc-2022Q3] | | Header-only library for SIMD intrinsics |
devel/py-xopen [pkgsrc-2022Q3] | | Open compressed files transparently |
sysutils/auto-admin [pkgsrc-2022Q3] | | Portable tools for automating systems management |
archivers/libaec [pkgsrc-2022Q3] | | Adaptive entropy coding library |
biology/cdhit [pkgsrc-2022Q3] | | Clustering and comparing protein or nucleotide sequences |
biology/bcftools [pkgsrc-2022Q3] | | Tools for manipulating BCF and VCF variant call files |
biology/fastqc [pkgsrc-2022Q3] | | Quality control tool for high throughput sequence data |
biology/kallisto [pkgsrc-2022Q3] | | Quantify abundances of transcripts from RNA-Seq data |
biology/py-dnaio [pkgsrc-2022Q3] | | Read and write FASTQ and FASTA files |
biology/bowtie2 [pkgsrc-2022Q3] | | Ultrafast, memory-efficient short read aligner |
biology/canu [pkgsrc-2022Q3] | | Single molecule sequence assembler for genomes large and small |
biology/vcf-split [pkgsrc-2022Q3] | | Split a multi-sample VCF into single-sample VCFs |
biology/peak-classifier [pkgsrc-2022Q3] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/plinkseq [pkgsrc-2022Q3] | | C/C++ library for working with human genetic variation data |
biology/htslib [pkgsrc-2022Q3] | | C library for high-throughput sequencing data formats |
biology/bwa [pkgsrc-2022Q3] | | Map low-divergent sequences against a large reference genome |
biology/py-cutadapt [pkgsrc-2022Q3] | | Find and remove adapter sequences, primers, poly-A tails, etc |
math/basic-stats [pkgsrc-2022Q3] | | Command-line tool to perform basic statistics on tabular data |
biology/fastp [pkgsrc-2022Q3] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/fastp [pkgsrc-2022Q4] | | Ultra-fast all-in-one FASTQ preprocessor |
biology/biolibc [pkgsrc-2022Q4] | | Low-level high-performance bioinformatics library |
biology/vcf-split [pkgsrc-2022Q4] | | Split a multi-sample VCF into single-sample VCFs |
biology/trimmomatic [pkgsrc-2022Q4] | | Flexible read trimming tool for Illumina NGS data |
biology/fasda [pkgsrc-2022Q4] | | Fast and simple differential analysis |
biology/fastqc [pkgsrc-2022Q4] | | Quality control tool for high throughput sequence data |
devel/libxtend [pkgsrc-2022Q4] | | Miscellaneous functions to extend libc |
devel/simde [pkgsrc-2022Q4] | | Header-only library for SIMD intrinsics |
math/basic-stats [pkgsrc-2022Q4] | | Command-line tool to perform basic statistics on tabular data |
biology/cdhit [pkgsrc-2022Q4] | | Clustering and comparing protein or nucleotide sequences |
biology/canu [pkgsrc-2022Q4] | | Single molecule sequence assembler for genomes large and small |
biology/py-cutadapt [pkgsrc-2022Q4] | | Find and remove adapter sequences, primers, poly-A tails, etc |
archivers/libaec [pkgsrc-2022Q4] | | Adaptive entropy coding library |
sysutils/auto-admin [pkgsrc-2022Q4] | | Portable tools for automating systems management |
biology/fastq-trim [pkgsrc-2022Q4] | | Lightening fast sequence read trimmer |
biology/kallisto [pkgsrc-2022Q4] | | Quantify abundances of transcripts from RNA-Seq data |
biology/py-dnaio [pkgsrc-2022Q4] | | Read and write FASTQ and FASTA files |
biology/generand [pkgsrc-2022Q4] | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
biology/stacks [pkgsrc-2022Q4] | | Software pipeline for building loci from short-read sequences |
biology/ncbi-blast+ [pkgsrc-2022Q4] | | NCBI implementation of Basic Local Alignment Search Tool |
biology/bedtools [pkgsrc-2022Q4] | | Swiss army knife for genome arithmetic |
biology/hisat2 [pkgsrc-2022Q4] | | Alignment program for mapping next-generation sequencing reads |
biology/igv [pkgsrc-2022Q4] | | Visualization tool for genomic datasets |
biology/vsearch [pkgsrc-2022Q4] | | Versatile open-source tool for metagenomics |
devel/libgtextutils [pkgsrc-2022Q4] | | Gordon text utilities |
biology/gffread [pkgsrc-2022Q4] | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
biology/bcftools [pkgsrc-2022Q4] | | Tools for manipulating BCF and VCF variant call files |
biology/plinkseq [pkgsrc-2022Q4] | | C/C++ library for working with human genetic variation data |
biology/bowtie2 [pkgsrc-2022Q4] | | Ultrafast, memory-efficient short read aligner |
devel/py-xopen [pkgsrc-2022Q4] | | Open compressed files transparently |
biology/ad2vcf [pkgsrc-2022Q4] | | Add allelic depth info from a SAM stream to a VCF file |
biology/samtools [pkgsrc-2022Q4] | | Tools for manipulating sequence alignment maps |
biology/bwa [pkgsrc-2022Q4] | | Map low-divergent sequences against a large reference genome |
biology/vcf2hap [pkgsrc-2022Q4] | | Generate .hap file from VCF for haplohseq |
biology/rna-seq [pkgsrc-2022Q4] | | Core tools needed for RNA-Seq analysis |
biology/biolibc-tools [pkgsrc-2022Q4] | | High-performance bioinformatics tools based on biolibc |
biology/plink [pkgsrc-2022Q4] | | Whole-genome association analysis toolset |
biology/peak-classifier [pkgsrc-2022Q4] | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
biology/htslib [pkgsrc-2022Q4] | | C library for high-throughput sequencing data formats |
biology/fastx-toolkit [pkgsrc-2022Q4] | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |