fengzhanglab / CRISPR-Human_Variation_Nature_Medicine_manuscriptLinks
Code for Scott and Zhang, Nature Medicine manuscript on implications of human genetic variation for therapeutic genome editing
☆8Updated 8 years ago
Alternatives and similar repositories for CRISPR-Human_Variation_Nature_Medicine_manuscript
Users that are interested in CRISPR-Human_Variation_Nature_Medicine_manuscript are comparing it to the libraries listed below
Sorting:
- Comprehensive Human Expressed SequenceS☆17Updated 10 months ago
- A curated list of awesome clonality and tumor heterogeneity resources☆15Updated 6 years ago
- ☆25Updated 4 years ago
- This tool designs guides for use with the base editor technology.☆12Updated last year
- Readme☆10Updated 5 years ago
- Rapid and accurate ancestry inference using SNVs.☆19Updated 2 weeks ago
- RNA-seq analysis scripts☆15Updated last month
- ☆18Updated 5 years ago
- ☆16Updated 8 years ago
- ☆21Updated last year
- R package to detect splicing QTLs (sQTLs)☆15Updated 4 years ago
- Tool package to perform in-silico CRISPR analysis and assessment☆28Updated last year
- Chromatin segmentation in R☆19Updated 7 years ago
- Reconstructs complex variation using Bionano optical mapping data and breakpoint graph data☆17Updated last year
- iread☆24Updated 3 years ago
- Direct RNA publication scripts☆11Updated 7 years ago
- ☆20Updated 8 months ago
- ☆17Updated 11 months ago
- Two pass alignment for long reads☆22Updated 4 years ago
- RNAseq analysis with Hisat2, stringtie, and ballgown☆16Updated 5 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- The code for Daugherty, et al 2017 - Chromatin accessibility dynamics reveal novel functional enhancers in C. elegans☆11Updated 7 years ago
- Analysis pipelines for cancer genome sequencing in mice.☆21Updated 10 months ago
- Using k-mers to call HLA alleles in RNA sequencing data☆22Updated 6 years ago
- A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient☆14Updated 3 weeks ago
- Pipelines for NGS data preprocessing by the Bock lab and friends☆21Updated 2 years ago
- Deprecated, see https://labsyspharm.github.io/rnaseq/☆12Updated 6 years ago
- ☆16Updated last year
- ☆13Updated 2 years ago
- Filters for false-positive mutation calls in NGS☆30Updated 6 years ago