ericminikel / cureffiLinks
CureFFI.org
☆16Updated 4 months ago
Alternatives and similar repositories for cureffi
Users that are interested in cureffi are comparing it to the libraries listed below
Sorting:
- Convert genetic variants to minimal representation☆23Updated 8 years ago
- Blacktie: a streamlined interface to the popular tophat/cufflinks RNA-seq pipeline☆26Updated 10 years ago
- The JunctionSeq R package is a powerful tool for testing and visualizing differential usage of exons and splice junctions in next-generat…☆29Updated 8 years ago
- A talk on Makesfiles in bioinformatics☆26Updated 12 years ago
- Useful FILe and stream Operations☆45Updated 10 years ago
- Mapping of GENCODE gene annotation set files to older assembies☆13Updated 2 years ago
- A tool for evaluating RNA seq mapping☆22Updated 6 years ago
- Allele frequency filter app☆14Updated 3 years ago
- Natural Language Search and Analysis of High Dimensional Genomic Data☆48Updated 6 months ago
- Allele frequency filtering for Mendelian variant discovery☆18Updated 9 years ago
- Gene lists related to cancer immunotherapy☆14Updated last year
- Quantitative Allele Specific Analysis of Reads. Joint genotyping & ASE inference for RNA-seq data☆27Updated 9 years ago
- Fast fusion detection using kallisto☆79Updated 8 months ago
- ☆37Updated 3 years ago
- A software for the multispecies design of CRISPR/Cas9 libraries☆36Updated 3 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- ☆28Updated 8 years ago
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 9 years ago
- Genomic VCF to tab-separated values☆48Updated 2 years ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆41Updated 7 years ago
- Sample Level Analysis of Pathway Alteration Enrichments☆10Updated 7 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- ☆21Updated 4 years ago
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆71Updated 2 years ago
- 📊Evaluating, filtering, comparing, and visualising VCF☆28Updated 2 years ago
- Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently☆59Updated 2 years ago
- Finding cryptic relationships to boost disease gene detection☆12Updated 2 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 8 years ago
- An approximate sequence pattern matcher for FASTQ/FASTA files.☆32Updated 10 years ago