There are 1 repository under cram topic.
VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
Using ChatGPT & GPT-4 to generate CRAM & PyCRAM designators in a one-shot fashion
Rust software for solving impartial games.
Tool for copying read-alignments regions centered around variants (in VCF/VCF.GZ/BCF format) from existing genomes (in SAM/BAM/CRAM format) to insert them into canvas genomes (in SAM/BAM/CRAM format).
Tool for adding genomic variants to an existing genome (in SAM/BAM/CRAM format). Currently supported variants are SNVs, indels and SVs (insertions, deletions, translocations, inversions and duplications). It generates realistic genomes as almost always less than 99% of the original real genome is modified.
Machinekit configuration for the Fabrikator Mini + CRAMPS board
A script to report depth of coverage from BAM/SAM/CRAM file or parse the output generated from "samtools depth"
Convert output from Cram (and some other tools) to TAP (Test Anything Protocol)