omerwe / LEAPLinks
Liability Estimation for Case-Control Studies
☆10Updated 5 years ago
Alternatives and similar repositories for LEAP
Users that are interested in LEAP are comparing it to the libraries listed below
Sorting:
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆31Updated 8 years ago
- Hotspot is a program for identifying genomic regions of local enrichment of short-read sequence tags.☆16Updated 11 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- ☆20Updated 8 years ago
- A tool for Read Multi-Mapper Resolution☆24Updated 8 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 6 years ago
- python wrapper to dpryan79's bigwig library using cffi☆19Updated 9 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- ☆21Updated 8 years ago
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 9 years ago
- Library and command line scripts for fitting heteroskedastic linear mixed models to genetic data. Can be used to perform GWAS for genetic…☆18Updated 7 years ago
- A framework for network analysis and display of SNPs☆19Updated 9 years ago
- An R package for detecting Gene-by-Environment (GxE) interaction effects on the transcriptome using Allele Specific Expression quantified…☆21Updated 4 years ago
- Code to reproduce analyses from the sleuth paper☆16Updated 6 years ago
- ☆43Updated 9 years ago
- Efficient handling of FASTQ files from Python☆51Updated 3 months ago
- ALOFT, the Annotation Of Loss-of-Function Transcripts, provides extensive functional annotations to loss-of-function variants in the hum…☆19Updated 6 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- User-friendly Bioinformatics Tools☆18Updated 4 years ago
- Enriched Domain Detector for ChIP-seq data☆16Updated 3 years ago
- 7C: Computational Chromosome Conformation Capture by Correlation of ChIP-seq at CTCF motifs☆13Updated 2 weeks ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- Tools for handling HiC and 5C data☆24Updated last year
- probability of mendelian error in trios.☆11Updated 9 years ago
- Applying IDR analysis to Homer peaks.☆15Updated 5 years ago
- ☆12Updated 8 years ago
- JAMM Peak Finder for Sequencing Datasets☆29Updated 5 years ago
- ☆16Updated last year