ScreenProcessing — Python pipeline for analyzing pooled genetic screens (CRISPRi/CRISPRa). Converts raw FASTQ sequencing files into library counts using fastqgz_to_counts.py, then generates sgRNA phen
Use with AI
Install the MCP server or CLI to instantly fetch ScreenProcessing documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/screenprocessing
Forensic genetics — probabilistic genotyping, STR mixture interpretation, kinship and paternity analysis, population allele frequency databases, and NGS-based forensic sequencing. Covers R packages: f
3 shared topics • 1 shared operation
Use when performing Mendelian randomization (MR) analyses to estimate causal effects of exposures on outcomes using genetic variants as instrumental variables. Covers two-sample MR, IVW, MR-Egger, wei
3 shared topics • 1 shared operation
mpraprofiler — MPRA (Massively Parallel Reporter Assay) data analysis tool for quantifying regulatory element activity from barcode count tables. Normalizes DNA and RNA counts, computes activity ratio
3 shared topics • 1 shared operation
NgsRelate — pairwise relatedness estimation from NGS data using genotype likelihoods. Estimates kinship coefficients, R0/R1/KING-robust statistics, and inbreeding coefficients from VCF/BCF files or AN
3 shared topics • 1 shared operation
TRAPD — Toolkit for Rare variant Association from Population Data. Tests gene-level rare-variant burden in case-control studies using population databases (gnomAD, TOPMed) as controls. Implements adap
3 shared topics • 1 shared operation