dariober / ASCIIGenomeLinks
Text Only Genome Viewer!
☆229Updated 5 months ago
Alternatives and similar repositories for ASCIIGenome
Users that are interested in ASCIIGenome are comparing it to the libraries listed below
Sorting:
- A tool set for short variant discovery in genetic sequence data.☆202Updated 4 years ago
- Variant calling and somatic mutation/CNV detection for next-generation sequencing data☆165Updated 2 years ago
- BEDOPS: high-performance genomic feature operations☆354Updated 6 months ago
- Web application to explore the Sequence Read Archive.☆217Updated 4 months ago
- A fast Python and command-line utility for extracting simple statistics against genome positions based on sequence alignments from a SAM …☆194Updated 3 weeks ago
- An efficient FASTQ manipulation suite☆138Updated 5 years ago
- Bayesian haplotype-based mutation calling☆320Updated last month
- samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.☆235Updated 4 years ago
- Count bases in BAM/CRAM files☆319Updated 3 years ago
- VarDict☆200Updated last year
- genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF☆144Updated 4 months ago
- Windowed Adaptive Trimming for fastq files using quality☆226Updated 8 years ago
- annotate a VCF with other VCFs/BEDs/tabixed files☆389Updated 2 months ago
- Read trimming tool for Illumina NGS data.☆147Updated 10 years ago
- RTG Tools: Utilities for accurate VCF comparison and manipulation☆328Updated 5 months ago
- UCSC command line bioinformatic utilities☆185Updated last year
- Simple test framework for Nextflow pipelines☆173Updated 2 weeks ago
- classify, merge, tracking and annotation of GFF files by comparing to a reference annotation GFF☆250Updated 4 months ago
- Tool for stripping adaptors and/or merging paired reads with overlap into single reads.☆145Updated 9 years ago
- tools for adding mutations to existing .bam files, used for testing mutation callers☆248Updated last year
- Reads simulator☆282Updated 4 years ago
- GRIDSS: the Genomic Rearrangement IDentification Software Suite☆280Updated 6 months ago
- Documentation and description of AWS iGenomes S3 resource.☆117Updated 11 months ago
- GATK RNA-Seq Variant Calling in Nextflow☆137Updated 2 years ago
- Biopieces is a bioinformatic framework of tools easily used and easily created.☆144Updated 7 years ago
- miscellaneous scripts for bioinformatics/genomics that dont merit their own repo.☆182Updated 6 years ago
- ABRA2☆95Updated 2 years ago
- This repository contains chromosome/contig name mappings between UCSC <-> Ensembl <-> Gencode for a variety of genomes.☆244Updated 2 years ago
- a toolkit for working with Oxford nanopore data☆245Updated 2 years ago
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆128Updated 5 years ago