wurmlab / sequenceserverLinks
Intuitive graphical web interface for running BLAST bioinformatics tool (i.e. have your own custom NCBI BLAST site!)
☆295Updated 2 months ago
Alternatives and similar repositories for sequenceserver
Users that are interested in sequenceserver are comparing it to the libraries listed below
Sorting:
- Genome annotation with AUGUSTUS☆324Updated 5 months ago
- ☆300Updated last month
- Short read de novo assembler using de Bruijn graphs, as published in: D.R. Zerbino and E. Birney. 2008. Velvet: algorithms for de novo sh…☆293Updated 3 months ago
- GFF/GTF utility providing format conversions, region filtering, FASTA sequence extraction and more☆451Updated last year
- Next generation sequencing reads de novo assembler.☆239Updated 4 months ago
- TransDecoder source☆301Updated 4 months ago
- Read trimming tool for Illumina NGS data.☆149Updated 10 years ago
- Fast genome and metagenome distance estimation using MinHash☆431Updated 4 months ago
- Count bases in BAM/CRAM files☆323Updated 3 years ago
- HyPhy: Hypothesis testing using Phylogenies☆249Updated this week
- A genome browser designed for complex structural variants and long reads.☆296Updated 7 months ago
- (Not Offical) BBMap short read aligner, and other bioinformatic tools.☆244Updated 4 years ago
- GFF and GVF specification documents☆219Updated last year
- Program for aligning DNA sequences, a pairwise aligner.☆239Updated 7 months ago
- C++ API & command-line toolkit for working with BAM data☆429Updated 8 months ago
- Genome-scale protein function classification☆363Updated last week
- GFF and GTF file manipulation and interconversion☆312Updated last week
- Eukaryotic Genome Annotation Pipeline☆378Updated last week
- UCSC Genome Browser source. "beta" is released version / "master" is testing.☆250Updated last week
- FASTA/FASTQ pre-processing programs☆197Updated 3 years ago
- DELLY2: Structural variant discovery by integrated paired-end and split-read analysis☆505Updated 2 months ago
- Pilon is an automated genome assembly improvement and variant detection tool☆374Updated 3 years ago
- PAired-eND Assembler for DNA sequences☆137Updated 5 years ago
- BEDOPS: high-performance genomic feature operations☆357Updated 9 months ago
- annotate a VCF with other VCFs/BEDs/tabixed files☆395Updated 4 months ago
- Fast and frugal disk based k-mer counter☆323Updated 2 weeks ago
- a toolkit for working with Oxford nanopore data☆243Updated 2 years ago
- ☆347Updated 10 months ago
- NCBI Prokaryotic Genome Annotation Pipeline☆364Updated 2 months ago
- Windowed Adaptive Trimming for fastq files using quality☆226Updated 8 years ago