evoldoers / machineboss
Bioinformatics Open Source Sequence machine
☆33Updated last year
Alternatives and similar repositories for machineboss:
Users that are interested in machineboss are comparing it to the libraries listed below
- Annotating principal splice isoforms☆14Updated 4 months ago
- The software involved in the MetaPhase project, as described in G3 (http://dx.doi.org/10.1534/g3.114.011825)☆16Updated 6 years ago
- Malleable All-seeing Journal Of Research Artifacts☆36Updated last year
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- Classify sequencing reads using MinHash.☆48Updated 4 years ago
- ☆19Updated 7 years ago
- Small general purpose library for C and Python with focus on bioinformatics.☆29Updated 2 years ago
- Ampseer examines reads in fastq format and identifies which multiplex PCR primer set was used to generate the SARS-CoV-2 sequencing libra…☆14Updated last year
- REINDEER REad Index for abuNDancE quERy☆57Updated 7 months ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 5 years ago
- Whole Exome/Whole Genome Sequencing alignment pipeline☆28Updated 5 months ago
- k-mer similarity analysis pipeline☆20Updated last month
- ☆23Updated 5 years ago
- exploring viral genome assembly with variation graph tools☆19Updated 4 years ago
- Symmetric DUST for finding low-complexity regions in DNA sequences☆36Updated last year
- Novel Adjacency Identification with Barcoded Reads☆13Updated 2 years ago
- ☆28Updated 8 months ago
- overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites☆33Updated last week
- reference free variant assembly☆33Updated last year
- Reference Phylogeny for Bacterial and Archaeal Genomes☆25Updated 2 years ago
- Find Unique genomic Regions☆29Updated last month
- Generate random test data for bioinformatics☆25Updated 8 months ago
- Benchmark datasets for WGS analysis☆37Updated 5 years ago
- URMAP ultra-fast read mapper☆38Updated 4 years ago
- ☆21Updated last year
- VIRULIGN: fast codon-correct alignment and annotation of viral genomes☆33Updated 3 years ago
- Build sourmash databases for genbank.☆12Updated last year
- PhyloCSF++ computes PhyloCSF tracks for whole-genome multiple sequence alignments, scores single MSA, annotates CDS features in GFF/GTF f…☆30Updated 3 years ago
- Accurate Typing of Human Leukocyte Antigen (HLA) by Oxford Nanopore Sequencing☆15Updated 7 years ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆47Updated 6 years ago