biology - The NetBSD Packages Collection
Software for the biological sciences
There are
73
packages in this category:
- R-popbio-2.7
- Construction and Analysis of Matrix Population Models
- ad2vcf-0.1.6
- Add allelic depth info from a SAM stream to a VCF file
- arka-0.11nb2
- Graphic interface for the programs from the GP package
- azara-2.7nb10
- Programs to process and view NMR data
- bcftools-1.15nb2
- Tools for manipulating BCF and VCF variant call files
- beagle-5.2
- Phasing genotypes and imputing ungenotyped markers
- bedtools-2.30.0nb1
- Swiss army knife for genome arithmetic
- biolibc-0.2.3
- Low-level high-performance bioinformatics library
- biolibc-tools-0.1.3
- High-performance bioinformatics tools based on biolibc
- bioperl-1.7.7nb3
- Perl tools for computational molecular biology
- bodr-9nb17
- Blue Obelisk Data Repository
- bowtie2-2.4.4nb2
- Ultrafast, memory-efficient short read aligner
- bwa-0.7.17nb6
- Map low-divergent sequences against a large reference genome
- canu-1.8nb13
- Single molecule sequence assembler for genomes large and small
- cdhit-4.8.1nb1
- Clustering and comparing protein or nucleotide sequences
- chemical-mime-data-0.1.94
- Chemical mime and file type support for desktops
- chemtool-1.6.14nb16
- Program for drawing organic molecules
- clustalw-2.1
- General purpose multiple alignment program for DNA or proteins
- coalesce-1.5.0.2nb1
- Estimates effective population size and mutation rate
- coordgenlibs-1.4.2nb4
- 2D coordinate generation for molecules
- fastDNAml-1.2.2
- Program derived from Joseph Felsenstein's version 3.3 DNAML
- fastp-0.20.0
- Ultra-fast all-in-one FASTQ preprocessor
- fastqc-0.11.9nb2
- Quality control tool for high throughput sequence data
- fastx-toolkit-0.0.14.6nb1
- CLI tools for Short-Reads FASTA/FASTQ files preprocessing
- filter-fastq-0.0.0.20210527nb1
- Filter reads from a FASTQ file
- fluctuate-1.4
- Estimation of population growth rate
- gabedit-2.4.8nb12
- Graphical User Interface to computational chemistry packages
- generand-0.1.2
- Generate random genomic data in FASTA/FASTQ, SAM, or VCF format
- genesplicer-20030403
- Computational Method for Splice Site Prediction
- glimmer-2.13nb1
- System for finding genes in microbial DNA
- gnome-chemistry-utils-0.14.16nb10
- GChemPaint, a 2D chemical editor and other programs
- gp-0.26
- Manipulate DNA/RNA sequence in a Unix fashion
- gromacs-4.5.5nb17
- Molecular dynamics package
- hisat2-2.2.1nb2
- Alignment program for mapping next-generation sequencing reads
- hmmer-3.0
- Implementation of profile HMM software for protein sequence analysis
- htslib-1.15.1
- C library for high-throughput sequencing data formats
- igv-2.9.2
- Visualization tool for genomic datasets
- kallisto-0.48.0
- Quantify abundances of transcripts from RNA-Seq data
- lucy-1.20
- Sequence Cleanup Program
- maeparser-1.2.4nb4
- Parser for Maestro file format
- miniasm-0.3
- OLC-based de novo assembler for long reads
- minimap2-2.24
- Sequence alignment program for noisy, long reads
- molsketch-0.7.2nb3
- Program for drawing molecular structures
- mopac-7.0nb1
- Molecular energy calculation program
- mpqc-2.3.1nb12
- The Massively Parallel Quantum Chemistry Program
- mummer-3.20nb10
- System for aligning whole genome sequences
- ncbi-blast+-2.13.0nb3
- NCBI implementation of Basic Local Alignment Search Tool
- nut-15.8
- Record what you eat and analyze your meals
- openbabel-3.1.1nb11
- Chemistry file translation program
- p5-Bio-ASN1-EntrezGene-1.73nb2
- Regular expression-based Perl Parser for NCBI Entrez Gene
- pdbalign-20030812
- Prediction of Protein Secondary Structure and Active Sites
- peak-classifier-0.1.4nb1
- Classify ChIP/ATAC-Seq peaks based on features provided in a GFF
- phylip-3.69
- Phylogeny Inference Package
- plink-1.07nb1
- Whole-genome association analysis toolset
- plinkseq-0.08nb6
- C/C++ library for working with human genetic variation data
- primer3-2.3.6
- Design PCR primers
- profit-2.2nb1
- Performs least squares fits of two protein structures
- puzzle-5.2
- Maximum likelihood analysis of molecular sequence data
- py310-biopython-1.79
- Python libraries for computational molecular biology
- py310-cutadapt-3.5
- Find and remove adapter sequences, primers, poly-A tails, etc
- py310-dnaio-0.5.1nb1
- Read and write FASTQ and FASTA files
- py310-pydicom-2.2.2nb2
- Pure python package for working with DICOM files
- racon-1.4.3
- Genomic consensus builder
- rasmol-2.7.3nb2
- Molecular Graphics Visualisation Tool
- samtools-1.15nb2
- Tools for manipulating sequence alignment maps
- sewer-2.6nb2
- SEquence Analysis using WEb Resources
- stacks-2.60nb2
- Software pipeline for building loci from short-read sequences
- stride-20030804
- Protein secondary structure assignment from atomic coordinates
- Trimmomatic-0.38
- Flexible read trimming tool for Illumina NGS data
- vcf-split-0.1.5
- Split a multi-sample VCF into single-sample VCFs
- vcf2hap-0.1.6
- Generate .hap file from VCF for haplohseq
- vsearch-2.18.0
- Versatile open-source tool for metagenomics
- xylem-1.8.7
- Tools for manipulation of genetic databases