atgu / aou_gwasLinks
☆12Updated 3 weeks ago
Alternatives and similar repositories for aou_gwas
Users that are interested in aou_gwas are comparing it to the libraries listed below
Sorting:
- RNA-seq data comprehensive data analysis toolbox☆19Updated 3 years ago
- ☆16Updated 2 years ago
- Lollipop-diagram to interactively visualize genetic mutations☆33Updated last year
- RNA-seq for Mendelian disease diagnostics: A hands-on tutorial through bioinformatic tools and workflows☆17Updated 3 years ago
- VarGen is an R package designed to get a list of variants related to a disease. It just need an OMIM morbid ID as input and optionally a…☆17Updated last year
- Allele frequency filter app☆14Updated 3 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆35Updated 4 years ago
- Suite of heritability and genetic correlation estimation tools for exome-sequencing data☆34Updated 8 months ago
- Simulation of rare and common variants based on 1000 genomes data☆19Updated 4 years ago
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆40Updated last year
- A Practical (And Opinionated) Guide To Analyzing 450K Data☆35Updated 11 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Toolkit for QTL mapping and meta-analysis.☆17Updated 3 years ago
- R package enabling statistical association analysis and using immunogenetic data transformation functions for HLA amino acid fine mapping…☆14Updated last year
- Interactive eQTL visualizations☆13Updated 2 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Updated 9 years ago
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R☆32Updated last month
- ☆12Updated 3 years ago
- A small R package to make sequencing read coverage plots in R.☆39Updated 2 weeks ago
- R package for extracting mutation signatures from a list of somatic mutations☆37Updated 6 years ago
- Scripts and software supplement for "Gene-level differential analysis at transcript-level resolution" by Yi, Pimentel, Bray and Pachter☆19Updated 7 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- ALOFT, the Annotation Of Loss-of-Function Transcripts, provides extensive functional annotations to loss-of-function variants in the hum…☆19Updated 5 years ago
- methylR: a single shiny solution from sequencer data to pathway analysis☆12Updated last year
- Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer☆21Updated 4 years ago
- Calculate and plot distributions of genomic ranges☆26Updated 6 months ago
- Rapid and accurate ancestry inference using SNVs.☆26Updated 2 months ago
- Assembly of RNA reads to determine the effect of a cancer mutation on protein sequence☆25Updated last year