Use when working with NGSadmix — admixture estimation from genotype likelihoods. Part of the ANGSD ecosystem; estimates individual ancestry proportions (Q-matrix) from BEAGLE GL files without calling
Use with AI
Install the MCP server or CLI to instantly fetch NGSadmix documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/ngsadmix
dmrseq is an R/Bioconductor package for detecting differentially methylated regions (DMRs) from whole-genome bisulfite sequencing (WGBS) data. It fits a generalized least squares model with a smooth c
1 shared topic • 1 shared operation
IGV (Integrative Genomics Viewer) — high-performance Java desktop application for interactive visualization and exploration of genomic data. Supports BAM/CRAM alignments, VCF variants, BED/GFF annotat
1 shared topic • 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
1 shared topic • 1 shared operation
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
1 shared topic • 1 shared operation
SOAPnuke — C++ quality control and preprocessing tool for high-throughput sequencing data. Filters and trims paired-end or single-end FASTQ reads by adapter content, low quality bases, N-base ratio, r
1 shared topic • 1 shared operation