tool for aligning cDNA and genomic DNA
batch spliced alignment of cDNA sequences to a target genome
comparative metagenomics method dedicated to NGS datasets
approximate comparative metagenomics method dedicated to NGS datasets
simulation model for breast/lung cancer risk
astronomical image processing tool
architecture-independent files for siril
Split Kmer Analysis
strategic Kmer extension for scrupulous assemblies
post-processing of high-throughput DNA sequence reads
Image visualization and access to catalogs and data for astronomy
produce plots and drawings through Xfig's fig2dev in S-Lang
Sequence Mapping and Alignment Tool
Sequence Mapping and Alignment Tool (examples)
determine similar regions between two strings or genomic sequences
software suite for single molecule, real-time sequencing
location of genes from DNA sequence with hidden markov model
Scalable Nucleotide Alignment Program
structural variation caller using third-generation sequencing
rapid haploid variant calling and core genome alignment
rapid haploid variant calling and core genome alignment (examples)
fast, stringent short-read mapping software
Binary code for the package snp-sites
aligner of short reads of next generation sequencers
short-read assembly method to build de novo draft assembly
resequencing utility that can assemble consensus sequence of genomes
tool for filtering, mapping and OTU-picking NGS reads
Source extractor for astronomical images
Estimating the quality of a source of entropy
alignment-free sequence comparison using spaced words
genome assembler for single-cell and isolates data sets
splicing-aware transcript-alignment to genomic DNA
splicing-aware transcript-alignment to genomic DNA (data)
automated theorem prover for first-order logic with equality
Geospatial extension for SQLite - tools
Synchrotron image corrections and azimuthal integration
Visualisation tool for Smoothed Particle Hydrodynamics simulation
SIMD partial order alignment tool
single-pass sequencing read accuracy improver
analyze and visualize phylogeographic reconstructions
Spectrum Viewer
utilities for the NCBI Sequence Read Archive
Short Read Sequence Typing for Bacterial Pathogens
genomics application for assembling millions of very short DNA sequences
example data for SSAKE, a genomic assembler of short reads
scaffolding pre-assembled contigs after extension
stupid simple (ba)sh testing
Smith-Waterman aligner based on libssw
pipeline for building loci from short-read DNA sequences