nf-core/hic

CNVnator — read-depth (RD) based copy number variation (CNV) detection from whole-genome sequencing BAM/CRAM files. Partitions the genome into equal-size bins, computes normalized read-depth signals,

2 shared topics • 2 shared operations

HiC-Pro is an all-in-one pipeline for processing Hi-C sequencing data from raw FASTQ files to normalized contact matrices. Performs read alignment with Bowtie2, restriction-fragment assignment, valid-

2 shared topics • 2 shared operations

Mondo Disease Ontology — a comprehensive, cross-species disease ontology that harmonizes disease definitions from OMIM, Orphanet, Disease Ontology, NCBI, and other sources into a single unified hierar

2 shared topics • 2 shared operations

Sarek — nf-core Nextflow pipeline for germline and somatic variant calling from whole-genome sequencing (WGS), whole-exome sequencing (WES), and targeted sequencing data. Supports multiple variant cal

2 shared topics • 2 shared operations

vt — C++ command-line variant tool set for manipulating VCF files. Provides variant normalization (left-alignment and trimming), multiallelic decomposition, VCF summary statistics (peek), annotation,

2 shared topics • 2 shared operations