ksamocha / de_novo_scriptsLinks
Script used to identify de novo variants from sequencing data.
☆12Updated 8 years ago
Alternatives and similar repositories for de_novo_scripts
Users that are interested in de_novo_scripts are comparing it to the libraries listed below
Sorting:
- An R package for performing MetaSTAAR procedure in whole-genome sequencing studies☆24Updated 10 months ago
- Single Cell Caller (SCcaller) - Identify single nucleotide variations (SNVs) from single cell sequencing data☆35Updated 9 months ago
- ☆17Updated 6 years ago
- A tool to plot significant regions of GWAS☆29Updated 2 years ago
- ☆38Updated 4 years ago
- ☆37Updated 6 years ago
- ☆13Updated 8 years ago
- HiCnv is used to call copy number variations and breakpoints from Hi-C data☆21Updated last year
- ☆15Updated 2 years ago
- Main repository for Drews et al. (Nature, 2022)☆42Updated 2 years ago
- Enhanced version of the FastQTL QTL mapper☆68Updated 2 years ago
- ☆23Updated 4 years ago
- GENome Organisation Visual Analytics☆16Updated 3 years ago
- ☆12Updated 2 years ago
- software for analysis of chromatin feature occupancy profiles from high-throughput sequencing data☆17Updated 5 years ago
- ☆21Updated 6 months ago
- Micro DNA identification☆24Updated 4 years ago
- Fork from https://bitbucket.org/mcgranahanlab/lohhla/src, modified for MSKCC needs☆31Updated 2 years ago
- TEProf2 Pipeline used to find promoters and predict protein sequences from RNA-sequencing data☆27Updated 2 years ago
- ☆21Updated 5 years ago
- ☆23Updated 9 months ago
- A repository containing various scripts useful for performing quality control on data from genome-wide association studies and visualizin…☆20Updated 7 years ago
- The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVOR…☆32Updated 9 months ago
- A comprehensive toolkit for mutational signature analysis☆41Updated last year
- ☆62Updated 3 years ago
- Genomic Association Tester☆32Updated 2 years ago
- An accurate and efficient HLA imputation method.☆26Updated 2 years ago
- ☆22Updated 2 years ago
- RNA editing tests☆17Updated 4 years ago
- A collection of tools to deal with Bisulfite-seq/NOMe-seq (SNP/Methylation calling: BisSNP; HMM segmentation: DMNTools; Visualization/Clu…☆32Updated 3 years ago