GMOD / GBrowseLinks
the Generic Genome Browser
☆49Updated 2 years ago
Alternatives and similar repositories for GBrowse
Users that are interested in GBrowse are comparing it to the libraries listed below
Sorting:
- Phylogenetic analysis of multi-species genome sequence alignments to identify conserved protein-coding regions☆69Updated 2 years ago
- Maximum likelihood demultiplexing☆48Updated 9 months ago
- De novo transcriptome assembler for short reads☆64Updated 7 years ago
- CoGe (Comparative Genomics) Platform☆46Updated 3 years ago
- Calculates the lowest common ancestors of each query sequence in a Blast result☆31Updated 8 years ago
- Miscellaneous Bioinformatics scripts etc mostly in Python☆45Updated 2 weeks ago
- KOBAS: a command line tool for identifying significant pathways from genomic data☆32Updated 15 years ago
- ☆63Updated 4 years ago
- Converting and demultiplexing of PacBio BAM files into gzipped fasta and fastq files.☆39Updated 2 years ago
- A collection of scripts developed to interact with fasta, fastq and sam/bam files.☆53Updated 9 years ago
- Tools for querying and analysis of genomic data☆27Updated 3 weeks ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆58Updated 8 years ago
- Assembly by Reduced Complexity (ARC)☆42Updated 9 years ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆41Updated 6 years ago
- Automatically exported from code.google.com/p/prottest3☆38Updated 7 years ago
- A 3'-end adapter contaminant trimmer☆95Updated 7 years ago
- transXpress: a Snakemake pipeline for streamlined de novo transcriptome assembly and annotation☆27Updated last year
- Error correction for Illumina RNA-seq reads☆67Updated last year
- A snakemake pipeline for SV analysis from nanopore genome sequencing☆52Updated 5 years ago
- PacBio hybrid error correction through iterative short read consensus☆60Updated 6 years ago
- A reference viral database (RVDB)☆26Updated 6 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 3 years ago
- An illumina paired-end and mate-pair short read simulator. This project attempts to model as many of the quirks that exist in Illumina da…☆67Updated 11 years ago
- Algorithms to compute DNA complexity☆34Updated 3 years ago
- Generate unique KMERs for every contig in a FASTA file☆48Updated 3 years ago
- Visualize whole genome alignments as linear maps☆73Updated 3 months ago
- Code for nanopore paper☆33Updated 10 years ago
- OPAL: Open-community Profiling Assessment tooL☆29Updated 10 months ago
- My collection of light bioinformatics analysis pipelines for specific tasks☆76Updated last year
- Tools for bam file processing☆55Updated 10 years ago