signalbash / borfLinks
ORF prediction using python
☆12Updated 4 years ago
Alternatives and similar repositories for borf
Users that are interested in borf are comparing it to the libraries listed below
Sorting:
- DETONATE: DE novo TranscriptOme rNa-seq Assembly with or without the Truth Evaluation☆14Updated 9 years ago
- ☆28Updated 3 years ago
- Converting and demultiplexing of PacBio BAM files into gzipped fasta and fastq files.☆39Updated 2 years ago
- Trimming tool for Oxford Nanopore sequence data☆22Updated 4 years ago
- Find Unique genomic Regions☆32Updated last month
- Whole organelle genome-wide alignment construction method, which ultilizes BLAST tool, to facilitate phylogeny analysis☆11Updated 7 years ago
- The final version 2 release of our software to detect core genes in eukaryotic genomes☆29Updated 10 years ago
- ☆29Updated 4 years ago
- Database-Integrated Genome Screening (DIGS) tool. Explore the dark genome using BLAST and a relational database.☆11Updated last year
- BItsliced Genomic Signature Index - Efficient indexing and search in very large collections of WGS data☆10Updated 2 years ago
- SAMStat displays various properties of next-generation sequencing reads stored in SAM/BAM format.☆24Updated 2 years ago
- ☆17Updated 5 months ago
- Perl and Python scripts allowing to get sequence information from GenBank, RefSeq or ENA sequence repositories☆14Updated 8 months ago
- Consensus genome annotation using OMA☆29Updated 5 months ago
- Read nanopore sequence reads in real-time☆14Updated 8 years ago
- cgat-apps repository☆34Updated 8 months ago
- ☆21Updated 6 years ago
- transposable element typing pipeline☆19Updated last year
- easy_sbatch - Batch submitting Slurm jobs with script templates☆16Updated 3 years ago
- Generate unique KMERs for every contig in a FASTA file☆48Updated 3 years ago
- PhyloCSF++ computes PhyloCSF tracks for whole-genome multiple sequence alignments, scores single MSA, annotates CDS features in GFF/GTF f…☆31Updated 3 years ago
- Utility program for extracting sequences from a fasta/fastq file☆35Updated 11 months ago
- In-depth characterization and annotation of differences between two sets of DNA sequences☆63Updated 5 years ago
- profile the repeat landscape in a genome☆16Updated 11 years ago
- finding conserved regions in highly diverse genomes☆15Updated 6 months ago
- Haplotype-aware genome assembly toolkit☆30Updated 5 years ago
- Integrated toolkit for analysis and evaluation of annotated genomes☆25Updated 4 months ago
- Perl scripts for working with the GFF format☆16Updated 14 years ago
- Gap2Seq is a gap filling and insertion genotyping tool.☆22Updated last year
- Fast in-silico normalization algorithm for NGS data☆23Updated 4 years ago