pre-filter for the counting of very large collections of nucleotide sequences
pre-filter for querying very large collections of nucleotide sequences
cross-platform and ultrafast toolkit for FASTA/Q file manipulation
examples for seqkit: toolkit for FASTA/Q file manipulation
imagemagick-like frontend to Biopython SeqIO
stripping adaptors and/or merging paired reads of DNA sequences with overlap
example data set for seqprep - only used for testing
Salmonella serotyping from genome sequencing data
Fast and lightweight tool for processing sequences in the FASTA or FASTQ format
finds a suitable linear order for a set of objects
test data for seriation
de novo genome assembler that uses string graphs
fast and accurate method for estimation of haplotypes (phasing)
nanopore whole genome assembly (binaries and scripts)
graphical user interface for SHELXL
put Shiny web apps online
Assemble bacterial isolate genomes from Illumina paired-end reads
Test Data for shovill
comparative genomics tool
comparative genomics tool (example data)
align expressed RNA sequences on a DNA template
windowed adaptive trimming tool for FASTQ files using quality
Simple greedy multiple alignment of non-coding DNA sequences
GUI viewer for biosignals such as EEG, EMG, and ECG
Toolbox for X-Ray data analysis - Executables
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)
command line tools to handle SMILES descriptors
determine similar regions between two strings or genomic sequences
software suite for single molecule, real-time sequencing
pythonic workflow management system
location of genes from DNA sequence with hidden markov model
Scalable Nucleotide Alignment Program
structural variation caller using third-generation sequencing
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