ImperialCardioGenetics / uORFsLinks
☆18Updated 5 years ago
Alternatives and similar repositories for uORFs
Users that are interested in uORFs are comparing it to the libraries listed below
Sorting:
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- FermiKit small variant calls for public SGDP samples☆17Updated 8 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Updated 5 years ago
- ☆25Updated last year
- Comprehensive Human Expressed SequenceS☆17Updated 10 months ago
- ☆20Updated last year
- ☆21Updated last month
- BigWig manpulation tools using libBigWig and htslib☆29Updated 9 months ago
- Aggregation and analyses of rare CNVs across diseases☆14Updated 2 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- Personal diploid genome creation and coordinate conversion☆26Updated 2 months ago
- alternative splicing analysis pipeline☆19Updated 4 years ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Updated last year
- Introme prioritises coding and noncoding splice-altering variants for clinical variant interpretation☆21Updated 2 months ago
- ☆22Updated last month
- ☆9Updated 8 years ago
- Long read to rMATS☆31Updated 2 years ago
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Updated 7 years ago
- a set of NGS pipelines☆24Updated last week
- Copy Number Methods for Detection and Genome Wide Association Tests☆22Updated 7 months ago
- Sample Contamination Estimate from VCF☆19Updated 7 months ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆40Updated 6 years ago
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆23Updated 4 years ago
- interactive plots for differential expression analysis☆32Updated 2 months ago
- fast webservices based query tool for large sets of genomic features☆25Updated 3 weeks ago
- uORF-Tools are a workflow and a collection of tools for the analysis of 'Upstream Open Reading Frames' (short uORFs)☆13Updated 5 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆24Updated 9 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago