ialbert / genescape-central
Gene Ontology subgraph visualizations
☆19Updated 8 months ago
Alternatives and similar repositories for genescape-central
Users that are interested in genescape-central are comparing it to the libraries listed below
Sorting:
- Nanopore Real-Time Analysis Tool☆15Updated 8 months ago
- This is a read-only mirror of the CRAN R package repository. chromoMap — Interactive Genomic Visualization of Biological Data☆9Updated 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
- fastest GTF/GFF-to-BED converter chilling around☆25Updated 3 months ago
- ☆16Updated last year
- A command line tool to compute mapping statistics from a BAM file☆24Updated 3 years ago
- ☆31Updated 11 months ago
- ☆16Updated last year
- SAMStat displays various properties of next-generation sequencing reads stored in SAM/BAM format.☆24Updated last year
- Distribution of TEs and their relationship to genes in host genome☆22Updated last year
- Chromatin ACcessibility and Transcriptomics Unifying Software☆16Updated 6 months ago
- Rapid and accurate ancestry inference using SNVs.☆19Updated last month
- Nextflow pipeline that runs DESeq2 on data processed with the nextflow RNAseq pipeline☆12Updated 11 months ago
- Efficient retrieval, download, and unification of genomic data from leading biodiversity databases☆15Updated this week
- Structural variant (SV) analysis tools☆36Updated 10 months ago
- CNV Rapid Aberration Detection And Reporting☆12Updated 4 years ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated last month
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- MapCaller – An efficient and versatile approach for short-read alignment and variant detection in high-throughput sequenced genomes☆30Updated 4 years ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆35Updated 10 months ago
- Two pass alignment for long reads☆22Updated 4 years ago
- Fast long-read mapper and whole-genome aligner (accelerated version of minimap2)☆31Updated last week
- DNA multiple sequence aligner, official version from Penn State's Miller Lab☆32Updated 6 years ago
- ☆15Updated 6 years ago
- Quality assessment of de novo transcriptome assemblies from RNA-Seq data☆21Updated 6 months ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 2 months ago
- A pipeline for the identification of Compound Heterozygous Variants☆9Updated 2 years ago
- fastq quality assessment and filtering tool☆18Updated 2 years ago
- A tool to extract LOH blocks from VCF, BAM and FASTA data☆21Updated 8 months ago
- ☆14Updated 7 years ago